Solvolysis of 3-substituted 4-homoadamantyl methanesulphonates. Can the ?-substituent effect distinguish between classical and non-classical ion intermediates?-Reference-Cited by-同舟云学术

Solvolysis of 3-substituted 4-homoadamantyl methanesulphonates. Can the ?-substituent effect distinguish between classical and non-classical ion intermediates?

Published:1994-09 Issue:9 Volume:7 Page:485-494
ISSN:0894-3230
Container-title:Journal of Physical Organic Chemistry
language:en
Short-container-title:J. Phys. Org. Chem.

Author:

Okazaki Takao,Kitagawa Toshikazu,Takeuchi Ken'Ichi

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference36 articles.

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

2. Neighboring Carbon and Hydrogen. X. Solvolysis of endo-Norbornyl Arylsulfonates1,2,3

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

4. Inductivity and bridging in carbocations

5. The energy of the transition states and the intermediate cation in the ionization of 2-norbornyl derivatives. Where is the nonclassical stabilization energy?

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