Facile heterolysis of a carbon-carbon bond. Arylazodicyanomethanides as the leaving group capable of generating tert-cumyl cation and the hydrogen-bond-insusceptible behavior of the leaving group anions-Reference-Cited by-同舟云学术

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Facile heterolysis of a carbon-carbon bond. Arylazodicyanomethanides as the leaving group capable of generating tert-cumyl cation and the hydrogen-bond-insusceptible behavior of the leaving group anions

Published:1986-04 Issue:9 Volume:108 Page:2394-2400
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Mitsuhashi Tsutomu.

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja00269a042

Cited by 22 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. Acid-promoted SN1/E1 fragmentation/dimerization of 2-cumylmalonates;Tetrahedron Letters;2009-06

2. Solvation effects in the heterolyses of 3‐X‐3‐methylpentanes (X = Cl, Br, I);Journal of Physical Organic Chemistry;2004-07-27

3. Kinetics and mechanism of monomolecular heterolysis of commercial organohalogen compounds: XXIX. Solvent effects on the activation parameters of heterolysis of tert-butyl chloride;Russian Journal of General Chemistry;2002

4. Ionic Dissociation of Carbon—Carbon σ Bonds in Hydrocarbons and the Formation of Authentic Hydrocarbon Salts;Advances in Physical Organic Chemistry;1995

5. Quantitative Analysis of Solvent Effects on the Rate of Heterolysis Reactions: Relative Importance of Cation and Anion Solvation;Bulletin of the Chemical Society of Japan;1994-03

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