Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
6493140 | Journal of Photochemistry and Photobiology A: Chemistry | 2009 | 5 Pages |
Abstract
Photoreactions of 2-cyano-6-methoxynaphthalene with methoxy-substituted 1,2-diarylcyclopropanes in benzene give 2-cyano-1-(1,3-diarylpropyl)-6-methoxynaphthalenes. The excellent regioselectivity seen in these processes can be explained by initial formation of singlet exciplexes, in which the dipoles of each component are oriented in opposite directions.
Keywords
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Bioengineering
Authors
Hajime Maeda, Shoji Matsuda, Kazuhiko Mizuno,