Lewis Acid-Catalyzed Rearrangement of 2,2-Dichloronorbornane to 1-Chloronorbornane-Reference-Cited by-同舟云学术

Lewis Acid-Catalyzed Rearrangement of 2,2-Dichloronorbornane to 1-Chloronorbornane

Published:2004-05-29 Issue:14 Volume:69 Page:4843-4844
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Smith Kenneth¹,Conley Nicie¹,Hondrogiannis George¹,Glover Lyle¹,Green James F.¹,Mamantov Andrew¹,Pagni Richard M.¹

Affiliation:

1. Department of Chemistry, University of Tennessee, Knoxville, Tennessee 37996-1600, and Environmental Protection Agency, 1200 Pennsylvania Avenue, Washington, D.C. 20460 %rpagni@utk.edu

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo030350e

Reference14 articles.

1. Stable Carbonium Ions. X.1 Direct Nuclear Magnetic Resonance Observation of the 2-Norbornyl Cation

2. Aromatic substitution. 63. Friedel-Crafts alkylation of aromatics with 1-chloronorbornane, 3-halonoradamantane, and fluorocubane via their reactive sp3-hybridized bridgehead carbocations

3. The Stability of Bridgehead Carbocations

4. Single Electron Transfer in Nucleophilic Aliphatic Substitution. Evidence for Single Electron Transfer in the Reactions of 1-Halonorbornanes with Various Nucleophiles

5. Effects of Bridgehead Substituents on the Stability of the 1-Norbornyl Radical

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