PHOTOLYSIS OF 2-DIALKYLAMINO-3-METHYL-1,4-NAPHTHOQUINONES Full article
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Bulletin of the Academy of Sciences of the USSR Division of Chemical Science
ISSN: 0568-5230 |
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| Output data | Year: 1991, Volume: 40, Number: 10, Pages: 2094-2098 Pages count : 5 DOI: 10.1007/BF00963513 | ||
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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.
Cite:
Bukhtoyarova A.D.
, Berezhnaya V.N.
, Shishkina R.P.
, Vetchinov V.P.
, Eroshkin V.I.
, Stavitskaya T.A.
PHOTOLYSIS OF 2-DIALKYLAMINO-3-METHYL-1,4-NAPHTHOQUINONES
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 1991. V.40. N10. P.2094-2098. DOI: 10.1007/BF00963513 WOS Scopus РИНЦ
PHOTOLYSIS OF 2-DIALKYLAMINO-3-METHYL-1,4-NAPHTHOQUINONES
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 1991. V.40. N10. P.2094-2098. DOI: 10.1007/BF00963513 WOS Scopus РИНЦ
Dates:
| Published print: | Oct 1, 1991 |
Identifiers:
| Web of science | WOS:A1991JA48600016 |
| Scopus | 2-s2.0-34249926446 |
| Elibrary | 30896011 |
| OpenAlex | W1993443921 |