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Selective Oxidation of Organic Compounds—Sustainable Catalytic Reactions with Oxygen and without Transition Metals?
Author(s) -
Lenoir Dieter
Publication year - 2006
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.200502702
Subject(s) - catalysis , transition metal , oxygen , oxide , chemistry , molecular oxygen , pollutant , inorganic chemistry , catalytic oxidation , redox , organic chemistry
Going without : Alcohols can be oxidized with oxygen and without transition‐metal complexes (see scheme; TEMPO=2,2,6,6‐tetramethylpiperidine‐N‐oxide). Conventional methods are compared with new catalytic variants developed for this reaction and for the complete oxidation of pollutants with regard to sustainability.

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