A Transition Metal Catalyzed Reaction of Aromatic Acyl Chlorides with Epoxides

Authors

  • Achim Roloff Central Research Laboratories Ciba-Geigy AG, CH-4002 Basel

DOI:

https://doi.org/10.2533/chimia.1985.392

Abstract

In a transition metal catalyzed reaction of aroyl chlorides with epoxides a change from palladium to ruthenium brings about a change in regioselectivity. A participation of the transition metal in the ring opening step is now evident.

Downloads

Published

1985-12-31

Issue

Vol. 39 No. 12 (1985): Forschung/Research

Section

Articles

License

Copyright (c) 1985 Achim Roloff

Creative Commons License

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

How to Cite

[1]
A. Roloff, Chimia 1985, 39, 392, DOI: 10.2533/chimia.1985.392.