Oxygen-induced reactions of organoboranes with the inert. alpha.,. beta.-unsaturated carbonyl derivatives. Convenient new aldehyde and ketone synthesis via …

HC Brown, GW Kabalka

Index: Brown,H.C.; Kabalka,G.W. Journal of the American Chemical Society, 1970 , vol. 92, # 3 p. 714 - 716

Full Text: HTML

Citation Number: 77

Abstract

71 4 This difficulty was overcome by using a more reactive diacyl peroxide, diacetyl peroxide, at 25”. Under these conditions the catalyzed hydrolysis of the organoborane became much less important, and yields of the 1,4- addition compounds as high as 90%, based on the organoborane, were realized. The following procedure is representative of these studies of the peroxide-catalyzed reaction. A 25-ml flask, fitted with an inlet carrying a rubber septum ...

Related Articles:

Acyl peroxide and photochemical induced reactions of organoboranes with the inert. alpha.,. beta.-unsaturated carbonyl derivatives

[Brown,H.C.; Kabalka,G.W. Journal of the American Chemical Society, 1970 , vol. 92, p. 712 - 714]

Structure and Reactivity. I. The Oximation Rates of Some Straight-Chain and Monomethyl-Substituted Alkanones

[Kletzke,P.G. Journal of Organic Chemistry, 1964 , vol. 29, p. 1363 - 1366]

More Articles...