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Photolysis of 2-dialkylamino-3-methyl-1,4-naphthoquinones
Authors:A D Bukhtoyarova  V N Berezhnaya  R P Shishkina  V P Vetchinov  V I Eroshkin  T A Stavitskaya
Institution:(1) Novosibirsk Institute of Organic Chemistry, Siberian Branch, Academy of Sciences of the USSR, USSR
Abstract: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-Monoalkyl-amino-1,4-naphthoquinones also undergo photochemical dealkylation.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 10, pp. 2387–2392, October, 1991.
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