The Johnson-Claisen rearrangement of 3-hydroxy-2-methylenealkanenitriles: Stereoselective synthesis of functionalized trisubstituted alkenes

dc.contributor.author Basavaiah, Deevi
dc.contributor.author Pandiaraju, Subramanian
dc.date.accessioned 2022-03-27T09:04:30Z
dc.date.available 2022-03-27T09:04:30Z
dc.date.issued 1995-01-30
dc.description.abstract A simple stereoselective synthesis of ethyl (4Z)-4-cyanoalk-4-enoates via the Johnson-Claisen rearrangement of 3-hydroxy-2-methylenealkanenitriles is described. © 1995.
dc.identifier.citation Tetrahedron Letters. v.36(5)
dc.identifier.issn 00404039
dc.identifier.uri 10.1016/0040-4039(94)02360-N
dc.identifier.uri https://www.sciencedirect.com/science/article/abs/pii/004040399402360N
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12372
dc.title The Johnson-Claisen rearrangement of 3-hydroxy-2-methylenealkanenitriles: Stereoselective synthesis of functionalized trisubstituted alkenes
dc.type Journal. Article
dspace.entity.type
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