Issue 6, 2000

1,3-Dipolar cycloaddition of 2-azetidinone-tethered azomethine ylides. Application to the rapid, stereocontrolled synthesis of optically pure highly functionalised pyrrolizidine systems

Abstract

A new straightforward methodology to prepare polyfunctionalised enantiopure pyrrolizidine systems, based on the 1,3-dipolar cycloaddition of 2-azetidinone-tethered azomethine ylides as the key reaction, is presented.

Article information

Article type
Communication
Submitted
04 Jan 2000
Accepted
14 Feb 2000
First published
07 Mar 2000

Chem. Commun., 2000, 485-486

1,3-Dipolar cycloaddition of 2-azetidinone-tethered azomethine ylides. Application to the rapid, stereocontrolled synthesis of optically pure highly functionalised pyrrolizidine systems

B. Alcaide, P. Almendros, J. M. Alonso and M. F. Aly, Chem. Commun., 2000, 485 DOI: 10.1039/B000249F

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