Synthesis of spiro[pyrrole-3,2'-pyrrolo[2,1-b]oxazoles] via 1,3-dipolar cycloaddition of 1H-pyrrole-2,3-diones to azomethine ylides

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Resumo

The 1,3-dipolar cycloaddition of 1 H -pyrrole-2,3-diones to azomethine ylides obtained in situ by the condensation of L-proline and arylcarbaldehydes proceeds regio- and diastereoselectively and leads to the formation of substituted ethyl 1,2,5',6',7',7a'-hexahydro-3' H -spiro[pyrrole-3,2'-pyrrolo[2,1- b ]oxazole]-4-carboxylates. The structure of one of the obtained compounds was confirmed by single crystal X-ray analysis.

Sobre autores

A. Moroz

Perm State University

M. Dmitriev

Perm State University

A. Maslivets

Perm State University

Email: koh2@psu.ru

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