Addition Radicalaire du Propanal à Divers Alcènes et Cyclènes: Aspects Stériques et Polaires

I Tabbaa, M Cazaux, R Lalande

Index: Tabbaa, I.; Cazaux, M.; Lalande, R. Bulletin des Societes Chimiques Belges, 1983 , vol. 92, # 11-12 p. 1011 - 1018

Full Text: HTML

Citation Number: 2

Abstract

Abstract Free radical addition of propanal to double bonds, initiated by benzoyl peroxide, mainly leads to two adducts, an aldehyde and a ketone, when the double bond has a methylene group; these results are explained in terms of polar effects in the free radical transfert reactions. When the double bond has no methylene group, only the ketonic adduct is obtained; the steric effects in the free radical addition step explain these results.

Related Articles:

Novel acylation of aliphatic olefins promoted by active zinc compounds

[Shono, Tatsuya; Nishiguchi, Ikuzo; Sasaki, Manji; Ikeda, Haruhiko; Kurita, Makoto Journal of Organic Chemistry, 1983 , vol. 48, # 15 p. 2503 - 2505]

More Articles...