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This article is cited in 8 scientific papers (total in 8 papers)
Stereoselective synthesis of spirofused 3-substituted 2,3,4,4a,5,6-hexahydro- 6H-benzo[c]quinolizine using the tert-amino effect
E. V. Deevaa, T. V. Glukharevaa, A. V. Tkachevb, Yu. Yu. Morzherina a Department of Technology of Organic Synthesis, Urals State Technical University, Ekaterinburg, Russian Federation
b N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation
Abstract:
The interaction of 2-(4-R-piperidino)benzaldehyde and cyclic CH-active compounds occurred as a tandem of Knövenagel condensation and cyclization by tert-amino effect and led to spiro-fused 3-substituted 2,3,4,4a,5,6-hexahydro-6H-benzo[c]quinolizine.
Citation:
E. V. Deeva, T. V. Glukhareva, A. V. Tkachev, Yu. Yu. Morzherin, “Stereoselective synthesis of spirofused 3-substituted 2,3,4,4a,5,6-hexahydro- 6H-benzo[c]quinolizine using the tert-amino effect”, Mendeleev Commun., 16:2 (2006), 82–83
Linking options:
https://www.mathnet.ru/eng/mendc3529 https://www.mathnet.ru/eng/mendc/v16/i2/p82
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