The 3,5-dichloro-4-cyanophenyl group. a useful moiety for the extension of ϱσ+ studies.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference10 articles.
1. Solvolysis of Substituted 2-Aryl-exo-norbornyl Chlorides. Application of the Hammett Correlation as a Test for σ Participation in the Norbornyl System
2. Unusually high exo:endo rate ratios in the solvolysis of 2-p-anisylcamphenilyl p-nitrobenzoates and related compounds. Further evidence for steric effects as a major factor in the exo:endo rate ratios of tertiary norbornyl derivatives
3. Predominant exo substitution in the products from the solvolysis of 2-p-anisylcamphenilyl p-nitrobenzoates and related compounds. Further evidence for steric effects as a major factor in the exo:endo product ratios from tertiary norbornyl derivatives
4. Aryl delocalization vs. neighboring group participation in the stabilization of carbonium ions
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1. Studies on Long-Lived (Pentafluorosulfanyl)phenyl-Substituted Carbocations;The Journal of Organic Chemistry;2019-09-10
2. Organoalkali Chemistry;Organometallics in Synthesis: A Manual;2013-06-26
3. ChemInform Abstract: DIE 3,5-DICHLOR-4-CYANPHENYL-GRUPPIERUNG, EINE GEEIGNETE GRUPPRIERUNG ZUR ERWEITERUNG VON RHO, SIGMA(+)-UNTERSUCHUNGEN;Chemischer Informationsdienst. Organische Chemie;1970-07-07
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