Issue 17, 2001
From the journal:

Chemical Communications

Tandem anionic Michael addition/radical cyclizations: a new and efficient strategy for the synthesis of functionalized cyclopentanesElectronic supplementary information (ESI) available: further experimental and spectral data. See http://www.rsc.org/suppdata/cc/b1/b104415j/

Ullrich Jahna  

a Institut für Organische Chemie, TU Braunschweig, Hagenring 30, Braunschweig, Germany
E-mail: u.jahn@tu-bs.de
Fax: 49-531-391-5388
Tel: 49-531-391-7371

Abstract

The combination of anionic Michael addition of lithium ester enolates with radical 5-exo cyclizations through SET oxidation gives highly functionalized cyclopentanes.

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Article information

DOI
https://doi.org/10.1039/B104415J
Article type
Communication
Submitted
18 May 2001
Accepted
02 Jul 2001
First published
01 Aug 2001

Chem. Commun., 2001, 1600-1601

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Tandem anionic Michael addition/radical cyclizations: a new and efficient strategy for the synthesis of functionalized cyclopentanes

U. Jahn, Chem. Commun., 2001, 1600 DOI: 10.1039/B104415J

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