IPy 2 BF 4 -Mediated Glycosylation and Glycosyl Fluoride Formation
A facile method to convert thioglycosides to glycosyl fluorides with Ipy2BF4 (py = pyridine) is presented. Alternatively, activation of thioglycosides with Ipy2BF4 in the presence of acids and glycosyl acceptors led to glycosylation reactions. Perbenzylated (armed) glycosyl donors yielded predominan...
Published in: | European Journal of Organic Chemistry |
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Main Authors: | , |
Format: | Article in Journal/Newspaper |
Language: | English |
Published: |
2007
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Subjects: | |
Online Access: | https://archive-ouverte.unige.ch/unige:24446 |
Summary: | A facile method to convert thioglycosides to glycosyl fluorides with Ipy2BF4 (py = pyridine) is presented. Alternatively, activation of thioglycosides with Ipy2BF4 in the presence of acids and glycosyl acceptors led to glycosylation reactions. Perbenzylated (armed) glycosyl donors yielded predominantly the β-anomeric product. This methodology is compatible with one-pot sequential glycosylation. |
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