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Organic reactions / Halogens / Electrophilic fluorination / Organofluorine chemistry / Electrophile / Halogenation / Xenon difluoride / Fluorine / Hydrogen fluoride / Chemistry / Fluorides / Organofluorides


Revue Roumaine de Chimie, 2007, 52(3), 219–234 REVIEW
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Document Date: 2008-08-11 19:05:16


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anhydrous HF. / Mitsui Chemicals / Daikin Industries / DuPont / ACS / Daiichi Pharmaceutical Company / O O R R LDA / /

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Germany / United States / /

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Swiss Federal Institute of Technology / University of Bonn / University of Southern California / University of Nebraska / Loker Hydrocarbon Research Institute / Institute of Organic Chemistry / /

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chemical yields / activated ring systems / trifluoromethyl / prochiral metal enolates / active pharmaceutical / electronics applications / pharmaceutical industry / enantioselective fluorination systems / metal catalysts / chemical fluorination / magnesium metal / fluorinated chemicals / high carbon-fluorine bond energy / fluorinated materials / transition-metal catalysts / transition-metal catalyst/fluorinating reagent combinations / difluoro products / /

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Loker Hydrocarbon Research Institute / Institute of Organic Chemistry / University of Southern California / Swiss Federal Institute of Technology / Zurich / the University of Nebraska / Lincoln / Roumanian Academy / University of Bonn / Department of Chemistry / /

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George A. Olah / Antonio Togni / Ingo Ruppert / Satoshi Takei / /

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