A convenient method for highly selective deprotection of benzylidene acetals from sugars

Article abstract of DOI:10.1080/00397919608003691

A new procedure for cleavage of benzylidene acetals from glycopyranosides using tin (II) chloroide is described which does not affect other protecting groups such as benzoyl, acetyl, benzyl, and acetonide.

Full text of DOI:10.1080/00397919608003691

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Synthetic Communications:
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Synthetic Organic Chemistry
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A Convenient Method
for Highly Selective
Deprotection of Benzylidene
Acetals from Sugars
Jie Xia a & Yongzheng Hui a
a State Key Laboratory of Bio-organic and
Natural Products Chemistry , Shanghai Institute
of Organic Chemistry, Chinese Academy of
Science Shanghai , 200032, China
Published online: 21 Aug 2006.
To cite this article: Jie Xia & Yongzheng Hui (1996) A Convenient Method for
Highly Selective Deprotection of Benzylidene Acetals from Sugars, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 26:5, 881-886, DOI: 10.1080/00397919608003691
To link to this article: http://dx.doi.org/10.1080/00397919608003691
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