Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/21545
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dc.contributor.authorGhosh, Rina-
dc.contributor.authorChakraborty, Arijit-
dc.contributor.authorMaiti, Dilip Kumar-
dc.date.accessioned2013-10-04T11:52:51Z-
dc.date.available2013-10-04T11:52:51Z-
dc.date.issued2003-03-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/21545-
dc.description602-604en_US
dc.description.abstractIn Cl3.3H2O catalysed highly stereoselective O-glycosidation of per-O-acetylglycopyranosyl trichloroacetimidates with a variety of aliphatic alcohols in dichloromethane at room temperature furnishes the corresponding glycosides in very good yields with excellent 1,2-trans stereoselectivity.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.42B(03) [March 2003]en_US
dc.titleIn Cl3.3H2O: An efficient Lewis acid catalyst for stereoselective O-glycosidation reactions of per-O-acetylglycopyranosyl trichloroacetimidatesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.42B(03) [March 2003]

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