Hydrogen Bonding to Hexafluoroisopropanol Controls the Oxidative Strength of Hypervalent Iodine Reagents

Journal of the American Chemical Society

Volumn 138, Issue 28, 2016, Pages 8855-8861

  Colomer, Ignacio ^a   Batchelor Mcauley, Christopher ^a   Odell, Barbara ^a   Donohoe, Timothy J ^a   Compton, Richard G ^a  

^a UNIVERSITY OF OXFORD   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

FREE RADICAL REACTIONS; IODINE; SOLVENTS; STYRENE;

ENHANCED REACTIVITY; FLUORINATED SOLVENTS; HEXAFLUOROISOPROPANOL; HYPERVALENT IODINE; HYPERVALENT IODINE REAGENTS; OXIDIZING REAGENTS; SINGLE ELECTRON TRANSFER; [2+2] CYCLOADDITION;

HYDROGEN BONDS;

ACETONITRILE; ALKENE; ANETHOLE; CHEMICAL COMPOUND; CYCLOBUTANE; FERROCENE; HEXAFLUORO 2 PROPANOL; IODINE; PHENYLIODINE(III) DIACETATE; REAGENT; STYRENE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CYCLOADDITION; DIFFUSION ORDERED SPECTROSCOPY; DIMERIZATION; ELECTROCHEMICAL ANALYSIS; ELECTRON TRANSPORT; HYDROGEN BOND; MASS SPECTROMETRY; NUCLEAR OVERHAUSER EFFECT; NUCLEOPHILICITY; OXIDATION; OXIDATION REDUCTION POTENTIAL; OXIDATION REDUCTION REACTION; PROTON NUCLEAR MAGNETIC RESONANCE; SPECTROSCOPY; THERMODYNAMICS;

EID: 84979497620     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/jacs.6b04057     Document Type: Article

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