Exalted Resonance Effect in the Aryl-Assisted Solvolyses of 2-Aryl-2-(trifluoromethyl)ethylm-Nitrobenzenesulfonates
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/26/10/26_10_973/_pdf
Reference21 articles.
1. Destabilized Carbocations
2. Electronegatively substituted carbocations
3. Substituent Effect Studies of Aryl-Assisted Solvolyses. II. The Acetolysis of 2-Phenyl-2-(substituted phenyl)ethylp-Toluenesulfonates
4. The accurate C2v phenonium and benzenonium ion structures confirmed by correlated GIAO-MP2 NMR chemical shift calculations
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1. Kinetic Evidence for Dihapto (η2) π-Aryl Participation in Acid-Catalyzed Ring Opening of Diarylhomobenzoquinone Epoxides;The Journal of Organic Chemistry;2009-12-21
2. Exalted Resonance Demands in the Substituent Effects on the Acetolyses of 2-Arylethyl Trifluoromethanesulfonates Destabilized by CN and CF3Groups;Bulletin of the Chemical Society of Japan;2009-02-15
3. Thermodynamic stabilities of propylenebenzenium ions in the gas phase. Substituent effect of unsymmetrical phenonium ions;Arkivoc;2008-04-25
4. Mechanistic evidence for remote π-aryl participation in acid-catalyzed ring opening of homobenzoquinone epoxides;Chemical Communications;2008
5. Kinetic Evidence for Remote π-Aryl Participation in the BF3-Catalyzed Rearrangement of [2 + 2] Photocycloadducts of Diarylhomobenzoquinones with Diphenylacetylene;Organic Letters;2004-10-01
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