Electrofugalities of 1,3-Diarylallyl Cations-Reference-Cited by-同舟云学术

Electrofugalities of 1,3-Diarylallyl Cations

Published:2013-02-13 Issue:6 Volume:78 Page:2649-2660
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Troshin Konstantin¹,Mayr Herbert¹

Affiliation:

1. Department Chemie, Ludwig-Maximilians-Universität München, Butenandtstrasse 5-13 (Haus F), 81377 München, Germany

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo302766k

Reference57 articles.

1. More precisely, the generation of the free ions from a covalent substrate should be termed asionization plus dissociation:Reichardt, C.; Welton, T.Solvents and Solvent Effects in Organic Chemistry,4th ed.Wiley:Weinheim, 2011; p52.To avoid the long terms, we used the termheterolysisas a description of this process.

2. π-Nucleophilicity in Carbon−Carbon Bond-Forming Reactions

3. A Practical Guide for Estimating Rates of Heterolysis Reactions

4. Kinetics of the Solvolyses of Benzhydryl Derivatives: Basis for the Construction of a Comprehensive Nucleofugality Scale

5. Chem.—Eur. J. 2006, 12, 5415.

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