M. A. Mironov, M. I. Kleban, V. S. Mokrushin, “Stereoselective synthesis of 2-pyrrolinyl- and 2-imidazolinylthiazoles”, Mendeleev Commun., 9:3 (1999), 118

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Mendeleev Communications, 1999, Volume 9, Issue 3, Pages 118–119
DOI: https://doi.org/10.1070/MC1999v009n03ABEH001082 (Mi mendc4553)

This article is cited in 1 scientific paper (total in 1 paper)

Stereoselective synthesis of 2-pyrrolinyl- and 2-imidazolinylthiazoles

M. A. Mironov, M. I. Kleban, V. S. Mokrushin

Department of Technology of Organic Synthesis, Urals State Technical University, Ekaterinburg, Russian Federation

Full-text PDF (141 kB) Citations (1)

DOI: https://doi.org/10.1070/MC1999v009n03ABEH001082

Abstract: The reaction of 2-isocyanomethylthiazoles with trans-chalcone or aromatic azomethines in the presence of copper compounds results in only trans-pyrrolines or trans-imidazolines with thiazole substituents, as evidenced by ¹H NMR and mass spectrometry.

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Document Type: Article

Language: English

Citation: M. A. Mironov, M. I. Kleban, V. S. Mokrushin, “Stereoselective synthesis of 2-pyrrolinyl- and 2-imidazolinylthiazoles”, Mendeleev Commun., 9:3 (1999), 118–119

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https://www.mathnet.ru/eng/mendc/v9/i3/p118

This publication is cited in the following 1 articles:

Citing articles in Google Scholar: Russian citations, English citations
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