Aromatische Übergangszustände und die Reaktivität geometrisch wohldefinierter Moleküle

Authors

  • C.W. Jefford Département de Chimie Organique, Université de Genève, 1211 Genève 4
  • U. Burger Département de Chimie Organique, Université de Genève, 1211 Genève 4

DOI:

https://doi.org/10.2533/chimia.1971.297

Abstract

The qualitative concept of aromatic transition states is illustrated by reactions in which the reactant molecules possess well-defined geometry. Examples have been selected to show how the interplay between the orbital topology required and the skeletal constraints imposed by the transition state determine the stereochemical outcome of the reaction.

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Published

1971-09-30

Issue

Vol. 25 No. 9 (1971): Forschung/Research

Section

Articles

License

Copyright (c) 1971 C.W. Jefford

Creative Commons License

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

How to Cite

[1]
C. Jefford, U. Burger, Chimia 1971, 25, 297, DOI: 10.2533/chimia.1971.297.