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

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Received: 26 January 2010; in revised form: 21 February 2010 / Accepted: 12 April 2010 / Published: 13 April 2010
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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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