A new highly regioselective reaction of unprotected sugars for chemical synthesis of 6-acyl-D-glycopyranosides

Article abstract of DOI:10.1080/00397919508011779

New methodologies developed to synthesize 6-acyl-D-glycopyranosides are described. Thus, regioselective acylation of non protected glycopyranosides was performed using acyl-p-nitrothiophenol esters and acyl-2,4-dinitrophenol esters as the acylating reagen

Full text of DOI:10.1080/00397919508011779

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Synthetic Communications: An
International Journal for Rapid
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Organic Chemistry
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A New Highly Regioselective
Reaction of Unprotected Sugars
for Chemical Synthesis of 6-
Acyl-D-Glycopyranosides
Jie Xia a & Yongzheng Hui a
a State Key Laboratory of Bio-organic and Natural
Products Chemistry, Shanghai Institute of Organic
Chemistry, Chinese Acdemy of Science , Shanghai,
200032, China
Published online: 23 Sep 2006.
To cite this article: Jie Xia & Yongzheng Hui (1995) A New Highly Regioselective
Reaction of Unprotected Sugars for Chemical Synthesis of 6-Acyl-D-Glycopyranosides,
Synthetic Communications: An International Journal for Rapid Communication of
Synthetic Organic Chemistry, 25:15, 2235-2251, DOI: 10.1080/00397919508011779
To link to this article: http://dx.doi.org/10.1080/00397919508011779
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