Bulletin of the Academy of Sciences of the USSR Division of Chemical Science p. 2094 - 2098 (1991)
Update date:2022-08-29
Topics:
Bukhtoyarova, A. D.
Berezhnaya, V. N.
Shishina, R. P.
Vetchinov, V. P.
Eroshkin, V. I.
Stavitskaya, T. A.
The photolysis of 2-dialkylamino-1,4-naphthoquinones is significantly more efficient when a methyl group is at C3.The quantum yields are 2-6 times greater than for 2-dialkylaminonaphthoquinones lacking a methyl group. 2-Monoalkylamino-1,4-naphthoquuinones also undergo photochemical dealkylation.
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