Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/6227
Full metadata record
DC FieldValueLanguage
dc.contributor.authorJoshi, Vishal Y-
dc.contributor.authorSawant, Manohar R-
dc.date.accessioned2009-10-21T04:41:03Z-
dc.date.available2009-10-21T04:41:03Z-
dc.date.issued2006-02-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/6227-
dc.description461-465en_US
dc.description.abstractThe Koenigs-Knorr method plays a prominent role in the stereoselective synthesis of alkyl D-glucopyranosides via glycosidic linkage. Such an approach requires costly and toxic promoter salts of silver or mercury, which have additional separation problems. In a novel method a less toxic promoter salt like LiCO3 is used for glycosidation of several fatty alcohols including an aromatic alcohol. LiCO3 can be easily separated from the reaction mass and gives good yield.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesInt.Cl.7 C 07 H 3/00en_US
dc.sourceIJC-B Vol.45B(02) [February 2006]en_US
dc.subjectKoenigs-Knorr methoden_US
dc.subject-D-glucopyranosidesen_US
dc.subjectalkyl glucosidesen_US
dc.subjectLiCO3en_US
dc.titleA convenient stereoselective synthesis of -D-glucopyranosidesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.45B(02) [February 2006]

Files in This Item:
File Description SizeFormat 
IJCB 45B(2) 461-465.pdf157.21 kBAdobe PDFView/Open


Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.