REGIOSELECTIVE AND STEREOSELECTIVE SYNTHESIS OF 3,6-DIEN-1-YNES BY NICKEL-CATALYZED COUPLING REACTION OF ALLYL CHLORIDES, 1-ALKYNES, AND ALKYNYLTINS

Authors
IKEDA S CUI DM SATO Y
Citation
S. Ikeda et al., REGIOSELECTIVE AND STEREOSELECTIVE SYNTHESIS OF 3,6-DIEN-1-YNES BY NICKEL-CATALYZED COUPLING REACTION OF ALLYL CHLORIDES, 1-ALKYNES, AND ALKYNYLTINS, Journal of organic chemistry, 59(23), 1994, pp. 6877-6878
Citations number
17
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Journal of organic chemistry → ACNP
ISSN journal
00223263
Volume
59
Issue
23
Year of publication
1994
Pages
6877 - 6878
Database
ISI
SICI code
0022-3263(1994)59:23<6877:RASSO3>2.0.ZU;2-G
Abstract
In the presence of a nickel catalyst prepared from Ni(acac)(2) and DIB ALH (1/1) in situ, three-component coupling reaction of allyl chloride s, 1-alkynes, and alkynyltins yielded regio- and stereoselective 3,6-d ien-1-ynes in THF.