Article ID Journal Published Year Pages File Type
5221546 Tetrahedron 2011 9 Pages PDF
Abstract

Pyranosides with 2,3-trans carbamate or 2,3-trans carbonate groups are anomerized under mild acidic conditions via endocyclic cleavage reaction. In order to understand the nature of the anomerization reaction via the endocyclic cleavage-recyclization process, the substituent effects at various positions were investigated.

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Physical Sciences and Engineering Chemistry Organic Chemistry
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Substituent effects in endocyclic cleavage-recyclization anomerization reaction of pyranosides
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