Structure reassignment of laurefurenynes A and B by computation and total synthesis (Q34795221)

4 August 2017

Structure reassignment of laurefurenynes A and B by computation and total synthesis (English)

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4 August 2017

4

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4 August 2017

Phillip A Broadwith

2

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author name string

David J Shepherd

series ordinal

1

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4 August 2017

Bryony S Dyson

series ordinal

3

1 reference

4 August 2017

Jonathan W Burton

series ordinal

5

1 reference

4 August 2017

language of work or name

English

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publication date

21 August 2013

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Chemistry—A European Journal

4 August 2017

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4 August 2017

19

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4 August 2017

38

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4 August 2017

12644-12648

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

4 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4280896

Long-range corrected hybrid density functionals with damped atom-atom dispersion corrections

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4280896

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4280896

Determination of relative configuration in organic compounds by NMR spectroscopy and computational methods.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4280896

Prevention of undesirable isomerization during olefin metathesis

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4280896

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

8 July 2018

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201302349

Leiodermatolide, a potent antimitotic macrolide from the marine sponge Leiodermatium sp.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201302349

First natural analogs of the cytotoxic thiodepsipeptide thiocoraline A from a marine Verrucosispora sp.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201302349

Prediction of the structure of nobilisitine a using computed NMR chemical shifts

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201302349

Case study of empirical and computational chemical shift analyses: reassignment of the relative configuration of phomopsichalasin to that of diaporthichalasin

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201302349

Peptidolipins B-F, antibacterial lipopeptides from an ascidian-derived Nocardia sp.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201302349

Enantioselective total synthesis of (+)-obtusenyne

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201302349

The osmium-catalyzed asymmetric dihydroxylation: a new ligand class and a process improvement

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201302349

Determination of the relative stereochemistry of flexible organic compounds by Ab initio methods: conformational analysis and Boltzmann-averaged GIAO 13C NMR chemical shifts.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201302349

Computational prediction of 1H and 13C chemical shifts: a useful tool for natural product, mechanistic, and synthetic organic chemistry

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201302349

Merck molecular force field. I. Basis, form, scope, parameterization, and performance of MMFF94

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201302349

Biomimetic asymmetric total synthesis of (-)-laurefucin via an organoselenium-mediated intramolecular hydroxyetherification

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201302349

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201302349

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/10.1002%2FCHEM.201302349

Total synthesis and structural revision of laurefurenynes A and B.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4280896

Relative stereochemical determination and synthesis of the C17-C25 δ-lactone fragment of hemicalide

26 October 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

Assigning stereochemistry to single diastereoisomers by GIAO NMR calculation: the DP4 probability

1 reference

12 December 2020

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

1 reference

12 December 2020

Structure validation of natural products by quantum-mechanical GIAO calculations of 13C NMR chemical shifts

1 reference

12 December 2020

A unifying stereochemical analysis for the formation of halogenated C15-acetogenin medium-ring ethers from Laurencia species via intramolecular bromonium ion assisted epoxide ring-opening and experimental corroboration with a model epoxide

1 reference

12 December 2020

A general strategy for the stereocontrolled preparation of diverse 8- and 9-membered Laurencia-type bromoethers

1 reference

12 December 2020

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

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1246/BCSJ.64.1763

Identifiers

DOI

10.1002/CHEM.201302349

1 reference

4 August 2017

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4 August 2017

1 reference