A new strategy for the stereoselective syntheses of C-glycosyl compounds of β-pentapyranoses

Article abstract of DOI:10.1080/00397919608003565

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.

Full text of DOI:10.1080/00397919608003565

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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A New Strategy for the
Stereoselecitve Syntheses of
C-Glycosyl Compounds of β-
Pentapyranoses
Zhong-Wu Guo a & Yong-Zheng Hui a
a National Laboratory of Bio-organic and Natural
Product Chemistry Shanghai Institute of Organic
Chemistry, Chinese Academy of Sciences , Shanghai,
200032, China
Published online: 21 Aug 2006.
To cite this article: Zhong-Wu Guo & Yong-Zheng Hui (1996) A New Strategy for the
Stereoselecitve Syntheses of C-Glycosyl Compounds of β-Pentapyranoses, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 26:11, 2067-2073, DOI: 10.1080/00397919608003565
To link to this article: http://dx.doi.org/10.1080/00397919608003565
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