PHOTOLYSIS OF 1,2-ANTHRAQUINONE DIAZIDE IN AROMATIC-HYDROCARBONS

PHOTOLYSIS OF 1,2-ANTHRAQUINONE DIAZIDE IN AROMATIC-HYDROCARBONS Full article

Journal

BULLETIN OF THE RUSSIAN ACADEMY OF SCIENCES-DIVISION OF CHEMICAL SCIENCE
ISSN: 1063-5211

Output data

Year: 1992, Volume: 41, Number: 4, Pages: 789-791 Pages count : 3 DOI: 10.1007/BF01150908

Tags

PHOTOLYSIS; 1,2-ANTHRAQUINONE DIAZIDE; AROMATIC HYDROCARBONS; ISOMERS

Authors

Klimenko L.S. ¹ , Mainagashev I.Ya. ¹ , Fokin E.P. ¹

Affiliations

1	Novosibirsk Institute of Organic Chemistry, Siberian Branch, Russian Academy of Sciences, Novosibirsk 630090

It has been determined that the main products of photolysis of 1,2-anthraquinone diazide in benzene, toluene, anisole, nitrobenzene, and pyridine are the corresponding 1-hydroxy-2-arylanthraquinones that form as a mixture of ortho, meta, and para isomers with significant content of the meta isomer (40-55%).

Klimenko L.S. , Mainagashev I.Y. , Fokin E.P.
PHOTOLYSIS OF 1,2-ANTHRAQUINONE DIAZIDE IN AROMATIC-HYDROCARBONS
BULLETIN OF THE RUSSIAN ACADEMY OF SCIENCES-DIVISION OF CHEMICAL SCIENCE. 1992. V.41. N4. P.789-791. DOI: 10.1007/BF01150908 WOS Scopus

Published print:

Apr 1, 1992

Web of science	WOS:A1992KB91200014
Scopus	2-s2.0-34249838627
OpenAlex	W2953148498