Selective Photocyclization of Amino Acids in Dipeptides

Authors

  • Stephan Sauer
  • Christian Staehelin
  • Caroline Wyss
  • Bernd Giese

DOI:

https://doi.org/10.2533/chimia.1997.23

Abstract

Amino acids in dipeptides which are substituted at the N-atom by a benzoylalkyl group can be selectively photocyclized via a triplet biradical. With valine as amino acid the cyclization leads mainly to one product out of eight possible isomers.

Downloads

Published

1997-02-26

How to Cite

[1]
S. Sauer, C. Staehelin, C. Wyss, B. Giese, Chimia 1997, 51, 23, DOI: 10.2533/chimia.1997.23.

Issue

Vol. 51 No. 1-2 (1997): ILMAC 96 Retrospective

Section

Scientific Articles

License

Copyright (c) 1997 Swiss Chemical Society

Creative Commons License

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