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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 26, 1996 - Issue 11
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Original Articles

A New Strategy for the Stereoselecitve Syntheses of C-Glycosyl Compounds of β-Pentapyranoses

Zhong-Wu Guo National Laboratory of Bio-organic and Natural Product Chemistry Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai, 200032, China
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Yong-Zheng Hui National Laboratory of Bio-organic and Natural Product Chemistry Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai, 200032, China
Pages 2067-2073 | Received 11 Oct 1995, Published online: 21 Aug 2006
 
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Abstract

The C-glycosyl compounds of β-L-xylopyranose and β-D-arabinopyranose were conveniently prepared by reduction of methyl α-D-glucopyranoside and methyl α-D-mannopyranoside with triethylsilane in the presence of trimethylsilyl trifluoromethanesulfonate, respectively.

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