Photochemical Reactions of Acyclic Monothioimides. A Novel Photorearrangement Involving 1,2-Thiobenzoyl Shift
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.
Sakamoto, Masami,Aoyama, Hiromu,Omote, Yoshimori
p. 1837 - 1838
(2007/10/02)
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