Total synthesis of cyanolide A and confirmation of its absolute configuration.

dc.contributor.author

Kim, Hyoungsu

dc.contributor.author

Hong, Jiyong

dc.coverage.spatial

United States

dc.date.accessioned

2011-06-21T17:27:10Z

dc.date.issued

2010-06-18

dc.description.abstract

The tandem allylic oxidation/oxa-Michael reaction promoted by the gem-disubstituent effect and the 2-methyl-6-nitrobenzoic anhydride (MNBA)-mediated dimerization were explored for the efficient and facile synthesis of cyanolide A.

dc.description.version

Version of Record

dc.identifier

http://www.ncbi.nlm.nih.gov/pubmed/20491466

dc.identifier.eissn

1523-7052

dc.identifier.uri

https://hdl.handle.net/10161/4106

dc.language

eng

dc.language.iso

en_US

dc.publisher

American Chemical Society (ACS)

dc.relation.ispartof

Org Lett

dc.relation.isversionof

10.1021/ol101022z

dc.relation.journal

Organic letters

dc.subject

Anhydrides

dc.subject

Animals

dc.subject

Glycosylation

dc.subject

Macrolides

dc.subject

Molecular Structure

dc.subject

Nitrobenzoates

dc.subject

Oxidation-Reduction

dc.subject

Schistosoma

dc.title

Total synthesis of cyanolide A and confirmation of its absolute configuration.

dc.title.alternative
dc.type

Journal article

duke.contributor.orcid

Hong, Jiyong|0000-0002-5253-0949

duke.date.pubdate

2010-6-18

duke.description.issue

12

duke.description.volume

12

pubs.author-url

http://www.ncbi.nlm.nih.gov/pubmed/20491466

pubs.begin-page

2880

pubs.end-page

2883

pubs.issue

12

pubs.organisational-group

Basic Science Departments

pubs.organisational-group

Chemistry

pubs.organisational-group

Duke

pubs.organisational-group

Duke Cancer Institute

pubs.organisational-group

Institutes and Centers

pubs.organisational-group

Pharmacology & Cancer Biology

pubs.organisational-group

School of Medicine

pubs.organisational-group

Trinity College of Arts & Sciences

pubs.publication-status

Published

pubs.volume

12

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