Neue Methode zur reduktiven Desaminierung primärer aliphatischer Amine

Authors

  • Thomas Wirth Institut für Organische Chemie und Biochemie Albert-Ludwigs-Universität Albertstrasse 21, D-7800 Freiburg i. Br. (Bundesrepublik Deutschland)
  • Christoph Rüchardt Institut für Organische Chemie und Biochemie Albert-Ludwigs-Universität Albertstrasse 21, D-7800 Freiburg i. Br. (Bundesrepublik Deutschland)

DOI:

https://doi.org/10.2533/chimia.1988.230

Abstract

A new method for reductive deamination of primary aliphatic amines via tributyltin hydride reduction of aromatic imidoyl chlorides is reported. Good yields of hydrocarbons were obtained from benzylamines and cyclohexylamine, but not from 1-alkylamines.

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Published

1988-06-30

Issue

Vol. 42 No. 6 (1988): Forschung/Research

Section

Articles

License

Copyright (c) 1988 Thomas Wirth

Creative Commons License

This work is licensed under a Creative Commons Attribution 4.0 International License.

How to Cite

[1]
T. Wirth, C. Rüchardt, Chimia 1988, 42, 230, DOI: 10.2533/chimia.1988.230.