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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2020 Volume 30, Issue 3, Pages 350–351 (Mi mendc1194)

This article is cited in 7 papers

Communications

Synthesis of new alkoxy/alkylthiovinylated oxazoles using tosylmethyl isocyanide

N. V. Vchislo, V. G. Fedoseeva, V. V. Novokshonov, L. I. Larina, I. B. Rosentsveig, E. A. Verochkina

A.E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, Irkutsk, Russian Federation

Abstract: The reaction of 2-alkoxy- and 2-alkylthio-3-(het)arylpropenals with tosylmethyl isocyanide affords oxazoles bearing the corresponding 5-positioned 1-alkylchalcogenyl-2-(het)arylvinyl groups.

Keywords: vinyl ethers, vinyl sulfides, enals, oxazoles, heterocyclization, isocyanides, tosylmethyl isocyanide.

Language: English

DOI: 10.1016/j.mencom.2020.05.030



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