A theoretical (DFT, GIAO-NMR, NICS) study of the carbocations and oxidation dications from azulenes, homoazulene, benzazulenes, benzohomoazulenes, and the isomeric azulenoazulenes-Reference-Cited by-同舟云学术

A theoretical (DFT, GIAO-NMR, NICS) study of the carbocations and oxidation dications from azulenes, homoazulene, benzazulenes, benzohomoazulenes, and the isomeric azulenoazulenes

Published:2003 Issue:17 Volume:1 Page:3078-3093
ISSN:1477-0520
Container-title:Org. Biomol. Chem.
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Okazaki Takao,Laali Kenneth K.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2003/OB/B303865C

Reference30 articles.

1. The sulfonation and protonation of a series of azulenes. Observation of stable σ-complexes in the sulfonation of 4,6,8-trimethylazulene, guaiazulene and bis(3-guaiazulenyl)methane

2. Generation, Characterization and Some Reactions of 1,1-Ethylene-1H-azulenium Ion

3. Synthesis and stability of 1,1-tetramethylene- and 1,1-pentamethylene-1H-azulenium ions

4. Dispiro[cyclohexane-1,1′-(1′,7′-dihydrocyclopenta[f]azulenium)-7′,1′′-cyclohexane] perchlorate, a new highly stable hydrocarbon cation

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