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PHOTOLYSIS OF 2-DIALKYLAMINO-3-METHYL-1,4-NAPHTHOQUINONES Full article

Journal Bulletin of the Academy of Sciences of the USSR Division of Chemical Science
ISSN: 0568-5230
Output data Year: 1991, Volume: 40, Number: 10, Pages: 2094-2098 Pages count : 5 DOI: 10.1007/BF00963513
Authors Bukhtoyarova A.D. 1 , Berezhnaya V.N. 1 , Shishkina R.P. 1 , Vetchinov V.P. 1 , Eroshkin V.I. 1 , Stavitskaya T.A. 1
Affiliations
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.
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 OpenAlex
Dates:
Published print: Oct 1, 1991
Identifiers:
Web of science: WOS:A1991JA48600016
Scopus: 2-s2.0-34249926446
Elibrary: 30896011
OpenAlex: W1993443921
Citing:
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