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ЖУРНАЛЫ // Mendeleev Communications // Архив

Mendeleev Commun., 2015, том 25, выпуск 6, страницы 440–442 (Mi mendc2438)

Эта публикация цитируется в 8 статьях

Communications

A novel synthesis of 2-alkyl(aryl)pyrrolidines from proline via 2,3-diphenylhexahydropyrrolo[2,1-b]oxazoles

V. S. Moshkin, V. Ya. Sosnovskikh

Department of Chemistry, Ural Federal University, Ekaterinburg, Russian Federation


Аннотация: Diphenyloxapyrrolizidines, products of the reaction between proline and benzaldehyde, are convenient building blocks for synthesizing 2-substituted pyrrolidines. The opening of their oxazolidine ring by treatment with Grignard reagents has been performed and conditions for subsequent removal of the N-hydroxyethyl moiety have been found. Though the yields are moderate (36–42%), the suggested synthesis of 2-alkyl(aryl)pyrrolidines is rather simple since it does not require purification of intermediate products and is easy scalable.

Язык публикации: английский

DOI: 10.1016/j.mencom.2015.11.014



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