Issue 22, 2002

1,3-Dipolar cycloaddition reactions of carbohydrate derived nitrones and oximes

Abstract

Covering: 1990–June 2002

This review aims to summarise key features of the synthesis and 1,3-dipolar cycloaddition reactions of carbohydrate derived nitrones and oximes, allowing access to isoxazolines and isoxazolidines. An alternative approach to these targets, which involves the reaction of non-carbohydrate dipoles with carbohydrate derived alkenes, is also described.

Graphical abstract: 1,3-Dipolar cycloaddition reactions of carbohydrate derived nitrones and oximes

Article information

Article type
Review Article
Submitted
06 Aug 2002
First published
17 Oct 2002

J. Chem. Soc., Perkin Trans. 1, 2002, 2419-2438

1,3-Dipolar cycloaddition reactions of carbohydrate derived nitrones and oximes

H. M.I. Osborn, N. Gemmell and L. M. Harwood, J. Chem. Soc., Perkin Trans. 1, 2002, 2419 DOI: 10.1039/B200549M

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