Email this article Isomerization of 4-arylamino-1,2-naphthoquinones to 2-arylamino-1,4-naphthoquinones
- Authors: Gornostaev L.M.1, Rukovets T.A.1,2, Lavrikova T.I.1, Khalyavina Y.G.1, Stashina G.A.3
-
Affiliations:
- Krasnoyarsk State Pedagogical University named after V. P. Astafyev
- Krasnoyarsk State Medical University named after Prof. V. F. Voino-Yasenetsky
- N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
- Issue: Vol 66, No 6 (2017)
- Pages: 1007-1010
- Section: Full Articles
- URL: https://ogarev-online.ru/1066-5285/article/view/240710
- DOI: https://doi.org/10.1007/s11172-017-1847-z
- ID: 240710
Cite item
Open Access
Access granted
Subscription Access
Abstract
4-Arylamino-1,2-naphthoquinones isomerize into 2-arylamino-1,4-naphthoquinones upon refluxing in acetic acid. The isomerization follows two routes via intermediate 2-hydroxy-1,4-naphthoquinone and 2-arylamino-1,4-naphthoquinone 4-N-arylimines.
About the authors
L. M. Gornostaev
Krasnoyarsk State Pedagogical University named after V. P. Astafyev
Author for correspondence.
Email: gornostaev@kspu.ru
Russian Federation, 89 ul. Ady Lebedevoi, Krasnoyarsk, 660049
T. A. Rukovets
Krasnoyarsk State Pedagogical University named after V. P. Astafyev; Krasnoyarsk State Medical University named after Prof. V. F. Voino-Yasenetsky
Email: gornostaev@kspu.ru
Russian Federation, 89 ul. Ady Lebedevoi, Krasnoyarsk, 660049; 1 ul. Partizana Zheleznyaka, Krasnoyarsk, 660021
T. I. Lavrikova
Krasnoyarsk State Pedagogical University named after V. P. Astafyev
Email: gornostaev@kspu.ru
Russian Federation, 89 ul. Ady Lebedevoi, Krasnoyarsk, 660049
Yu. G. Khalyavina
Krasnoyarsk State Pedagogical University named after V. P. Astafyev
Email: gornostaev@kspu.ru
Russian Federation, 89 ul. Ady Lebedevoi, Krasnoyarsk, 660049
G. A. Stashina
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Email: gornostaev@kspu.ru
Russian Federation, 47 Leninsky prosp., Moscow, 119991
Supplementary files
