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
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj/68/5/68_5_1409/_pdf
Reference48 articles.
1. Azulene analogues of triphenylmethyl cation; extremely stable hydrocarbon carbocations
2. Dynamic stereochemistry of tri(3-methyl-1-azulenyl)methyl cation; the first example of one-ring flip mechanism
3. Tris(3,6-di-t-butyl-1-azulenyl)methyl cation; hydrocarbon cation with the highest pKR+ value
4. 1,2:3,4:5,6-Tris(bicyclo[2.2.2]octeno)tropylium ion: an all-hydrocarbon carbocation with extraordinary stability
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