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|Title:||A convenient stereoselective synthesis of <img src='/image/spc_char/beta.gif'>-D-glucopyranosides|
|Authors:||Joshi, Vishal Y|
Sawant, Manohar R
|Series/Report no.:||<b>Int</b>.<b>Cl</b>.<b><sup>7</sup> C 07 H 3/00</b>|
|Abstract:||The Koenigs-Knorr method plays a prominent role in the stereoselective synthesis of alkyl D-glucopyranosides <i style="">via</i> 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 LiCO<sub>3 </sub>is used for glycosidation of several fatty alcohols including an aromatic alcohol. LiCO<sub>3</sub> can be easily separated from the reaction mass and gives good yield.|
|Appears in Collections:||IJC-B Vol.45B(02) [February 2006]|
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