Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/22498
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dc.contributor.authorShu-Jia, Zhang-
dc.contributor.authorQun, Liu-
dc.contributor.authorYao-zu, Chen-
dc.date.accessioned2013-10-23T04:33:13Z-
dc.date.available2013-10-23T04:33:13Z-
dc.date.issued2000-02-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/22498-
dc.description147-150en_US
dc.description.abstractActive methylene compounds 3 react with CS2, 2-bromoethanol in the presence of K2CO3 to give two products 4 and 5 through one-pot reaction. Acylketene cyclic O,S-ethylene acetals 10 have been synthesized by the displacement of 2 with 2-mercaptoethanoi using sodium tert-butoxide as base. Configurations of the compounds 4 and 10 have been confirmed by X-ray results and 1H NMR data. The mechanism has been discussed.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-B Vol.39B(02) [February 2000]en_US
dc.titleStudies on the one-pot reaction of active methylene compounds with 2-bromoethanol—Preparation of α-oxoketene cyclic O,S-ethylene acetalsen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.39B(02) [February 2000]

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