Issue 12, 2004

Rearrangement of pyrrolines derived from the Birch reduction of electron-deficient pyrroles: radical ring-expansion to substituted tetrahydropyridines

Abstract

Access to the synthetically important tetrahydropyridine motif has been achieved by radical rearrangement of pyrrolines obtained from the Birch reduction of electron-deficient pyrroles.

Graphical abstract: Rearrangement of pyrrolines derived from the Birch reduction of electron-deficient pyrroles: radical ring-expansion to substituted tetrahydropyridines

Article information

Article type
Communication
Submitted
16 Mar 2004
Accepted
20 Apr 2004
First published
18 May 2004

Chem. Commun., 2004, 1422-1423

Rearrangement of pyrrolines derived from the Birch reduction of electron-deficient pyrroles: radical ring-expansion to substituted tetrahydropyridines

P. G. Turner, T. J. Donohoe and R. P. C. Cousins, Chem. Commun., 2004, 1422 DOI: 10.1039/B404002C

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