Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/18786
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dc.contributor.authorBettadaiah, B K-
dc.contributor.authorSrinivas, P-
dc.date.accessioned2013-06-07T07:20:22Z-
dc.date.available2013-06-07T07:20:22Z-
dc.date.issued2004-06-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/18786-
dc.description1339-1340en_US
dc.description.abstractTri-substituted terpene and aryl-substituted epoxides react with bromine and dimethyl sulfide to afford α-bromoketones or α-bromoaldehydes as the major products in good yields. The reaction is regio-specific and occurs smoothly in the presence of aromatic and hydroxyl groups in the substrates.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.relation.ispartofseriesInt.Cl.7 C 07 C 13/18en_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.43B(06) [June 2004]en_US
dc.titleRegio-specific ring opening of terpene and aryl-substituted epoxides with Br2/DMS reagenten_US
dc.typeArticleen_US
Appears in Collections: IJC-B Vol.43B(06) [June 2004]

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