Schmidt-Reaktion an Tetrahydro-chinolon-Derivaten

Authors

  • H.P. Härter Forschungsinstitut Wander AG, Bern
  • U. Stauss Forschungsinstitut Wander AG, Bern
  • J.H. Osiecki Forschungsinstitut Wander AG, Bern
  • O. Schindler Forschungsinstitut Wander AG, Bern

DOI:

https://doi.org/10.2533/chimia.1976.50

Abstract

The synthesis of the Tetrahydro-quinolones incorporated in indoles (I, II, III), carbazoles (VII, VIII) and tetrahydrocarbazoles (XIII, XIV) is described. The Schmidt-reaction under standardised conditions of the quinolones goes specifically to the 1,4-Diazepinderivatives IV, V, IX, X, XV and XVI. The analogous ketone derived from phenanthridone, XIX gives under the same experimental conditions the derivative of 1,4-Diazepine XXI as well as the 1,5-Diazepine XX.

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Published

1976-02-29

Issue

Vol. 30 No. 2 (1976): Forschung/Research

Section

Articles

License

Copyright (c) 1976 H.P. Härter

Creative Commons License

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

How to Cite

[1]
H. Härter, U. Stauss, J. Osiecki, O. Schindler, Chimia 1976, 30, 50, DOI: 10.2533/chimia.1976.50.