trans-3-Aryl-4-nitro-pyrrolidines via 1,3-dipolar cycloaddition of nonstabilized azomethine ylide to ß-nitro styrenes

Miklós Nyerges, László Balázs, István Kádas, István Bitter, István Kövesdi, László Tőke

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31 Citations (Scopus)

Abstract

Various β-nitro styrenes undergo 1,3 dipolar cycloaddition with the azomethine ylide derived from sarcosine and paraformaldehyde to give 3-aryl-4-nitro-pyrrolidines in good yield.

Original languageEnglish
Pages (from-to)6783-6788
Number of pages6
JournalTetrahedron
Volume51
Issue number24
DOIs
Publication statusPublished - Jun 12 1995

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ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

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