Why the Classical and Nonclassical Norbornyl Cations Do Not Resemble the 2-endo- and 2-exo-Norbornyl Solvolysis Transition States1,-Reference-Cited by-同舟云学术

Why the Classical and Nonclassical Norbornyl Cations Do Not Resemble the 2-endo- and 2-exo-Norbornyl Solvolysis Transition States1,

Published:1997-06-01 Issue:13 Volume:62 Page:4216-4228
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Schreiner Peter R.¹,Schleyer Paul von Ragué¹,Schaefer Henry F.¹

Affiliation:

1. Center for Computational Quantum Chemistry, University of Georgia, Athens, Georgia 30602, and Computer Chemistry Center, Institut für Organische Chemie der Universität Erlangen-Nürnberg, Henkestr. 42, D-91054 Erlangen, Germany

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo9613388

Reference83 articles.

1. This paper was presented at the KISPOC VII in Japan, 1995.

2. THE STRUCTURE OF THE BICYCLO[2,2,1]2-HEPTYL (NORBORNYL) CARBONIUM ION

3. The Nonclassical Ion Problem

4. Remote inductive effects in the solvolysis of secondary and tertiary 2-norbornyl derivatives. Evidence for nonclassical stabilization of the 2-norbornyl cation

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