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1,3-Dipolar Cycloadditions VI [1].Structure and Conformation of Cycloadducts from Reactions of C-Aryl-N-phenylnitrones with Substituted Cinnamic Acid Amides

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Summary.

 Studies on cycloadditions of C,N-diarylnitrones to cinnamic acid amides were carried out. The diastereoisomeric (I, II) and (in some cases) regioisomeric (III) cycloadducts obtained were characterized by spectroscopic and X-ray data. Conformational studies were carried out by molecular modelling.

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Authors and Affiliations

  1.  Centre of Advanced Studies on Natural Products, Department of Chemistry, Calcutta University, Calcutta-700009, India, , , , , , IN

    Avijit Banerji, Kaustabh Kumar Maiti, Sunanda Haldar, Chaitali Mukhopadhyay & Julie Banerji

  2.  Laboratoire de Chimie Structurale Biomoleculaire, Université Paris Nord, F-93012 Bobigny, France, , , , , , FR

    Thierry Prangé & Alain Neuman

Authors
  1. Avijit Banerji
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  2. Kaustabh Kumar Maiti
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  3. Sunanda Haldar
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  4. Chaitali Mukhopadhyay
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  5. Julie Banerji
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  6. Thierry Prangé
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  7. Alain Neuman
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Received February 8, 2000. Accepted February 18, 2000

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Banerji, A., Maiti, K., Haldar, S. et al. 1,3-Dipolar Cycloadditions VI [1].Structure and Conformation of Cycloadducts from Reactions of C-Aryl-N-phenylnitrones with Substituted Cinnamic Acid Amides. Monatshefte fuer Chemie 131, 901–911 (2000). https://doi.org/10.1007/s007060070068

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  • DOI: https://doi.org/10.1007/s007060070068

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