Enantioselective photoredox catalysis enabled by proton-coupled electron transfer: Development of an asymmetric aza-pinacol cyclization

Journal of the American Chemical Society

Volumn 135, Issue 47, 2013, Pages 17735-17738

  Rono, Lydia J ^a   Yayla, Hatice G ^a   Wang, David Y ^a   Armstrong, Michael F ^a   Knowles, Robert R ^a  

^a PRINCETON UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

1 ,2-AMINO ALCOHOLS; ASYMMETRIC CATALYSIS; CATALYTIC PROTOCOL; DIASTEREO- AND ENANTIOSELECTIVITY; PHOTOREDOX CATALYSIS; POTENTIAL BENEFITS; PROTON-COUPLED ELECTRON TRANSFER; REDUCTIVE COUPLINGS;

BROMINE COMPOUNDS; CATALYSIS; ELECTRON TRANSITIONS; ENANTIOSELECTIVITY; KETONES; PROTONS; REACTION INTERMEDIATES;

FREE RADICAL REACTIONS;

AMINOALCOHOL; BRONSTED ACID; CARBON; CHEMICAL COMPOUND; HYDRAZONE DERIVATIVE; KETONE; KETYL; PHOSPHORIC ACID; UNCLASSIFIED DRUG;

ARTICLE; ASYMMETRIC AZA PINACOL CYCLIZATION; ASYMMETRIC CATALYSIS; CATALYSIS; CATALYST; CHEMICAL BINDING; CHEMICAL REACTION; CHEMICAL STRUCTURE; CYCLIZATION; ENANTIOSELECTIVITY; HYDROGEN BOND; OXIDATION REDUCTION REACTION; PHOTOREACTIVITY; PHOTOREDOX CATALYSIS; PROTON COUPLED ELECTRON TRANSFER; STEREOCHEMISTRY;

EID: 84889246295     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja4100595     Document Type: Article

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