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Synthesis of Amines from Norbornane Series

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Abstract

Synthetic procedure was developed for preparation of exo-oriented di- and tetraamines of the norbornane series by 1,3-dipolar cycloaddition to norbornene and norbornadiene of generated in situ diazomethane followed by reduction of arising pyrazolines catalyzed by Raney nickel.

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Authors and Affiliations

  1. Institute of Organic Chemistry, Ufa Scientific Center, Russian Academy of Sciences, Ufa, 450054, Russia

    E.A. Yatsynich, D.V. Petrov & V.A. Dokichev

  2. Zelinsky Institute of Organic Chemistry, Russian Academy of Science, Russia

    Yu.V. Tomilov

Authors
  1. E.A. Yatsynich
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  2. D.V. Petrov
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  3. V.A. Dokichev
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  4. Yu.V. Tomilov
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__________

Translated from Zhurnal Organicheskoi Khimii, Vol. 41, No. 8, 2005, pp. 1210–1214.

Original Russian Text Copyright © 2005 by Yatsynich, Petrov, Dokichev, Tomilov.

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Yatsynich, E., Petrov, D., Dokichev, V. et al. Synthesis of Amines from Norbornane Series. Russ J Org Chem 41, 1187–1191 (2005). https://doi.org/10.1007/s11178-005-0313-9

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  • DOI: https://doi.org/10.1007/s11178-005-0313-9

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