The Laurencia Paradox: An Endless Source of Chemodiversity (Q36068342)

12 August 2017

1 reference

title

The Laurencia Paradox: An Endless Source of Chemodiversity (English)

1 reference

12 August 2017

1 reference

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27380407%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

Vassilios Roussis

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27380407%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

author name string

Maria Harizani

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27380407%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

publication date

1 January 2016

1 reference

Progress in the Chemistry of Organic Natural Products

12 August 2017

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27380407%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

volume

102

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27380407%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

page(s)

91-252

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27380407%20AND%20SRC:MED&resulttype=core&format=json

Natural products as lead structures: chemical transformations to create lead-like libraries.

10 June 2020

cites work

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Halogenated organic molecules of Rhodomelaceae origin: chemistry and biology.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Halogenated compounds from marine algae

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Molecular support for the establishment of the new genus Laurenciella within the Laurencia complex (Ceramiales, Rhodophyta)

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Phylogenetic analyses of theLaurenciacomplex (Rhodomelaceae, Ceramiales) support recognition of five genera:Chondrophycus,Laurencia,Osmundea,PalisadaandYuzuruastat. nov

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Evaluation of impacts of climate change and local stressors on the biotechnological potential of marine macroalgae: a brief theoretical discussion of likely scenarios

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Marine chemical ecology: what's known and what's next?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

TROPHIC BIOLOGY OF STROMBUS GIGAS IN NURSERY HABITATS: DIETS AND FOOD SOURCES IN SEAGRASS MEADOWS

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Transcriptomic analysis of the red seaweed Laurencia dendroidea (Florideophyceae, Rhodophyta) and its microbiome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

The role of vanadium bromoperoxidase in the biosynthesis of halogenated marine natural products

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Exploring the chemistry and biology of vanadium-dependent haloperoxidases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Vanadium bromoperoxidase-catalyzed biosynthesis of halogenated marine natural products

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

An experimental approach to study the biosynthesis of brominated metabolites by the red algal genus Laurencia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Intra-cellular storage, transport and exocytosis of halogenated compounds in marine red alga Laurencia obtusa.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Traffic of secondary metabolites to cell surface in the red alga Laurencia dendroidea depends on a two-step transport by the cytoskeleton

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Induction of halogenated vesicle transport in cells of the red seaweed Laurencia obtusa.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Quantitative GC-ECD analysis of halogenated metabolites: determination of surface and within-thallus elatol of Laurencia obtusa.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

TRANSPORT AND DEFENSIVE ROLE OF ELATOL AT THE SURFACE OF THE RED SEAWEED LAURENCIA OBTUSA (CERAMIALES, RHODOPHYTA)(1).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

An integrated approach using UHPLC-PDA-HRMS and 2D HSQC NMR for the metabolic profiling of the red alga Laurencia: dereplication and tracing of natural products

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Diterpenes, sesquiterpenes, and a C15-acetogenin from the marine red alga Laurencia mariannensis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Halogenated chamigrane sesquiterpenes from Laurencia okamurae.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Sesquiterpenes from the marine red alga Laurencia composita.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Cytotoxic sesquiterpenes from Aplysia dactylomela.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Halogenated diterpenoids from the red alga Laurencia nipponica

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Laurene-type sesquiterpenes from the Red Sea red alga Laurencia obtusa as potential antitumor-antimicrobial agents.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Halogenated metabolites from Japanese Laurencia spp.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Brominated labdane-type diterpenoids from an Okinawan Laurencia sp.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Sesquiterpene and acetogenin derivatives from the marine red alga Laurencia okamurai

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Antileishmanial sesquiterpenes from the Brazilian red alga Laurencia dendroidea.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

New sesquiterpene derivatives from the red alga Laurencia scoparia. Isolation, structure determination, and anthelmintic activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Dactylomelatriol, a biogenetically intriguing omphalane-derived marine sesquiterpene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Sesquiterpenes from the Brazilian red alga Laurencia dendroidea J. Agardh.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Sesquiterpenes and acetogenins from the marine red alga Laurencia okamurai.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Extracts and sesquiterpene derivatives from the red alga Laurencia chondrioides with antibacterial activity against fish and human pathogenic bacteria.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Effect of elatol, isolated from red seaweed Laurencia dendroidea, on Leishmania amazonensis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Dactyloditerpenol acetate, a new prenylbisabolane-type diterpene from Aplysia dactylomela with significant in vitro anti-neuroinflammatory activity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Antibacterial activities of a new brominated diterpene from Borneon Laurencia spp.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Antibacterial activity of halogenated sesquiterpenes from Malaysian Laurencia spp.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Phytochemical studies of the southern Australian marine alga, Laurencia elata.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Sesquiterpenes from the red alga Laurencia tristicha

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Enantioselective synthesis of (+)-majusculone

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Laurane-derived sesquiterpenes from the marine red alga Laurencia tristicha (Rhodomelaceae).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

A seco-laurane sesquiterpene and related laurane derivatives from the red alga Laurencia okamurai Yamada

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

A laurane sesquiterpene and rearranged derivatives from the Chinese red alga Laurencia okamurai Yamada.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Chemical constituents of the red alga Laurencia tristicha

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

A novel brominated cuparene-derived sesquiterpene ether from the red alga Laurencia sp.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Aplysiallene, a new bromoallene as an Na, K-ATPase inhibitor from the sea hare, Aplysia kurodai

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Synthesis and structural revision of (+/-)-laurentristich-4-ol.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Brominated sesquiterpenes from the red alga Laurencia obtusa.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

New bromoterpenes from the red alga Laurencia luzonensis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Terpenoids from Laurencia luzonensis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Sesquiterpenes from Laurencia similis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Metabolites from the sea hare Aplysia fasciata.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Novel stereocontrolled approach to syn- and anti-oxepene-cyclogeranyl trans-fused polycyclic systems: asymmetric total synthesis of (-)-Aplysistatin, (+)-Palisadin A, (+)-Palisadin B, (+)-12-hydroxy-palisadin B, and the AB ring system of adociasulfa

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Synthesis of (+)-luzofuran and (-)-ancistrofuran.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Bisabolanes from the red alga Laurencia scoparia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Cytotoxic halogenated metabolites from the Brazilian red alga Laurencia catarinensis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Aldingenin derivatives from the red alga Laurencia aldingensis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Majapolene A, a cytotoxic peroxide, and related sesquiterpenes from the red alga Laurencia majuscula.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Absolute configurations of brominated sesquiterpenes determined by vibrational circular dichroism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Halogenated sesquiterpenes from the red alga Laurencia obtusa

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Three new sesquiterpenes from the red alga Laurencia perforata.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Halogenated secondary metabolites from Laurencia obtusa.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Brominated metabolites from an Okinawan Laurencia intricata

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

The role of new eudesmane-type sesquiterpenoid and known eudesmane derivatives from the red alga Laurencia obtusa as potential antifungal-antitumour agents

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Red Algae (Rhodophyta) from the Coast of Madagascar: Preliminary Bioactivity Studies and Isolation of Natural Products

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Total synthesis of (.+-.)-poitediol and (.+-.)4-epipoitediol

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Oppositol, a brominated sesquiterpene alcohol of a new skeletal class from the red alga, Laurencia subopposita.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Synthesis of (±)-prepinnaterpene, a bromoditerpene from the red alga Yamada

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Calenzanane sesquiterpenes from the red seaweed Laurencia microcladia from the Bay of Calenzana, Elba Island: acid-catalyzed stereospecific conversion of calenzanol into indene- and guaiazulene-type sesquiterpenes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Aplydactone, a new sesquiterpenoid with an unprecedented carbon skeleton from the sea hare Aplysia dactylomela, and its cargill-like rearrangement.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Halogenated terpenes and a C(15)-acetogenin from the marine red alga Laurencia saitoi.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

New brominated labdane diterpenes from the red alga Laurencia obtusa

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

7-endo radical cyclizations catalyzed by titanocene(III). Straightforward synthesis of terpenoids with seven-membered carbocycles

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Halogenated metabolites from the new Okinawan red alga Laurencia yonaguniensis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Application of a micro multiphase laminar flow on a microchip for extraction and determination of derivatized carbamate pesticides

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Laurenditerpenol, a new diterpene from the tropical marine alga Laurenciaintricata that potently inhibits HIF-1 mediated hypoxic signaling in breast tumor cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Total synthesis of racemic laurenditerpenol, an HIF-1 inhibitor

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Total synthesis and absolute configuration of laurenditerpenol: a hypoxia inducible factor-1 activation inhibitor

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Novel cytotoxic brominated diterpenes from the red alga Laurencia obtusa

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Enantioselective total syntheses of the proposed structures of prevezol B and evaluation of anti-cancer activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Inhibition of sensory afferents activation and visceral pain by a brominated algal diterpene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Thyrsiferol Inhibits Mitochondrial Respiration and HIF-1 Activation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

New polyether triterpenoids from Laurencia viridis and their biological evaluation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Oxasqualenoids from Laurencia viridis: Combined Spectroscopic-Computational Analysis and Antifouling Potential

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Aplysqualenols A and B: Squalene-Derived Polyethers with Antitumoral and Antiviral Activity from the Caribbean Sea Slug Aplysia dactylomela

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Cytotoxic oxasqualenoids from the red alga Laurencia viridis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Studies on polyethers produced by red algae.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Total synthesis of the protein phosphatase 2A inhibitor lactodehydrothyrsiferol

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Omaezallene from red alga Laurencia sp.: structure elucidation, total synthesis, and antifouling activity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

A short total synthesis of (+)-omaezakianol via an epoxide-initiated cationic cascade reaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

A new bromoallene-producing chemical type of the red alga Laurencia nangii masuda.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Beta-hydroxy-gamma-lactones as chiral building blocks for the enantioselective synthesis of marine natural products.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Total synthesis of (2S,3S,5S,10S)-6,9-epoxynonadec-18-ene-7,10-diol and formal total synthesis of (+)-trans-kumausyne from D-arabinose

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Stereochemical determination of five-membered cyclic ether acetogenins using a spin-spin coupling constant approach and DFT calculations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Tetrahydrofuran acetogenins from Laurencia glandulifera

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Laurendecumallenes A-B and laurendecumenynes A-B, halogenated nonterpenoid C(15)-acetogenins from the marine red alga Laurencia decumbens

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Stereostructure assignment of flexible five-membered rings by GIAO 13C NMR calculations: prediction of the stereochemistry of elatenyne

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Structure reassignment of laurefurenynes A and B by computation and total synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Total synthesis and structural revision of laurefurenynes A and B.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Bioactive C15 acetogenins from the red alga Laurencia obtusa.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

A general strategy for construction of both 2,6-cis- and 2,6-trans-disubstituted tetrahydropyrans: substrate-controlled asymmetric total synthesis of (+)-scanlonenyne.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Total synthesis of (-)-laurenyne. Use of acetal-initiated cyclizations to prepare functionalized eight-membered cyclic ethers

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Brasilenyne and cis-dihydrorhodophytin: Antifeedant medium-ring haloethers from a sea hare (Aplysia brasiliana).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Formal total syntheses of (+)-prelaureatin and (+)-laurallene by diastereoselective brook rearrangement-mediated [3 + 4] annulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Expedient enantioselective synthesis of the δ4-oxocene cores of (+)-laurencin and (+)-prelaureatin (‡).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

C(15) Acetogenins from the red alga Laurencia obtusa

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Nonterpenoid C15 acetogenins from Laurencia marilzae

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

An enantioselective approach to (+)-laurencin

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

An approach to lauroxanes by iterative use of Co(2)(CO)(6)-acetylenic complexes. a formal synthesis of (+)-laurencin

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Palladium-Catalyzed Medium-Ring Formation for Construction of the Core Structure of Laurencia Oxacycles: Synthetic Study of Laurendecumallene B

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Toward a formal synthesis of laureatin: unexpected rearrangements involving cyclic ether nucleophiles

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

(3Z)-Bromofucin from a South African sea hare.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Substrate-controlled asymmetric total synthesis of (+)-microcladallene B with a bromination strategy based on a nucleophile-assisting leaving group.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Intramolecular silicon-assisted cross-coupling: total synthesis of (+)-brasilenyne

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Total synthesis of (+)-brasilenyne. Application of an intramolecular silicon-assisted cross-coupling reaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Enantioselective total synthesis of (+)-obtusenyne

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Synthesis of (+)-obtusenyne

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Asymmetric total synthesis of (-)-isolaurallene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Substrate-controlled asymmetric total synthesis and structure revision of (+)-itomanallene A.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

A biosynthetically-inspired synthesis of the tetrahydrofuran core of obtusallenes II and IV.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

A hypothesis concerning the biosynthesis of the obtusallene family of marine natural products via electrophilic bromination.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Sulfur-containing polybromoindoles from the Formosan red alga Laurencia brongniartii

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Syntheses of polybrominated indoles from the red alga Laurencia brongniartii and the brittle star Ophiocoma erinaceus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Antimalarial activity: the search for marine-derived natural products with selective antimalarial activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Red algal bromophenols as glucose 6-phosphate dehydrogenase inhibitors

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Highly brominated metabolites from marine red alga Laurencia similis inhibit protein tyrosine phosphatase 1B.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

24-Branched Δ5 sterols from Laurencia papillosa red seaweed with antibacterial activity against human pathogenic bacteria

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

A new antitumor arabinopyranoside from Laurencia majuscula induces G2/M cell cycle arrest

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Inhibitors of oxidation and matrix metalloproteinases, floridoside, and D-isofloridoside from marine red alga Laurencia undulata

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Total synthesis of marine eicosanoid (-)-hybridalactone.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Impact of natural products on developing new anti-cancer agents

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Dactylone inhibits epidermal growth factor-induced transformation and phenotype expression of human cancer cells and induces G1-S arrest and apoptosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Aplysin sensitizes cancer cells to TRAIL by suppressing P38 MAPK/survivin pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Laurencia okamurai extract containing laurinterol induces apoptosis in melanoma cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Assessment of antimycobacterial activity of a series of mainly marine derived natural products

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Cytotoxic activity of semi-synthetic derivatives of elatol and isoobtusol.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Anti-tumour effects of elatol, a marine derivative compound obtained from red algae Laurencia microcladia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Parguerenes: Marine red alga bromoditerpenes as inhibitors of P-glycoprotein (ABCB1) in multidrug resistant human cancer cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Bioactive brominated diterpenes from the marine red alga Jania Rubens (L.) Lamx.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Thyrsiferyl 23-acetate is a novel specific inhibitor of protein phosphatase PP2A.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Thyrsiferyl 23-acetate and its derivatives induce apoptosis in various T- and B-leukemia cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Induction of apoptosis in estrogen dependent and independent breast cancer cells by the marine terpenoid dehydrothyrsiferol.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Chemical modulation of VLA integrin affinity in human breast cancer cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

The inhibitory effects of squalene-derived triterpenes on protein phosphatase PP2A.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

7,11-epi-thyrsiferol: completion of its synthesis, evaluation of its antimitotic properties, and the further development of an SAR model

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Aplysqualenol A binds to the light chain of dynein type 1 (DYNLL1).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Pharmacophore modeling for qualitative prediction of antiestrogenic activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Potent antibacterial activity of halogenated metabolites from Malaysian red algae, Laurencia majuscula (Rhodomelaceae, Ceramiales).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Potent antibacterial activity of halogenated compounds against antibiotic-resistant bacteria.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Antimicrobial Agents from Marine Algae

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Natural products as antiparasitic drugs.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

In vitro anti-trypanosomal activity of elatol isolated from red seaweed Laurencia dendroidea

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Trypanocidal action of (-)-elatol involves an oxidative stress triggered by mitochondria dysfunction.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Additional evidence of the trypanocidal action of (-)-elatol on amastigote forms through the involvement of reactive oxygen species

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Inhibitory activity of marine sponge-derived natural products against parasitic protozoa

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Recent developments in anti-inflammatory natural products

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Assessment of anti-inflammatory effect of 5β-hydroxypalisadin B isolated from red seaweed Laurencia snackeyi in zebrafish embryo in vivo model

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

In vivo and in vitro anti-inflammatory activity of neorogioltriol, a new diterpene extracted from the red algae Laurencia glandulifera

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Floridoside suppresses pro-inflammatory responses by blocking MAPK signaling in activated microglia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Marine natural products as acetylcholinesterase inhibitor: comparative quantum mechanics and molecular docking study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

New drug metabolism inhibitor of marine origin

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Chemical Defense Against Diverse Coral-Reef Herbivores

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Ecological roles of natural products of the Brazilian red seaweed Laurencia obtusa.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Mini-review: Inhibition of biofouling by marine microorganisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Synthesis of the Proposed Structures of Prevezol C

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Towards the synthesis of prevezol C: total enantioselective synthesis of (−)-2-epi-prevezol C

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Inhibition of coral recruitment by macroalgae and cyanobacteria

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

The stereochemistry and biosynthesis of hybridalactone, an eicosanoid from

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

New Halogenated Sesquiterpenes from South African Specimens of the Circumtropical Sea HareAplysiadactylomela

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Absolute Stereochemistry of Ibhayinol from a South African Sea Hare

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Structure revision of okamurallene and structure elucidation of further C15 non-terpenoid bromoallenes from Laurencia intricata

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Isolation of elatol from Laurencia microcladia and its palatability to the sea urchin Echinometra lucunter

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

New laurene derivatives from Laurencia filiformis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Sesquiterpenes from the essential oil of Laurencia dendroidea (Ceramiales, Rhodophyta): isolation, biological activities and distribution among seaweeds

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Aplysiols C - E, Brominated Triterpene Polyethers from the Marine Alga Chondria armata and a Revision of the Structure of Aplysiol B

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Calenzanol, the first member of a new class of sesquiterpene with a novel skeleton isolated from the red seaweed Laurencia microcladia from the Bay of Calenzana, Elba Island

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

21 January 2018

Marine natural products

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Volatile halogenated metabolites from marine red algae

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Osmundea lata (M. Howe & W.R. Taylor)comb. nov. (Ceramiales, Rhodophyta) from the Brazilian south-eastern continental shelf

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Ultrastructure of the parasite Janczewskia morimotoi and its host Laurencia nipponica (ceramiales, rhodophyta)

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

New natural product isolation and comparison of the secondary metabolite content of three distinct samples of the sea hare Aplysia dactylomela from tenerife

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

(E)-2-Tridecyl-2-heptadecenal, an Unusual Metabolite from the Red AlgaLaurenciaSpecies

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Halogenated metabolites with antibacterial activity from the Okinawan Laurencia species

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Effects of abiotic factors on growth and chemical defenses in cultivated clones of Laurencia dendroidea J. Agardh (Ceramiales, Rhodophyta)

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

The absolute configurations of halogenated chamigrene derivatives from the marine alga, laurencia glandulifera kützing

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Epilaurallene, a New Nonterpenoid C15-Bromoallene from the Red AlgaLaurencia nipponicaYamada

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

(5S,7R,10R)-selin-4(14)-en-5α-ol, a sesquiterpene alcohol from the red alga Laurencia nipponica

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Laurencia rigida: chemical investigations of its antifouling dichloromethane extract

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Halogenated Sesquiterpenes from the Marine Red AlgaLaurencia saitoi(Rhodomelaceae)

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Sesquiterpenes from Laurencia claviformis

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Chemical Relationships between the Sea Hare Aplysia parvula and the Red Seaweed Laurencia filiformis from Tasmania

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

A New Chamigrane from Laurencia glomerata

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

New Sesquiterpenes and C15Acetogenins from the Marine Red Alga Laurencia implicata

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Fourteen Chamigrane Derivatives from a Red Alga,Laurencia nidifica

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Six New Sesquiterpenoids from the Red AlgaLaurencia nipponicaYamada

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Chamigrane metabolites from Laurencia obtusa and L. scoparia

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

New C15Acetogenins and Sesquiterpenes from the Red Alga Laurencia sp. cf. L. gracilis

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Structures and chemistry of two new halogen-containing chamigrene derivatives from laurencia

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

A New C15Acetogenin from the Marine AlgaLaurencia claviformis

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

The Structure and Absolute Stereochemistry of a Halogenated Chamigrene Derivative from the Red AlgaLaurenciaSpecies

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Chemical variation in a new bromochamigrene derivative from the red seaweed Laurencia pacifica

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Structures of Halogenated Chamigrene Derivatives, Minor Constituents from the Red AlgaLaurencia nipponicaYamadan

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Tropical Marine Algae, VII. The Chemical Composition of Marine Algae from North Queensland Waters

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Majusculone, a Novel Norchamigrane-Type Metabolite from the Red AlgaLaurencia majusculaHarvey

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Chamigrane metabolites from a Jamaican variety of laurencia obtusa

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Sesquiterpenes from Laurencia spp.

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Evidence for the biogenesis of halogenated chamigrenes from the red alga laurencia obtusa

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Two New Chamigrene Sesquiterpenoids from the Tropical Red Alga Laurencia obtusa

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Metabolites from Laurencia obtusa

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Chamigrenelactone, a polyoxygenated sesquiterpene with a novel structural type and devoid of halogen from Laurencia obtusa

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

The Structure of Notoryne, a Halogenated C15Nonterpenoid with a Novel Carbon Skeleton from the Red AlgaLaurenda nipponicaYamada

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Oxachamigrenes, new halogenated sesquiterpenes from Laurencia obtusa

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Two new chamigranes from an hawaiian red alga, Laurencia cartilaginea

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Cartilagineol, the fourth lineage of Laurencia-derived polyhalogenated chamigrene

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Four new chamigrane sesquiterpenoids from the opistobranch mollusk Aplysia dactylomela

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Three halogenated metabolites fromLaurencia obtusa

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Ma'iliohydrin, a cytotoxic chamigrene dibromohydrin from a Philippine Laurencia species

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Two metabolites from the red alga Laurencia flexilis

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Tropical Marine Algae. VIII. The Structural Determination of Novel Sesquiterpenoid Metabolites From the Red Alga .Laurencia majuscula

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Marine natural products: parguerol, deoxyparguerol, and isoparguerol. New brominated diterpenes with modified pimarane skeletons from the sea hare Aplysia dactylomela

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Tropical Marine Algae. III. New Sesquiterpenes From Laurencia majuscula (Rhodophyta, Rhodophyceae, Ceramiales, Rhodomelaceae)

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

X-Ray Structure Determination of (−)-Obtusane, a New Sesquiterpene from the Red Alga,Laurencia nipponicaYamada

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Terpenes and Polybromoindoles from the Marine Red AlgaLaurencia decumbens (Rhodomelaceae)

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Carbon-13 NMR application to Laurencia polyhalogenated sesquiterpenes

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

C15 acetogenins and terpenes of the dictyoceratid sponge Spongia zimocca of Il Rogiolo: A case of seaweed-metabolite transfer to, and elaboration within, a sponge?

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Antibacterial halogenated metabolites from the Malaysian Laurencia species

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

New cytotoxic halogenated sesquiterpenes from the Egyptian sea hare, Aplysia oculifera

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Enantioselective ring construction: synthesis of halogenated marine natural spiro[5.5]undecane sesquiterpenes

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Structures of Two New Halochamigrene Derivatives from the Red AlgaLaurencia nipponicaYamada

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Halogenated sesquiterpenoids from the Hawaiian marine alga Laurencia nidifica. II. Nidifidienol

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Sesquiterpenoids of Laurencia majuscula (Ceramiales, Rhodophyta) from the Ryukyu Islands, Japan

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

The Absolute Configurations and Biogenesis of Some New Halogenated Chamigrenes from the Sea HareAplysia dactylomela

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Marine Natural Products; VI. A Halogenated Chamigrene Epoxide from the Red Alga Laurencia pinnatifida

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

A rearranged chamigrene derivative and its potential biogenetic precursor from a new species of the marine red algal genus Laurencia (rhodomelaceae)

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Some chemical constituents of the digestive gland of the sea hare Aplysia californica

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Elatenyne—a Pyrano[3,2-B]Pyranyl Vinyl Acetylene From the Red Alga Laurencia elata

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Tropical Marine Algae. IX. A New Sesquiterpenoid Metabolite From the Red Alga Laurencia marianensis

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

A New Chamigrane-type Bromo Diether from the Red AlgaLaurencia nipponicaYamada

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Marine natural products. IV. Prepacifenol, a halogenated epoxy sesquiterpene and precursor to pacifenol from the red alga, Laurencia filiformis

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

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1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

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1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

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1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

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1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

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1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

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1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

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1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

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1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

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1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

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1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

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1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

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1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

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1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

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1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

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1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

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1 reference

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1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

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1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

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1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

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1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

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1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

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1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

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1 reference

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1 reference

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https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

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https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

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https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

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1 reference

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https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

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https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Chemical constituents of Chondrophycus papillosus and their cytotoxicity in vitro

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https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

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https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

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1 reference

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1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

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https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

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https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

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1 reference

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1 reference

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Parguerol and Isoparguerol Isolated from the Sea Hare, Aplysia kurodai, Induce Neurite Outgrowth in PC-12 Cells

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Neorogioltriol: A brominated diterpene with analgesic activity from Laurencia glandulifera

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Laurencianol, a new halogenated diterpenoid from the marne alga

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Glandulaurencianols A–C, brominated diterpenes from the red alga, Laurencia glandulifera and the sea hare, Aplysia punctata

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Kahukuenes, new diterpenoids from the marine alga Laurencia majuscula

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Aplysiadiol, a New Brominated Diterpene from the Marine Mollusc Aplysia kurodai

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Highly Oxygenated Triterpenoids from the Marine Red AlgaLaurencia mariannensis(Rhodomelaceae)

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Teurilene and thyrsiferyl 23-acetate, meso and remarkably cytotoxic compounds from the marine red alga laurencia obtusa (hudson) lamouroux

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Venustatriol. A new, anti-viral, triterpene tetracyclic ether from Laurencia venusta

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Evaluation of the cytotoxic activity of polyethers isolated from Laurencia

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Aplysiols A and B, squalene-derived polyethers from the mantle of the sea hare Aplysia dactylomela

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

New polyether squalene derivatives from Laurencia

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Cytotoxic Squalene-Derived Polyethers from the Marine Red AlgaLaurencia obtusa(Hudson) Lamouroux

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Several new squalene-derived triterpenes from Laurencia

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Thyrsenols A and B, two unusual polyether squalene derivatives

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Total synthesis of pseudodehydrothyrsiferol

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Aurilol, a Cytotoxic Bromotriterpene Isolated from the Sea HareDolabella auricularia

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Total synthesis and complete assignment of the stereostructure of a cytotoxic bromotriterpene polyether (+)-aurilol

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Assignment of the absolute configuration of the marine pentacyclic polyether (+)-enshuol by total synthesis

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Epoxide-opening cascades triggered by a Nicholas reaction: total synthesis of teurilene

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Intricatetraol, a halogenated triterpene alcohol from the red alga Laurencia intricata

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Total synthesis and determination of the absolute configuration of (+)-intricatetraol

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Auriculol, a cytotoxic oxygenated squalene from the Japanese sea hare Dolabella auricularia: isolation, stereostructure, and synthesis

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Marine polyether triterpenes

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Graciosin and graciosallene, two bromoethers from Laurencia obtusa

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Three new bromo ethers from the red alga laurencia obtusa

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

KUMAUSYNES AND DEACETYLKUMAUSYNES, FOUR NEW HALOGENATED C-15 ACETYLENES FROM THE RED ALGALAURENCIA NIPPONICAYAMADA

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

A total synthesis of (+/-)-trans-kumausyne

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Bisezakyne-A and -B, halogenated C15 acetogenins from a Japanese Laurencia species

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Laureepoxide, new bromo ether from the marine red alga Laurencia nipponica Yamada

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Total synthesis and structure confirmation of elatenyne: success of computational methods for NMR prediction with highly flexible diastereomers

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Lauroxolanes from the marine alga Laurencia majuscula

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

The changing faces of halogenated marine natural products: total synthesis of the reported structures of elatenyne and an enyne from Laurencia majuscula

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Synthesis of the originally proposed structures of elatenyne and an enyne from Laurencia majuscula

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Laurefurenynes A–F, new Cyclic Ether Acetogenins from a Marine Red Alga, Laurencia sp.

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

KUMAUSALLENE, A NEW BROMOALLENE FROM THE MARINE RED ALGALAURENCIA NIPPONICAYAMADA

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Enantioselective Total Synthesis of the Nonisoprenoid Sesquiterpene (−)-Kumausallene

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Stereoselective total synthesis of (-)-kumausallene

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

First total synthesis and structural reassignment of (-)-aplysiallene

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

The Absolute Stereochemistry of Okamurallene and Its Congeners, Halogenated C15Nonterpenoids from the Red AlgaLaurencia intricata

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

DEOXYOKAMURALLENE AND ISOOKAMURALLENE, NEW HALOGENATED NONTERPENOID C15-COMPOUNDS FROM THE RED ALGALAURENCIA OKAMURAIYAMADA

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Panacene: An aromatic bromoallene from a sea hare (Aplysia brasiliana)

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Expeditious total syntheses of natural allenic products via aromatic ring umpolung

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Laurenidificin, a new brominated C15-acetogenin from the marine red alga Laurencia nidifica

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Two bicyclic C15 enynes from the sea hare Aplysia oculifera

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Marine natural products: isodactylyne, a halogenated acetylenic ether from the sea hare Aplysia dactylomela

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Marine natural products. Dactylyne, an acetylenic dibromochloro ether from the sea hare Aplysia dactylomela

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Srilankenyne, a new metabolite from the sea hare Aplysia oculifera

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

β-Hydroxy-γ-lactones as nucleophiles in the Nicholas reaction for the synthesis of oxepene rings. Enantioselective formal synthesis of (-)-isolaurepinnacin and (+)-rogioloxepane A

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

On the unusual propensity by the red seaweedLaurencia microcladia of II Rogiolo to form C15 oxepanes: Isolation of rogioloxepane A, B, C, and their likely biogenetic acyclic precursor, prerogioloxepane

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Enantioselective total synthesis of (+)-rogioloxepane A

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Structures and absolute stereochemistry of nipponallene and neonipponallene, new brominated allenes from the red alga Laurencia nipponica

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Rogiolenyne D, the likely immediate precursor of rogiolenyne A and B, branched C15 acetogenins isolated from the red seaweedLaurencia microcladia of II Rogiolo. Conformation and absolute configuration in the whole series

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Rogiolenyne A, B, and C: The First Branched Marine C15 Acetogenins. Isolation from the Red SeaweedLaurencia microcladia or the SpongeSpongia zimocca of II Rogiolo

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Novel "protecting group-dependent" alkylation-RCM strategy to medium-sized oxacycles: first total synthesis of --isoprelaurefucin

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Neoisoprelaurefucin, a halogenated C15 non-terpenoid compound from Laurencia nipponica

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Laurenyne, a new acetylene from Laurencia obtusa: crystal structure and absolute configuration

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Two C15 bromoallenes from the red alga Laurencia obtusa

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Synthetic and mechanistic studies of the retro-Claisen rearrangement. 4. An application to the total synthesis of (+)-Laurenyne

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Stereoselective synthesis of the cyclic ether core of (+)-laurenyne

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

THE STRUCTURES OF (3Z)-EPOXYVENUSTIN, (3Z)-VENUSTIN, AND (3Z)-VENUSTINENE, NEW HALOGENATED C15-NONTERPENOIDS FROM THE RED ALGALAURENCIA VENUSTAYAMADA

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Rhodophytin, a halogenated vinyl peroxide of marine origin

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

VENUSTIN A AND B, NEW HALOGENATED C15METABOLITES FROM THE RED ALGALAURENCIA VENUSTAYAMADA

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

E-Dihydrorhodophytin, A C15 acetogenin from the red alga Laurencia pinnatifida

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Prelaureatin, a new biogenetic key intermediate isolated from Laurencia nipponica

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Non-terpenoid C-15 metabolites from the red seaweed Laurencia pinnatifida

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Construction of eight-membered ether rings by olefin geometry-dependent internal alkylation: first asymmetric total syntheses of (+)-3-(E)- and (+)-3-(Z)-pinnatifidenyne

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Concise synthetic approaches for the Laurencia family: formal total syntheses of (±)-laurefucin and (±)-E- and (±)-Z-pinnatifidenyne

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Doliculols A and B, the non-halogenated C15 acetogenins with cyclic ether from the sea hare Dolabella auricularia

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Laurencin, a constituent of Laurencia glandulifera Kützing

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Synthesis of Medium Ring Ethers. 5. The Synthesis of (+)-Laurencin

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Total synthesis of (+)-laurencin: an asymmetric alkylation-ring-closing metathesis approach to medium ring ethers

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Highly stereoselective and efficient total synthesis of (+)-laurencin

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Metabolites of the marine red alga Laurencia thyrsifera. III

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Secondary metabolites from the red alga Laurenciaintricata: halogenated enynes

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Asymmetric Total Synthesis of (+)-Bermudenynol, a C15LaurenciaMetabolite with a Vinyl Chloride Containing Oxocene Skeleton, through Intramolecular Amide Enolate Alkylation

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

C15 acetogenins with antistaphylococcal activity from the red alga Laurencia glandulifera

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

A new vinyl acetylene from the red alga Laurencia thyrsifera

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Three new vinyl acetylenes from the marine red alga laurencia

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Concise Substrate-Controlled Asymmetric Total Syntheses of Dioxabicyclic Marine Natural Products with 2,10-Dioxabicyclo-[7.3.0]dodecene and 2,9-Dioxabicyclo[6.3.0]undecene Skeletons

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Pannosallene, a brominated C15 nonterpenoid from Laurencia pannosa

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

(3E)-Laureatin and (3E)-Isolaureatin, Halogenated C-15 Non-Terpenoid Compounds from the Red AlgaLaurencia nipponicaYamada

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Laureatin and isolaureatin, constituents of Laurencia nipponica Yamada

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Asymmetric total syntheses of (+)-3-(z)-laureatin and (+)-3-(z)-isolaureatin by "lone pair-lone pair interaction-controlled" isomerization

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Structure elucidation of laureoxanyne, a new nonisoprenoid C15 enyne, using lactoperoxidase

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Bromoallenes from the alga Laurencia microcladia

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Total Synthesis of (+)-Obtusenyne

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

ISOLAURALLENE, A NEW NONTERPENOID C15-BROMOALLENE, FROM THE RED ALGALAURENCIA NIPPONICAYAMADA

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Twelve-MemberedO-Bridged Cyclic Ethers of Red Seaweeds in the GenusLaurencia Exist in Solution as Slowly Interconverting Conformers

31 March 2020

1 reference

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Dactylallene: A novel dietary C15 bromoallene from the Atlantic anaspidean mollusc Aplysia dactylomela

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Bromonium ion induced transannular oxonium ion formation-fragmentation in model obtusallene systems and structural reassignment of obtusallenes V-VII

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

A new and highly oxygenated bromoallene from a marine source.

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Obtusallene I, a new halogenated allene from Laurencia Obtusa

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

A new haloether from Laurencia possessing a lauroxacyclododecane ring. Structural and conformational studies

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

New bicyclotridecane C15 nonterpenoid bromoallenes from Laurencia marilzae

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Poitediene a new metabolite from the marine red alga

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Biogenetic intermediates, (3e and 3z,12z)-laurediols and (3e and 3z)-12,13- dihydrolaurediols, isolated from Laurencia nipponica

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Efficient syntheses of trans-(+)-laurediol from carbohydrate precursors

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Structural reassignment of obtusallenes V, VI, and VII by GIAO-based density functional prediction

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Synthesis of bromoindole alkaloids from Laurencia brongniartii

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Sulfur-containing polybromoindoles from the red alga Laurencia brongniartii

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Itomanindoles A and B. Methylsulfinylindoles from Laurencia Brongniartii

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Five New Sulfur-containing Polybrominated Bisindoles from the Red Alga Laurencia brongniartii

31 March 2020

1 reference

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Ecdysone-like metabolites, 14α-hydroxypinnasterols, from the red alga Laurencia pinnata

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Marine sterols. 23. 2a-oxa-2-oxo-5α-hydroxy-3,4-dinorcholestane from the arabian sea red alga laurencia obtusa

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Laurencione, a heterocycle from the red alga Laurencia spectabilis

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Sphingosine derivatives from red algae of the ceramiales

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Hybridalactone, An unusual fatty acid metabolite from the red alga Laurencia hybrida (Rhodophyta, Rhodomelaceae)

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Catalysis-Based and Protecting-Group-Free Total Syntheses of the Marine Oxylipins Hybridalactone and the Ecklonialactones A, B, and C

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Papillamide, a Novel Fatty Acid Amide from the Red AlgaLaurencia papillosa

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Antimicrobial components of the red alga Laurencia hybrida (Rhodophyta, Rhodomelaceae)

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Isolation of 12-(S)-hepe from the red marine alga murrayella periclados and revision of structure of an acyclic icosanoid from laurencia hybrida. Implications to the biosynthesis of the marine prostanoid hybridalactone

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

31 March 2020

1 reference

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Squalene derivatives from Eurycoma longifolia

31 March 2020

1 reference

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Protective effect of Aplysin on hepatic injury in ethanol-treated rats

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Brine shrimp: a convenient general bioassay for active plant constituents

31 March 2020

1 reference

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The development of a marine natural product-based antifouling paint

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

The need for standardised broad scale bioassay testing: A case study using the red alga Laurencia rigida

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-319-33172-0_2

Novel Lactone Chamigrene-Derived Metabolites fromLaurencia majuscula

31 March 2020

1 reference

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Cuparene-Derived Sesquiterpenes from the Chinese Red AlgaLaurencia okamurai Yamada

1 reference

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Aristolane Sesquiterpenes and Highly Brominated Indoles from the Marine Red AlgaLaurencia similis (Rhodomelaceae)

1 reference

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Identifiers

DOI

10.1007/978-3-319-33172-0_2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27380407%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

1 reference