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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2011 Volume 21, Issue 4, Pages 231–233 (Mi mendc2927)

This article is cited 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.

Language: English

DOI: 10.1016/j.mencom.2011.07.021



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