Abstract
The 3+2 cycloaddition reaction of nitrones and nitrile oxides with activated exo-glycals obtained from the Wittig reaction of sugar lactones gave good yields of only two cycloadducts. The reaction was efficiently carried out under microwave activation.
Keywords: dipolar cycloaddition, exo-glycals, spironucleosides, microwave activation
Letters in Organic Chemistry
Title: Cycloaddition of Nitrones and Nitrile Oxides to Activated Exo-glycals
Volume: 2 Issue: 3
Author(s): C. Taillefumier, G. Enderlin and Y. Chapleur
Affiliation:
Keywords: dipolar cycloaddition, exo-glycals, spironucleosides, microwave activation
Abstract: The 3+2 cycloaddition reaction of nitrones and nitrile oxides with activated exo-glycals obtained from the Wittig reaction of sugar lactones gave good yields of only two cycloadducts. The reaction was efficiently carried out under microwave activation.
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Cite this article as:
Taillefumier C., Enderlin G. and Chapleur Y., Cycloaddition of Nitrones and Nitrile Oxides to Activated Exo-glycals, Letters in Organic Chemistry 2005; 2 (3) . https://dx.doi.org/10.2174/1570178053765339
DOI https://dx.doi.org/10.2174/1570178053765339 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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