
Journal of Organic Chemistry p. 1837 - 1838 (1984)
Update date:2022-07-29
Topics:
Sakamoto, Masami
Aoyama, Hiromu
Omote, Yoshimori
Photolysis of N-acylthiobenzamides in benzene gave thioketones via a novel photorearrangement involving 1,2-thiobenzoyl shift; the formation of the products was explainable in terms of β-hydrogen abstraction by the thiocarbonyl group.
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