Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/15495
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dc.contributor.authorGupta, B D-
dc.contributor.authorKanth, V Vijai-
dc.contributor.authorDas, I-
dc.date.accessioned2012-12-31T20:30:42Z-
dc.date.available2012-12-31T20:30:42Z-
dc.date.issued2000-08-
dc.identifier.urihttp://hdl.handle.net/123456789/15495-
dc.description835-837en_US
dc.description.abstractThe reactions of hex-5 -enyl-, 2-allyloxyethyl- and 5-phenylpent-4-ynyl- cobaloximes with arene sulphonyl chlorides under visible light photolysis at O°C give the corresponding cyclized products.  The results are interpreted in terms of SH2' mechanism.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.39A(08) [August 2000]en_US
dc.titleHomolytic bimolecular displacement at carbon in organocobaloximes: Intramolecular cyclizationsen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.39A(08) [August 2000]

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