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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.identifier http://www.ncbi.nlm.nih.gov/pubmed/20491466
dc.identifier.uri https://hdl.handle.net/10161/4106
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.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.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.id Hong, Jiyong|0375024
dc.description.version Version of Record
duke.date.pubdate 2010-6-18
duke.description.issue 12
duke.description.volume 12
dc.relation.journal Organic letters
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
dc.identifier.eissn 1523-7052
duke.contributor.orcid Hong, Jiyong|0000-0002-5253-0949


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