MICHAEL REACTIONS OF SILYLATED NUCLEOPHILES WITH CONJUGATED ENONES ACCOMPANIED BY SILYL GROUP-TRANSFER CATALYZED BY COPPER(I) CHLORIDE UNDER PHOTOIRRADIATION

Authors
MITANI M OSAKABE Y
Citation
M. Mitani et Y. Osakabe, MICHAEL REACTIONS OF SILYLATED NUCLEOPHILES WITH CONJUGATED ENONES ACCOMPANIED BY SILYL GROUP-TRANSFER CATALYZED BY COPPER(I) CHLORIDE UNDER PHOTOIRRADIATION, Journal of the Chemical Society, Chemical Communications, (15), 1994, pp. 1759-1760
Citations number
11
Categorie Soggetti
Chemistry
Journal title
Journal of the Chemical Society, Chemical Communications → ACNP
ISSN journal
00224936
Issue
15
Year of publication
1994
Pages
1759 - 1760
Database
ISI
SICI code
0022-4936(1994):15<1759:MROSNW>2.0.ZU;2-Y
Abstract
Photoreaction of conjugated enones with silylated nucleophiles such as silyl acetals, silyl enol ethers and even an allyl silane resulted in the formation of Michael adducts accompanied by transfer of the silyl group.