Synthesis and oxidative transformations of 5,7-bis(4-methoxyphenil)-1,2,3,4,4a,5-hexahydro-13H-benzimidazo[2,1-j]-quinoline
- Authors: Harchenko L.N.1, Мaslov К.V.1, Slabko О.Y.1
 - 
							Affiliations: 
							
- Far-Eastern Federal University
 
 - Issue: Vol 60, No 12 (2024)
 - Pages: 1222-1228
 - Section: Articles
 - URL: https://clinpractice.ru/0514-7492/article/view/681815
 - DOI: https://doi.org/10.31857/S0514749224120066
 - EDN: https://elibrary.ru/AQBDPF
 - ID: 681815
 
Cite item
Abstract
1,5-Diketone, obtained by the reaction of 4,4′-dimethoxychalcone with cyclohexanone, interacts with o-phenylenediamine to give 5,7-bis(4-methoxyphenyl)-1,2,3,4,4,4a,5-hexahydro-13H-benzimidazo[2,1-j]quinoline. Oxidation and oxidative coupling reactions with some primary amines and benzoylacetonitrile have been studied, resulting in the formation of heterocyclic p-quinonoid compounds.
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About the authors
L. N. Harchenko
Far-Eastern Federal University
														Email: slabko.oyu@dvfu.ru
				                					                																			                												                	Russian Federation, 							Universitetskii pr., L901, Russky Island, Vladivostok, 690922						
К. V. Мaslov
Far-Eastern Federal University
														Email: slabko.oyu@dvfu.ru
				                	ORCID iD: 0000-0001-6760-2733
				                																			                												                	Russian Federation, 							Universitetskii pr., L901, Russky Island, Vladivostok, 690922						
О. Yu. Slabko
Far-Eastern Federal University
							Author for correspondence.
							Email: slabko.oyu@dvfu.ru
				                	ORCID iD: 0000-0002-4463-1555
				                																			                												                	Russian Federation, 							Universitetskii pr., L901, Russky Island, Vladivostok, 690922						
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