Syntheses and Properties of Extremely Stable Di(1-azulenyl)phenylmethyl and (1-Azulenyl)diphenylmethyl Cations Having Dimethylamino Substituents on Their Phenyl Groups-Reference-Cited by-同舟云学术

Syntheses and Properties of Extremely Stable Di(1-azulenyl)phenylmethyl and (1-Azulenyl)diphenylmethyl Cations Having Dimethylamino Substituents on Their Phenyl Groups

Published:1996-11 Issue:11 Volume:69 Page:3225-3237
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Ito Shunji,Kobayashi Hiroki,Kikuchi Shigeru,Morita Noboru,Asao Toyonobu

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/bcsj/69/11/69_11_3225/_pdf

Reference25 articles.

1. Azulene analogues of triphenylmethyl cation; extremely stable hydrocarbon carbocations

2. Tris(3,6-di-t-butyl-1-azulenyl)methyl cation; hydrocarbon cation with the highest pKR+ value

3. Syntheses of Azulene Analogues of Triphenylmethyl Cation: Extremely Stable Hydrocarbon Carbocations and the First Example of a One-Ring Flip as the Threshold Rotation Mechanism for Molecular Propellers

4. Dynamic stereochemistry of tri(2-methyl-1-azulenyl)methyl cation; steric effect of 2-methyl groups on rotational barriers and mechanism

5. Synthesis and Dynamic Stereochemistry of a Tri(1-azulenyl)methyl Cation Containing a Different Substituent on Each Azulene Ring

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5. Electrophilicipso-Substitution and Some Unique Reaction Behavior of 1,3,6-Tri-tert-butylazulene;European Journal of Organic Chemistry;2009-04