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Mendeleev Communications, 2011, Volume 21, Issue 4, Pages 231–233
DOI: https://doi.org/10.1016/j.mencom.2011.07.021
(Mi mendc2927)
 

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.
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (167.7 Kb)


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
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  • https://www.mathnet.ru/eng/mendc2927
  • https://www.mathnet.ru/eng/mendc/v21/i4/p231
  • This publication is cited in the following 8 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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