THE JOHNSON-CLAISEN REARRANGEMENT OF 5-HYDROXY-2-METHYLENEALKANENITRILES - STEREOSELECTIVE SYNTHESIS OF FUNCTIONALIZED TRISUBSTITUTED ALKENES

Authors
BASAVAIAH D PANDIARAJU S
Citation
D. Basavaiah et S. Pandiaraju, THE JOHNSON-CLAISEN REARRANGEMENT OF 5-HYDROXY-2-METHYLENEALKANENITRILES - STEREOSELECTIVE SYNTHESIS OF FUNCTIONALIZED TRISUBSTITUTED ALKENES, Tetrahedron letters, 36(5), 1995, pp. 757-758
Citations number
12
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
36
Issue
5
Year of publication
1995
Pages
757 - 758
Database
ISI
SICI code
0040-4039(1995)36:5<757:TJRO5>2.0.ZU;2-W
Abstract
A simple stereoselective synthesis of ethyl (4Z)-4-cyanoalk-4-enoates via the Johnson-Claisen rearrangement of 3-hydroxy-2-methylenealkaneni triles is described.