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Molecules 2010, 15(4), 2719-2729; doi:10.3390/molecules15042719

Access to Original Vinylic Chlorides in the Quinazoline Series via a Monoelectronic Transfer Reaction Approach

Laboratoire de Pharmacochimie Radicalaire, Faculté de Pharmacie, Universités d’Aix-Marseille I, II et III - UMR CNRS 6264, Laboratoire Chimie Provence, 27 Boulevard Jean Moulin, 13385 Marseille cedex 05, France
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Received: 26 January 2010 / Revised: 21 February 2010 / Accepted: 12 April 2010 / Published: 13 April 2010
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Abstract

A series of new quinazoline derivatives bearing a vinylic chloride group on the 2-position was prepared by using a consecutive SRN1 / ERC1 radical strategy.
Keywords: SRN1; ERC1; quinazoline ring; vinylic chlorides SRN1; ERC1; quinazoline ring; vinylic chlorides
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This is an open access article distributed under the Creative Commons Attribution License (CC BY 3.0).

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MDPI and ACS Style

Maillard-Boyer, M.; Castera-Ducros, C.; Verhaeghe, P.; Sifredi, F.; Rathelot, P.; Vanelle, P. Access to Original Vinylic Chlorides in the Quinazoline Series via a Monoelectronic Transfer Reaction Approach. Molecules 2010, 15, 2719-2729.

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