An unusual chemoselective hydrogenation of quinoline compounds using supported gold catalysts

Journal of the American Chemical Society

Volumn 134, Issue 42, 2012, Pages 17592-17598

  Ren, Dong ^a   He, Lin ^a   Yu, Lei ^a   Ding, Ran Sheng ^a   Liu, Yong Mei ^a   Cao, Yong ^a   He, He Yong ^a   Fan, Kang Nian ^a  

^a FUDAN UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

CATALYST SYSTEM; CATALYTIC HYDROGENATION; CATALYTIC PROCESS; CHEMICAL TRANSFORMATIONS; CHEMOSELECTIVE HYDROGENATION; FUNCTIONALIZED; GOLD CATALYSIS; GOLD NANOPARTICLES; HETEROCYCLIC RINGS; HYDROGENATION REACTIONS; ISOQUINOLINES; MILD REACTION CONDITIONS; PROMOTIONAL EFFECT; QUINOLINE COMPOUNDS; REACTANT MOLECULES; REGIOSPECIFIC; SUPPORTED GOLD; SUPPORTED GOLD CATALYSTS; SUSTAINABLE CHEMISTRY; TIO;

CATALYSTS; FUNCTIONAL GROUPS; GOLD; KETONES; MOLECULES; NITROGEN COMPOUNDS; OLEFINS; PALLADIUM; PLATINUM; TITANIUM DIOXIDE;

HYDROGENATION;

ACRIDINE; ALKENE; AROMATIC COMPOUND; FUNCTIONAL GROUP; GOLD NANOPARTICLE; HALOGEN; HYDROGEN; ISOQUINOLINE; KETONE; LEAD; NITROGEN; PLATINUM; QUINOLINE DERIVATIVE; RUTHENIUM; TITANIUM DIOXIDE;

ARTICLE; BIOTRANSFORMATION; CATALYSIS; CATALYST; CHEMICAL REACTION; HYDROGENATION; PARTICLE SIZE; REACTION TIME; TEMPERATURE;

CATALYSIS; GOLD; HYDROGEN; HYDROGENATION; METAL NANOPARTICLES; MOLECULAR STRUCTURE; QUINOLINES; TITANIUM;

EID: 84867825866     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja3066978     Document Type: Article

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