The Homoallyl-Cyclopropylcarbinyl Cation Rearrangement in the Solvolyses ofexo- andendo-5-Norbornen-2-ylp-Bromobenzenesulfonates. Application of2H-NMR. Spectroscopy-Reference-Cited by-同舟云学术

The Homoallyl-Cyclopropylcarbinyl Cation Rearrangement in the Solvolyses ofexo- andendo-5-Norbornen-2-ylp-Bromobenzenesulfonates. Application of2H-NMR. Spectroscopy

Published:1980-06-06 Issue:4 Volume:63 Page:1006-1015
ISSN:0018-019X
Container-title:Helvetica Chimica Acta
language:de
Short-container-title:Helv. Chim. Acta

Author:

Burger Ulrich,Sonney Jean-Marie,Vogel Pierre

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis

Reference57 articles.

1. Solvolytic Reactivities of Nortricyclyl, Dehydronorbornyl and Norbornyl Halides. Possible Steric Requirements for Hyperconjugative Resonance1

2. DRIVING FORCE OF THE HOMOALLYLIC REARRANGEMENT IN ACETOLYSIS OF exo-DEHYDRONORBORNYL p-BROMOBENZENESULFONATE1

3. Rearrangements in Carbonium Ion-Type Reactions of C14-Labeled Dehydronorbornyl Derivatives1

4. Bridged polycyclic compounds. LXXVI. Nature of the norbornenyl-nortricyclyl cation

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