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	2016-11-26T02:11:36Z	-
dc.date.available	2016-11-26T02:11:36Z	-
dc.date.issued	2008	-
dc.identifier.issn	1934-9289	-
dc.identifier.other	OAK-17992	-
dc.identifier.uri	https://dspace.ewha.ac.kr/handle/2015.oak/232851	-
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.	-
dc.language	English	-
dc.title	Synthesis of fluoroneplanocin A.	-
dc.type	Article	-
dc.relation.volume	Chapter 14	-
dc.relation.index	SCOPUS	-
dc.relation.journaltitle	Current protocols in nucleic acid chemistry / edited by Serge L. Beaucage ... [et al.]	-
dc.identifier.scopusid	2-s2.0-55949083780	-
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	-