A facile regioselective 1,6-O-diacetylation method of methyl- glycopyranosides and their dimethyl phosphonates

Article abstract of DOI:10.1080/00397919708006792

A general method of 1,6-di-O-acetylation of methyl-α/β- glycopyranosides and a strategy to synthesize protected dimethyl (2,3,4-tri- O-benzyl-α-D-glycosyl) phosphonate having a free OH at C-6 are reported.

Full text of DOI:10.1080/00397919708006792

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Synthetic Communications: An
International Journal for Rapid
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Organic Chemistry
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A Facile Regioselective 1,6-
O-Diacetylation Method of
Methyl-Glycopyranosides and
Their Dimethyl Phosphonates
Guang-tao Zhang a b , Zhong-wu Guo a & Yong-zheng
Hui a
a National Laboratory of Bio-organic and Natural
Products Chemistry , Shanghai Institute of Organic
Chemistry, Chinese Academy of Sciences , Shanghai,
200032, China
b Department of Chemical Physics , the University
of Science and Technology of China , Hefei, 230026,
China
Published online: 22 Aug 2006.
To cite this article: Guang-tao Zhang , Zhong-wu Guo & Yong-zheng Hui (1997) A
Facile Regioselective 1,6-O-Diacetylation Method of Methyl-Glycopyranosides and
Their Dimethyl Phosphonates, Synthetic Communications: An International Journal
for Rapid Communication of Synthetic Organic Chemistry, 27:11, 1907-1917, DOI:
10.1080/00397919708006792
To link to this article: http://dx.doi.org/10.1080/00397919708006792
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