2-Phenyl-N-tosylazetidine as a formal 1,4dipole precursor

Ioana Ungureanu; Philippe Klotz; Angèle Schoenfelder; André Mann

doi:10.1039/B101168P

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2-Phenyl-N-tosylazetidine as a formal 1,4 dipole precursorThis paper is dedicated to Professor Camille-Georges Wermuth.Electronic supplementary information (ESI) available: experimental details and characterization for key intermediates, including the ORTEP figures of the X-ray structures for compounds 4a and 10. See http:// www.rsc.org/suppdata/cc/b1/b101168p/

Ioana Ungureanu,^a Philippe Klotz,^a Angèle Schoenfelder^a and André Mann*^a

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* Corresponding authors

^a Laboratoire de Pharmacochimie de la Communication Cellulaire, UMR 7081, Faculté de Pharmacie, 74 route du Rhin, BP 24, Illkirch, France.
E-mail: Andre.mann@pharma.u-strasbg.fr;
Fax: +3(0)3 90 24 43 10;
Tel: +33 (0)3 90 24 42 27

Abstract

N-Tosyl-2-phenylazetidine 1 in the presence of BF₃·Et₂O reacts as a formal 1,4 dipole with various activated or non activated alkenes.

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Article information

DOI: https://doi.org/10.1039/B101168P
Article type: Communication
Submitted: 05 Feb 2001
Accepted: 07 Mar 2001
First published: 09 May 2001

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Chem. Commun., 2001, 958-959

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2-Phenyl-N-tosylazetidine as a formal 1,4 dipole precursor

I. Ungureanu, P. Klotz, A. Schoenfelder and A. Mann, Chem. Commun., 2001, 958 DOI: 10.1039/B101168P

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