Issue 6, 2000
From the journal:

Chemical Communications

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

Benito Alcaide,*a   Pedro Almendros,a   Jose M. Alonsoa  and  Moustafa F. Aly†a  

* Corresponding authors

a Departamento de Química Orgánica I, Facultad de Ciencias Químicas, Universidad Complutense, Madrid, Spain.
E-mail: E-mail: alcaideb@eucmax.sim.ucm.es

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.

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Article information

DOI
https://doi.org/10.1039/B000249F
Article type
Communication
Submitted
04 Jan 2000
Accepted
14 Feb 2000
First published
07 Mar 2000

Chem. Commun., 2000, 485-486

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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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