Publication Type:

Journal Article

Source:

Indian Journal of Chemistry, NISCAIR-CSIR, Volume 40, India, p.986–988 (2001)

URL:

http://nopr.niscair.res.in/handle/123456789/18564

Abstract:

The reactions of MeC6H4-SO2-SPh with organocobaloximes, RCo(dmgH)2Py, (R= alkyl, benzyl, butenyl and allyl) under visible light photolysis show that the alkyl, butenyl and benzyl cobaloximes form the corresponding sulphides whereas the allyl cobaloximes form the organic sulphones.

Cite this Research Publication

Dr. Yamuna R., V. Kanth, V., Singh, V., Gupta, B. D., Oberoi, M., and Mandal, D., “Homolytic displacements at carbon in organocobaloximes: Reactions of organocobaloximes with free radical precursor with two radical centres”, Indian Journal of Chemistry, vol. 40, pp. 986–988, 2001.

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