Journal ArticleOPEN ACCESS

Asymmetric 1,3-Dipolar Cycloadditons of Stabilized Azomethine Ylides with Nitroalkenes

  • Nejera C
  • Sansano J
Current Topics in Medicinal Chemistry (2014) 14(10) 1271-1282
DOI: 10.2174/1568026614666140423112145
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Abstract

This review highlights the biological importance of many polysubstituted nitro-prolines and -pyrrolidines. Their preparation using asymmetric 1,3-dipolar cycloadditions of azomethine ylides with nitroalkenes using diastereose-lective and enantioselective strategies is described remarking the scope and main features of each one. © 2014 Bentham Science Publishers.

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APA

Nejera, C., & Sansano, J. (2014). Asymmetric 1,3-Dipolar Cycloadditons of Stabilized Azomethine Ylides with Nitroalkenes. Current Topics in Medicinal Chemistry, 14(10), 1271–1282. https://doi.org/10.2174/1568026614666140423112145

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