A formal synthesis of (+)-(S)-kurasoin B

dc.contributor.author	Yuste, F
dc.contributor.author	Mastranzo, VM
dc.contributor.author	Ortiz, B
dc.contributor.author	Ruano, JLG
dc.contributor.author	Sánchez-Obregon, R
dc.date.accessioned	2011-01-22T10:25:52Z
dc.date.available	2011-01-22T10:25:52Z
dc.date.issued	2009
dc.identifier.issn	1424-6376
dc.identifier.uri	http://hdl.handle.net/11154/912
dc.description.abstract	A new diastereoselective synthesis of (S)-1-[(S)-oxiran-2-yl]-2-phenylethanone (10), a key intermediate in the synthesis of kurasoin B (2), has been accomplished in seven steps in an overall yield of 32%. The key synthetic step in the process is the diastereoselective reduction of the beta-keto sulfoxide 6 derived from (S)-phenyllactic acid.	en_US
dc.language.iso	en	en_US
dc.title	A formal synthesis of (+)-(S)-kurasoin B	en_US
dc.type	Article	en_US
dc.identifier.idprometeo	532
dc.source.novolpages	:211-217
dc.subject.wos	Chemistry, Organic
dc.description.index	WoS: SCI, SSCI o AHCI
dc.subject.keywords	Kurasoin B
dc.subject.keywords	diastereoselective synthesis
dc.subject.keywords	beta-keto sulfoxides
dc.subject.keywords	DIBAH/ZnBr2 reduction
dc.relation.journal	Arkivoc