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

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

Martine Maillard-Boyeremail, Caroline Castera-Ducrosemail, Pierre Verhaegheemail, France Sifrediemail, Pascal Rathelotemail and Patrice Vanelle* email
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
* Author to whom correspondence should be addressed.
Received: 26 January 2010; in revised form: 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

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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.

AMA 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(4):2719-2729.

Chicago/Turabian Style

Maillard-Boyer, Martine; Castera-Ducros, Caroline; Verhaeghe, Pierre; Sifredi, France; Rathelot, Pascal; Vanelle, Patrice. 2010. "Access to Original Vinylic Chlorides in the Quinazoline Series via a Monoelectronic Transfer Reaction Approach." Molecules 15, no. 4: 2719-2729.

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