Intramolecular homolytic displacement of cobaloxime (II) from saturated carbon. A novel synthesis of (trichloroethyl) cyclopentanes and sulfolanes

P Bougeard, A Bury, CJ Cooksey…

Index: Bougeard,P.; Bury,A.; Cooksey,C.J. Journal of the American Chemical Society, 1982 , vol. 104, p. 5230

Full Text: HTML

Citation Number: 8

Abstract

12 a M= Co (dmgH), py. hex-5-enyl radical (branch b) I0 and abstraction of a chlorine atom from 2 by the cyclopentylmethyl radical. When the same reaction is carried out in the presence of a large excess of 2 or of trichloromethanesulfonyl chloride (4), not only does the rate at which the hex-5-enyl radical abstracts a chlorine atom from 2 or from 4 (Scheme I, branch c) become larger than the rate at which that radical rearranges but the radical ...

Related Articles:

Homolytic displacement at saturated carbon. Part 9. The reactions of trichloromethanesulfonyl chloride with pent-4-enylcobaloximes and with olefins. A novel route to ( …

[Ashcroft, Martyn M.; Bougeard, Peter; Bury, Adrian; Cooksey, Christopher J.; Johnson, Michael D.; et al. Journal of Organic Chemistry, 1984 , vol. 49, # 10 p. 1751 - 1761]

More Articles...