Enantioselective divergent syntheses of several polyhalogenated Plocamium monoterpenes and evaluation of their selectivity for solid tumors. (Q42974807)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25220828%20AND%20SRC:MED&resulttype=core&format=json

16 February 2020

title

Enantioselective divergent syntheses of several polyhalogenated Plocamium monoterpenes and evaluation of their selectivity for solid tumors (English)

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16 February 2020

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3

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16 February 2020

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William H Gerwick

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16 February 2020

author name string

Carl V Vogel

1

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16 February 2020

Halina Pietraszkiewicz

2

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16 February 2020

Frederick A Valeriote

5

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16 February 2020

Christopher D Vanderwal

6

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16 February 2020

language of work or name

English

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publication date

12 September 2014

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Angewandte Chemie International Edition

16 February 2020

published in

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16 February 2020

volume

53

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16 February 2020

issue

45

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16 February 2020

page(s)

12205-12209

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General approach to the synthesis of the chlorosulfolipids danicalipin A, mytilipin A, and malhamensilipin A in enantioenriched form

16 February 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4219742

Approaches to the chemical synthesis of the chlorosulfolipids

26 May 2018

1 reference

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A synthesis of the chlorosulfolipid mytilipin A via a longest linear sequence of seven steps.

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4219742

Enantioselective dichlorination of allylic alcohols

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4219742

Identification and in vitro anti-esophageal cancer activity of a series of halogenated monoterpenes isolated from the South African seaweeds Plocamium suhrii and Plocamium cornutum

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4219742

A concise enantioselective synthesis of the chlorosulfolipid malhamensilipin A.

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4219742

Antiplasmodial halogenated monoterpenes from the marine red alga Plocamium cornutum.

26 May 2018

1 reference

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Stereoselective syntheses of the C(1)-C(9) fragment of amphidinolide C.

26 May 2018

1 reference

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DNA methyl transferase inhibiting halogenated monoterpenes from the Madagascar red marine alga Portieria hornemannii

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4219742

A Three-Step Synthesis of Halomon

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4219742

A pentahalogenated monoterpene from the red alga Portieria hornemannii produces a novel cytotoxicity profile against a diverse panel of human tumor cell lines

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4219742

Discovery and development of anticancer agents from marine sponges: perspectives based on a chemistry-experimental therapeutics collaborative program

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4219742

Relative stereochemistry determination and synthesis of the major chlorosulfolipid from Ochromonas danica.

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4219742

Total synthesis of a chlorosulpholipid cytotoxin associated with seafood poisoning

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4219742

Enantiocontrolled synthesis of polychlorinated hydrocarbon motifs: a nucleophilic multiple chlorination process revisited

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4219742

Stereoselective dichlorination of allylic alcohol derivatives to access key stereochemical arrays of the chlorosulfolipids

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4219742

Allylic 1,3-strain as a controlling factor in stereoselective transformations

16 August 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FANIE.201407726

Synthesis of Undecachlorosulfolipid A: Re-evaluation of the Nominal Structure

21 January 2018

1 reference

12 December 2020

Asymmetric total synthesis of (+)-danicalipin A

1 reference

12 December 2020

Asymmetric total synthesis of danicalipin A and evaluation of biological activity

1 reference

12 December 2020

Asymmetric total synthesis of (+)-hexachlorosulfolipid, a cytotoxin isolated from Adriatic mussels

1 reference

12 December 2020

Identifiers

DOI

10.1002/ANIE.201407726

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25220828%20AND%20SRC:MED&resulttype=core&format=json

16 February 2020

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25220828%20AND%20SRC:MED&resulttype=core&format=json

16 February 2020

1 reference

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