Abstract
Mechanisms of transglycosylation reactions in the nucleoside chemistry and their modern interpretations are presented. Special attention is paid to the formation of kinetically controlled and thermodynamic products, reaction intermediates, correlation of tautomerism and regioselectivity in glycosyl migration reactions, their stereoselectivity and reversibility as well as side-reactions like anomerization or cyclization. Some synthetic applications of transglycosylation are also discussed.
Current Organic Chemistry
Title: Reactions of Transglycosylation in the Nucleoside Chemistry
Volume: 12 Issue: 4
Author(s): Jerzy Boryski
Affiliation:
Abstract: Mechanisms of transglycosylation reactions in the nucleoside chemistry and their modern interpretations are presented. Special attention is paid to the formation of kinetically controlled and thermodynamic products, reaction intermediates, correlation of tautomerism and regioselectivity in glycosyl migration reactions, their stereoselectivity and reversibility as well as side-reactions like anomerization or cyclization. Some synthetic applications of transglycosylation are also discussed.
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Cite this article as:
Boryski Jerzy, Reactions of Transglycosylation in the Nucleoside Chemistry, Current Organic Chemistry 2008; 12 (4) . https://dx.doi.org/10.2174/138527208783743723
DOI https://dx.doi.org/10.2174/138527208783743723 |
Print ISSN 1385-2728 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5348 |
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