Direct Benzylic CH Activation for CO Bond Formation by Photoredox Catalysis

Power of light: 1,4‐dicyanonaphthalene (DCN) and light directly activates benzylic CH bonds for intra‐ and intermolecular CO bond formation. Arylalkyls have also been transformed directly into aryl ketones using water as a source of oxygen. EDG=electron‐donating group, EWG=electron‐withdrawing gro...

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Veröffentlicht in:Angewandte Chemie International Edition 2013-05, Vol.52 (19), p.5146-5149
Hauptverfasser: Pandey, Ganesh, Pal, Sujit, Laha, Ramkrishna
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creator Pandey, Ganesh
Pal, Sujit
Laha, Ramkrishna
description Power of light: 1,4‐dicyanonaphthalene (DCN) and light directly activates benzylic CH bonds for intra‐ and intermolecular CO bond formation. Arylalkyls have also been transformed directly into aryl ketones using water as a source of oxygen. EDG=electron‐donating group, EWG=electron‐withdrawing group.
doi_str_mv 10.1002/anie.201210333
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subjects Activation
arenes
Aromatic compounds
Benzene Derivatives - chemistry
Bonding
Catalysis
CH activation
heterocycles
Ketones
Ketones - chemistry
Light
Molecular Structure
Naphthalenes - chemistry
Oxidation-Reduction
Oxygen - chemistry
photochemistry
Photoredox catalysis
reaction mechanisms
title Direct Benzylic CH Activation for CO Bond Formation by Photoredox Catalysis
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