DSpace at EWHA: Synthesis of fluoroneplanocin A

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DC Field	Value	Language
dc.contributor.author	정낙신	-
dc.contributor.author	최원준	-
dc.date.accessioned	2016-08-28T11:08:55Z	-
dc.date.available	2016-08-28T11:08:55Z	-
dc.date.issued	2008	-
dc.identifier.issn	1934-9270	-
dc.identifier.other	OAK-13186	-
dc.identifier.uri	https://dspace.ewha.ac.kr/handle/2015.oak/229217	-
dc.description.abstract	Fluoroneplanocin A, designed as a potent mechanism-based irreversible inhibitor of S-adenosylhomocysteine hydrolase (SAH), is synthesized from D-ribose via a key D-cyclopentenone intermediate. This intermediate is synthesized using a stereoselective Grignard reaction, a ring-closing metathesis (RCM) reaction, and oxidative rearrangement as key steps. © 2008 by John Wiley & Sons, Inc.	-
dc.language	English	-
dc.title	Synthesis of fluoroneplanocin A	-
dc.type	Review	-
dc.relation.issue	SUPPL. 34	-
dc.relation.index	SCOPUS	-
dc.relation.startpage	14.6.1	-
dc.relation.lastpage	14.6.18	-
dc.relation.journaltitle	Current Protocols in Nucleic Acid Chemistry	-
dc.identifier.doi	10.1002/0471142700.nc1406s34	-
dc.identifier.scopusid	2-s2.0-58849160400	-
dc.author.google	Jeong L.S.	-
dc.author.google	Tosh D.K.	-
dc.author.google	Choi W.J.	-
dc.author.google	Pal S.	-
dc.contributor.scopusid	정낙신(16028528200)	-
dc.contributor.scopusid	최원준(55732412300;57211762651)	-
dc.date.modifydate	20230627112239	-