DSpace at EWHA: Stereoselective synthesis of fluoro-homoneplanocin A as a potential antiviral agent

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DC Field	Value	Language
dc.contributor.author	정낙신	-
dc.date.accessioned	2016-08-28T12:08:16Z	-
dc.date.available	2016-08-28T12:08:16Z	-
dc.date.issued	2012	-
dc.identifier.issn	1523-7060	-
dc.identifier.other	OAK-8696	-
dc.identifier.uri	https://dspace.ewha.ac.kr/handle/2015.oak/222575	-
dc.description.abstract	Fluoro-homoneplanocin A (4) was synthesized from d-ribose, via the enyne ring-closing metathesis of 9, the stereoselective opening of epoxide 23a with fluoride, and a simultaneous oxidation-elimination reaction. The key intermediate 8 is expected to serve as a versatile intermediate for the synthesis of carbanucleosides. © 2012 American Chemical Society.	-
dc.language	English	-
dc.title	Stereoselective synthesis of fluoro-homoneplanocin A as a potential antiviral agent	-
dc.type	Article	-
dc.relation.issue	8	-
dc.relation.volume	14	-
dc.relation.index	SCI	-
dc.relation.index	SCIE	-
dc.relation.index	SCOPUS	-
dc.relation.startpage	2134	-
dc.relation.lastpage	2137	-
dc.relation.journaltitle	Organic Letters	-
dc.identifier.doi	10.1021/ol300667q	-
dc.identifier.wosid	WOS:000302990100047	-
dc.identifier.scopusid	2-s2.0-84860195223	-
dc.author.google	Chandra G.	-
dc.author.google	Majik M.S.	-
dc.author.google	Lee J.Y.	-
dc.author.google	Jeong L.S.	-
dc.contributor.scopusid	정낙신(16028528200)	-
dc.date.modifydate	20211210153610	-