Versatile Spirocyclic Glycine‐Based Nitrones and Their Highly Stereoselective 1,3‐Dipolar Cycloaddition: Synthetic Communications: Vol 37, No 2

Synthetic Communications

An International Journal for Rapid Communication of Synthetic Organic Chemistry

Volume 37, 2007 - Issue 2

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Abstract

A convenient and efficient method for the synthesis of novel spirocyclic nitrones prepared from glycine derivatives is reported. The 1,3‐cycloaddition reactions of the nitrones with alkenes lead to novel isoxazolidines in high yields and with excellent regio‐ and stereoselectivity.

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Versatile Spirocyclic Glycine‐Based Nitrones and Their Highly Stereoselective 1,3‐Dipolar Cycloaddition

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Versatile Spirocyclic Glycine‐Based Nitrones and Their Highly Stereoselective 1,3‐Dipolar Cycloaddition

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