Methods of synthesis of alicyclic 1,5,9-triketones. Reaction of transaminomethylation
- Authors: Akimova T.I.1, Soldatkina O.A.1, Ivanenko Z.A.1, Savchenko V.G.1
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Affiliations:
- Far-Eastern Federal University
- Issue: Vol 53, No 5 (2017)
- Pages: 720-728
- Section: Article
- URL: https://bakhtiniada.ru/1070-4280/article/view/216204
- DOI: https://doi.org/10.1134/S1070428017050128
- ID: 216204
Cite item
Abstract
Alicyclic 1,5,9-triketones with various combination of 5-, 6-, 7-membereded cycles in the molecule were obtained by methods of diketone condensation, Michael reaction, and proceeding from Mannich mono- and bisbases and cycloalkanones. The latter method was accompanied with a transaminomethylation, observed for the first time at triketones preparation. The structures of cyclic forms of Michael reaction products were refined.
About the authors
T. I. Akimova
Far-Eastern Federal University
Author for correspondence.
Email: akimova.ti@dvfu.ru
Russian Federation, ul. Sukhanova 8, Vladivostok, 690091
O. A. Soldatkina
Far-Eastern Federal University
Email: akimova.ti@dvfu.ru
Russian Federation, ul. Sukhanova 8, Vladivostok, 690091
Zh. A. Ivanenko
Far-Eastern Federal University
Email: akimova.ti@dvfu.ru
Russian Federation, ul. Sukhanova 8, Vladivostok, 690091
V. G. Savchenko
Far-Eastern Federal University
Email: akimova.ti@dvfu.ru
Russian Federation, ul. Sukhanova 8, Vladivostok, 690091
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