Enhancement of benzylic basicity by a fluorine substituent at the para-position: A case of lone pair/lone pair repulsion

Chemistry - A European Journal

Volumn 6, Issue 5, 2000, Pages 771-777

  Faigl, Ferenc ^b   Marzi, Elena ^a   Schlosser, Manfred ^a  

^a UNIVERSITY OF LAUSANNE   (Switzerland)

^b BUDAPEST UNIVERSITY OF TECHNOLOGY AND ECONOMICS   (Hungary)

Author keywords

Acidity; Electron electron repulsion; Fluorine; Lithiation; Substituent effects

Indexed keywords

BENZYL DERIVATIVE; FLUORINE; TOLUENE;

ACIDITY; ALKALINITY; ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; ELECTRON TRANSPORT; ISOMERISM; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PROTON TRANSPORT;

EID: 0034599112     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/(sici)1521-3765(20000303)6:5<771::aid-chem771>3.0.co;2-g     Document Type: Article

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