(Q24563491)

English

An enantioselective, modular, and general route to the cytochalasins: synthesis of L-696,474 and cytochalasin B

scientific article

In more languages

edit

Statements

instance of

scholarly article

0 references

title

An enantioselective, modular, and general route to the cytochalasins: synthesis of L-696,474 and cytochalasin B (English)

0 references

1 reference

Andrew M Haidle

1

0 references

Andrew G Myers

series ordinal

2

0 references

language of work or name

English

0 references

publication date

17 August 2004

0 references

published in

Proceedings of the National Academy of Sciences of the United States of America

0 references

volume

101

0 references

issue

33

0 references

page(s)

12048-53

0 references

cites work

Effects of cytochalasin and phalloidin on actin

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514432

retrieved

24 March 2017

Cytochalasin E, an epoxide containing Aspergillus-derived fungal metabolite, inhibits angiogenesis and tumor growth

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514432

retrieved

24 March 2017

L-696,474, a novel cytochalasin as an inhibitor of HIV-1 protease. III. Biological activity

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514432

retrieved

24 March 2017

Microfilaments in Cellular and Developmental Processes

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514432

retrieved

27 September 2017

Allergenic alpha-methylene-gamma-butyrolactones. Study of the capacity of beta-acetoxy- and beta-hydroxy-alpha-methylene-gamma-butyrolactones to induce allergic contact dermatitis in guinea pigs.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514432

retrieved

30 May 2018

Disruption of actin microfilaments by cytochalasin D leads to activation of p53.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1073%2FPNAS.0402111101

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1073%2FPNAS.0402111101

retrieved

21 January 2018

Highly selective hydrolytic kinetic resolution of terminal epoxides catalyzed by chiral (salen)Co(III) complexes. Practical synthesis of enantioenriched terminal epoxides and 1,2-diols

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1073%2FPNAS.0402111101

retrieved

21 January 2018

Acylation through Ketene Intermediates

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1073%2FPNAS.0402111101

retrieved

21 January 2018

Pyridine-derived triflating reagents: An improved preparation of vinyl triflates from metallo enolates

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1073%2FPNAS.0402111101

retrieved

21 January 2018

L-696,474, a novel cytochalasin as an inhibitor of HIV-1 protease. II. Isolation and structure

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15208404

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Synthesis and diastereoselective reactions of n,n-dibenzylamino aldehydes and related compounds

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15208404

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Synthesis of C-protected alpha-amino aldehydes of high enantiomeric excess from highly epimerizable N-protected alpha-amino aldehydes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15208404

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Preparation of Aminoalkyl Chlorohydrin Hydrochlorides: Key Building Blocks for Hydroxyethylamine-Based HIV Protease Inhibitors

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15208404

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Synthesis of the isoindolone nucleus of the cytochalasins

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15208404

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structure of cytochalasins and cytochalasin B binding sites in human erythrocyte membranes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15208404

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

L-696,474, a novel cytochalasin as an inhibitor of HIV-1 protease. I. The producing organism and its fermentation

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15208404

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Proton and carbon-13 nuclear magnetic resonance studies of the conformation of cytochalasin H derivatives and plant growth regulating effects of cytochalasins

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1073%2FPNAS.0402111101

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

DOI

10.1073/PNAS.0402111101

0 references

0 references

0 references

PubMed publication ID

15208404

0 references

ResearchGate publication ID

8500543

0 references

(Q24563491)

An enantioselective, modular, and general route to the cytochalasins: synthesis of L-696,474 and cytochalasin B

Statements

Identifiers

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)