Applications of the Baylis-Hillman reaction 2: A simple stereoselective synthesis of (E)- and (Z)-trisubstituted alkenes

dc.contributor.author Basavaiah, Deevi
dc.contributor.author Sarma, Pakala K.S.
dc.contributor.author Bhavani, Anagani K.D.
dc.date.accessioned 2022-03-27T09:04:37Z
dc.date.available 2022-03-27T09:04:37Z
dc.date.issued 1994-12-01
dc.description.abstract Reaction of Grignard reagents with methyl 3-acetoxy-2-methylenealkanoates produces (2E)-2-substituted alk-2-enoates, whereas a similar reaction with 3-acetoxy-2-methylenealkanenitriles provides (2Z)-2-substituted alk-2-enenitriles in high (Z)-stereoselectivity.
dc.identifier.citation Journal of the Chemical Society, Chemical Communications
dc.identifier.issn 00224936
dc.identifier.uri 10.1039/C39940001091
dc.identifier.uri http://xlink.rsc.org/?DOI=C39940001091
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12375
dc.title Applications of the Baylis-Hillman reaction 2: A simple stereoselective synthesis of (E)- and (Z)-trisubstituted alkenes
dc.type Journal. Article
dspace.entity.type
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