Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5223358 | Tetrahedron | 2009 | 7 Pages |
Abstract
The photoreaction of dicyanobenzenes with aliphatic carboxylate ions afforded alkylcyanobenzenes and alkyldicyanobenzenes via decarboxylative substitution. The redox-photosensitized reaction system was effective in improving the product yield. The efficiency of this photoreaction depended on the structure of the carboxylate ion, and the product distribution varied with the dicyanobenzenes employed. This photoreaction was proved to be a clean process for the preparation of alkylcyanobenzenes.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Tatsuya Itou, Yasuharu Yoshimi, Toshio Morita, Yuji Tokunaga, Minoru Hatanaka,