Predominant exo substitution in the products from the solvolysis of 2-p-anisylcamphenilyl p-nitrobenzoates and related compounds. Further evidence for steric effects as a major factor in the exo:endo product ratios from tertiary norbornyl derivatives-Reference-Cited by-同舟云学术

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Predominant exo substitution in the products from the solvolysis of 2-p-anisylcamphenilyl p-nitrobenzoates and related compounds. Further evidence for steric effects as a major factor in the exo:endo product ratios from tertiary norbornyl derivatives

Published:1968-09 Issue:19 Volume:90 Page:5270-5272
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Takeuchi Kenichi,Brown Herbert C.

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja01021a040

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Structural effects in solvolytic reactions. 21. Solvolysis of 2-aryl-2-norbornyl and 2-aryl-2-camphenilyl p-nitrobenzoates. Critical examination of the importance of .sigma.-participation in the solvolysis of tertiary 2-norbornyl derivatives by the application of the tool of increasing electron demand;Journal of the American Chemical Society;1977-04

2. Stabilized 2-Norbornyl Cations;The Nonclassical Ion Problem;1977

3. Explorations in the nonclassical ion area;Tetrahedron;1976-01

4. Stable carbocations. CLXVI. Benzonortricyclyl cations;Journal of the American Chemical Society;1975-04

5. Acetolysis products from some phenylnorbornyl tosylates;The Journal of Organic Chemistry;1973-11

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