A synthesis of the chlorosulfolipid mytilipin A via a longest linear sequence of seven steps. (Q37329792)

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7 March 2020

title

A synthesis of the chlorosulfolipid mytilipin A via a longest linear sequence of seven steps (English)

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7 March 2020

2

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7 March 2020

author name string

Won-Jin Chung

series ordinal

1

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7 March 2020

D Karl Bedke

series ordinal

3

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7 March 2020

Christopher D Vanderwal

series ordinal

4

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7 March 2020

language of work or name

English

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publication date

8 August 2013

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Angewandte Chemie International Edition

7 March 2020

published in

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7 March 2020

volume

52

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7 March 2020

issue

38

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7 March 2020

page(s)

10052-10055

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α-Haloaldehydes: versatile building blocks for natural product synthesis

7 March 2020

cites work

1 reference

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Concise syntheses of insect pheromones using Z-selective cross metathesis

6 September 2017

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Chelated ruthenium catalysts for Z-selective olefin metathesis

6 September 2017

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Enantioselective dichlorination of allylic alcohols

6 September 2017

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Catalytic Z-selective olefin cross-metathesis for natural product synthesis

6 September 2017

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Chlorosulfolipids: structure, synthesis, and biological relevance

6 September 2017

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A concise enantioselective synthesis of the chlorosulfolipid malhamensilipin A.

6 September 2017

1 reference

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Structure revision and absolute configuration of malhamensilipin A from the freshwater chrysophyte Poterioochromonas malhamensis

6 September 2017

1 reference

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A new class of lipids: chlorosulfolipids

6 September 2017

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Improved ruthenium catalysts for Z-selective olefin metathesis

6 September 2017

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Structural elucidation of a new cytotoxin isolated from mussels of the Adriatic sea.

14 September 2017

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Microbial sulpholipids: (R)-13-chloro-1-(R)-14-docosanediol disulphate and polychlorosulpholipids in Ochromonas danica

28 September 2017

1 reference

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Highly active ruthenium metathesis catalysts exhibiting unprecedented activity and Z-selectivity

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835569

Chlorosulfolipids and the corresponding alcohols from the octocoral Dendronephthya griffini

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835569

Absolute configuration of chlorosulfolipids from the chrysophyta Ochromonas danica.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835569

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

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835569

Enantioselective total synthesis of (-)-napyradiomycin A1 via asymmetric chlorination of an isolated olefin.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835569

Total synthesis of a chlorosulpholipid cytotoxin associated with seafood poisoning

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835569

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

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835569

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

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835569

Theoretical investigation of enolborane addition to alpha-heteroatom-substituted aldehydes. Relevance of the Cornforth and polar Felkin-Anh models for asymmetric induction

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835569

Structure and stereochemistry of a new cytotoxic polychlorinated sulfolipid from Adriatic shellfish

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835569

Enantioselective Ring Opening of Epoxides with Silicon Tetrachloride in the Presence of a Chiral Lewis Base.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835569

Simple and selective method for aldehydes (RCHO) .fwdarw. (E)-haloalkenes (RCH:CHX) conversion by means of a haloform-chromous chloride system

2 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FANIE.201304565

A new cytotoxic polychlorinated sulfolipid from contaminated Adriatic mussels

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FANIE.201304565

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

21 January 2018

1 reference

12 December 2020

Structure of malhamensilipin A, an inhibitor of protein tyrosine kinase, from the cultured chrysophyte Poterioochromonas malhamensis

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.201304565

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23929596%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

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7 March 2020

PubMed publication ID

23929596

1 reference