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Synthesis of heterocyclic compounds using basic zeolite Csβ Full article

Journal Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353
Output data Year: 2009, Volume: 45, Number: 5, Pages: 560-566 Pages count : 7 DOI: 10.1007/s10593-009-0296-5
Tags 1,2,4-triazole-3-thiol; 5-methoxybenzimidazole-2-thiol; Basic zeolite; Heterogeneous catalysis; Methyl vinyl ketone; Michael addition
Authors Suslov E.V. 1 , Korchagina D.V. 1 , Volcho K.P. 1 , Salakhutdinov N.F. 1
Affiliations
1 N. N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences

Abstract: The application of the basic zeolite Csβ as catalyst for the interaction of methyl vinyl ketone (MVK) with 5-methoxybenzimidazole-2-thiol leads to a Michael heteroreaction exclusively at the N-nucleophilic center with the formation of a fairly unusual product of di-addition of MVK to thiol. The reaction of 1,2,4-triazole-3-thiol with MVK in the presence of zeolite Csβ proceeds both at the S- and also at the N-nucleophilic center and leads to the formation of products of mono- and diaddition according to Michael, and also to the product of heterocyclization. On interacting crotonaldehyde with salicylaldehyde in the presence of Csβ 2-methyl-2H-chromene-3-carbaldehyde is formed.
Cite: Suslov E.V. , Korchagina D.V. , Volcho K.P. , Salakhutdinov N.F.
Synthesis of heterocyclic compounds using basic zeolite Csβ
Chemistry of Heterocyclic Compounds. 2009. V.45. N5. P.560-566. DOI: 10.1007/s10593-009-0296-5 WOS Scopus РИНЦ OpenAlex
Dates:
Published print: May 1, 2009
Published online: Aug 21, 2009
Identifiers:
Web of science: WOS:000269529600008
Scopus: 2-s2.0-69949181583
Elibrary: 15300028
OpenAlex: W2027930415
Citing:
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Web of science 2
Scopus 2
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OpenAlex 3
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