Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/41549
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dc.contributor.authorGupta, B D-
dc.contributor.authorDas, Indira-
dc.date.accessioned2017-05-01T05:48:31Z-
dc.date.available2017-05-01T05:48:31Z-
dc.date.issued1996-12-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/41549-
dc.description1111-1113en_US
dc.description.abstractSeveral allyl (both cyclic and acyclic), allenyl, hexenyl and propargylcobaloximes react regiospecifically with thiophone-2-sulphonyl chloride under thermal and photochemical conditions to give the corresponding sulphones. The reaction is believed to take place by the attack of the sulphur radical on the terminal carbon of the organocobaloxime with the displacement of cobaloxime(II).en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-A Vol.35A(12) [December 1996]en_US
dc.titleHomolytic displacement at carbon in organocobaloximes: Part 9­-Reactions of organocobaloximes with thiophene 2-sul-phonylchlorideen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.35A(12) [December 1996]

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