Photolysis of 2-dialkylamino-3-methyl-1,4-naphthoquinones |
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Authors: | A. D. Bukhtoyarova V. N. Berezhnaya R. P. Shishkina V. P. Vetchinov V. I. Eroshkin T. A. Stavitskaya |
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Affiliation: | (1) Novosibirsk Institute of Organic Chemistry, Siberian Branch, Academy of Sciences of the USSR, USSR |
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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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