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This article is cited in 8 scientific papers (total in 8 papers)
Reaction of 1-(oxiran-2-ylmethyl)-1H-indole-3-carboxaldehyde with amines
K. F. Suzdaleva, S. V. Den'kinaa, A. A. Starikovaa, V. V. Dvurechenskya, M. E. Kletskiib, O. N. Burovb a Institute of Physical and Organic Chemistry, Southern Federal University, Rostov-on-Don, Russian Federation
b Department of Chemistry, Southern Federal University, Rostov-on-Don, Russian Federation
Abstract:
Interaction of 1-(oxiran-2-ylmethyl)-1H-indole-3-carboxaldehyde with primary amines occurs at oxirane moiety and leads to b-aminoalcohols. Quantum-chemical calculations show that these products are more stable than possible alternative Schiff bases arising from aldehyde group of the considered bielectrophiles.
Citation:
K. F. Suzdalev, S. V. Den'kina, A. A. Starikova, V. V. Dvurechensky, M. E. Kletskii, O. N. Burov, “Reaction of 1-(oxiran-2-ylmethyl)-1H-indole-3-carboxaldehyde with amines”, Mendeleev Commun., 21:4 (2011), 231–233
Linking options:
https://www.mathnet.ru/eng/mendc2927 https://www.mathnet.ru/eng/mendc/v21/i4/p231
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