Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/44091
Title: Homolytic displacement at saturated carbon: Part 7-Synthesis of cyclic, bicyclic and spirocyclic sulphones from the corresponding butenyl cobaloximes with thiophene- 2-sulphonyl chloride
Authors: Gupta, B D
Das, Indira
Dixit, Vandana
Issue Date: Dec-1993
Publisher: NISCAIR-CSIR, India
Abstract: The reactions of but-3-enyl cobaloximes with thiophene-2-sulphonyl chloride under thermal and photochemical conditions give the corresponding cyclopropylmethyl sulphones. A similar reaction with cyclopent-2-enylmethyl and cyclohex-2-enylmethyl cobaloximes gives a mixture of cis- and trans- bicyclic products. Cycloalkane, spirocycloprop-2-yl sulphone is formed exclusively from the reaction of 2-(cycloalk-1-enyl)ethyl cobaloxime. The reactions are interpreted in terms of SH 2 mechanism.
Page(s): 1019-1022
URI: http://nopr.niscair.res.in/handle/123456789/44091
ISSN: 0975-0975(Online); 0376-4710(Print)
Appears in Collections:IJC-A Vol.32A(12) [December 1993]

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