ALKALI-METAL HYDRIDE OR AQUEOUS HYDROXIDE INDUCED CONJUGATE ADDITION OF TRIMETHYLSILYL ENOL ETHERS TO ENONES - A CONVENIENT ALTERNATIVE TO LEWIS-ACID MEDIATED REACTION

Authors
SWAMY VM SARKAR A
Citation
Vm. Swamy et A. Sarkar, ALKALI-METAL HYDRIDE OR AQUEOUS HYDROXIDE INDUCED CONJUGATE ADDITION OF TRIMETHYLSILYL ENOL ETHERS TO ENONES - A CONVENIENT ALTERNATIVE TO LEWIS-ACID MEDIATED REACTION, Tetrahedron letters, 39(10), 1998, pp. 1261-1264
Citations number
21
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
39
Issue
10
Year of publication
1998
Pages
1261 - 1264
Database
ISI
SICI code
0040-4039(1998)39:10<1261:AHOAHI>2.0.ZU;2-Z
Abstract
Conjugate addition to enones by enolates derived from base-induced cle avage of O-Si bond of trimethylsilyl enol ethers, yields 1,5-dicarbony l compounds in good yields. (C) 1998 Elsevier Science Ltd. All rights reserved.