Facile One-Pot Regioselective Synthesis of 2,3-Mannoepoxy-β-Cyclodextrin

Zhizhong      Wang; Runhua      Lu

doi:10.2174/157017809790442952

Abstract

A simple method for the straightforward regioselective synthesis of 2,3-mannoepoxy-β-cyclodextrin, which is a valuable precursor for further functionalization of β-cyclodextrin, is achieved in one pot at a moderate yield.

Keywords: Cyclodextrins, 2,3-mannoepoxy-β-cyclodextrin, regioselective synthesis, sulfonylimidazole, cyclic oligosaccharides, carbonate buffer

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Letters in Organic Chemistry

Title: Facile One-Pot Regioselective Synthesis of 2,3-Mannoepoxy-β-Cyclodextrin

Volume: 6 Issue: 8

Author(s): Zhizhong Wang and Runhua Lu

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Keywords: Cyclodextrins, 2,3-mannoepoxy-β-cyclodextrin, regioselective synthesis, sulfonylimidazole, cyclic oligosaccharides, carbonate buffer

Abstract: A simple method for the straightforward regioselective synthesis of 2,3-mannoepoxy-β-cyclodextrin, which is a valuable precursor for further functionalization of β-cyclodextrin, is achieved in one pot at a moderate yield.

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Wang Zhizhong and Lu Runhua, Facile One-Pot Regioselective Synthesis of 2,3-Mannoepoxy-β-Cyclodextrin, Letters in Organic Chemistry 2009; 6 (8) . https://dx.doi.org/10.2174/157017809790442952