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Angewandte Chemie - International Edition

Volumn 56, Issue 25, 2017, Pages 7191-7194

Mild, Redox-Neutral Formylation of Aryl Chlorides through the Photocatalytic Generation of Chlorine Radicals

(6) Nielsen, Matthew K a Shields, Benjamin J a Liu, Junyi a Williams, Michael J b Zacuto, Michael J b Doyle, Abigail G a

a PRINCETON UNIVERSITY (United States)

b CELGENE CORPORATION (United States)

Author keywords

C H functionalization; formylation; nickel; photocatalysis; redox reactions

Indexed keywords

CARBON MONOXIDE; CARBONYLATION; CATALYSIS; CHLORINE; CHLORINE COMPOUNDS; NICKEL; PHOTOCATALYSIS;

1 ,3-DIOXOLANE; CHLORINE RADICALS; FORMYLATION; FUNCTIONALIZATIONS; PHOTO-CATALYTIC; PHOTOREDOX CATALYSIS; PRESSURIZED GAS; REDUCTIVE CARBONYLATION;

REDOX REACTIONS;

1,3 DIOXOLANE DERIVATIVE; CHLORIDE; CHLORINE; FORMAL GLYCOL; FREE RADICAL; NICKEL;

CATALYSIS; CHEMISTRY; OXIDATION REDUCTION REACTION; PHOTOCHEMISTRY;

CATALYSIS; CHLORIDES; CHLORINE; DIOXOLANES; FREE RADICALS; NICKEL; OXIDATION-REDUCTION; PHOTOCHEMICAL PROCESSES;

EID: 85019587489 PISSN: 14337851 EISSN: 15213773 Source Type: Journal
DOI: 10.1002/anie.201702079 Document Type: Article

Times cited : (171)

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