Issue 14, 2006
From the journal:

Organic & Biomolecular Chemistry

Preparation of highly substituted pyrrolidinesvia an organometallic dipole†

Steven D. R. Christie,*a   Ryan J. Davoilea  and  Raymond C. F. Jones*a  

* Corresponding authors

a Chemistry Department, Loughborough University, Loughborough, Leics, UK
E-mail: S.D.Christie@lboro.ac.uk, R.C.F.Jones@lboro.ac.uk
Fax: +44 1509 223926
Tel: +44 1509 222587 (S. D. R. Christie)

Abstract

Highly substituted pyrrolidines are prepared by formal cycloaddition of imines to a metal-stabilised ‘Nicholas’ dipole derived from an alkyne–cyclopropane dicobalt complex.

Graphical abstract: Preparation of highly substituted pyrrolidines via an organometallic dipole

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Article information

DOI
https://doi.org/10.1039/B605329G
Article type
Communication
Submitted
13 Apr 2006
Accepted
01 Jun 2006
First published
14 Jun 2006

Org. Biomol. Chem., 2006,4, 2683-2684

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Preparation of highly substituted pyrrolidines via an organometallic dipole

S. D. R. Christie, R. J. Davoile and R. C. F. Jones, Org. Biomol. Chem., 2006, 4, 2683 DOI: 10.1039/B605329G

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