A phosphine-free heterogeneous Suzuki-Miyaura reaction of aryl bromides catalyzed by MCM-41-supported tridentate nitrogen palladium complex under air

Applied Organometallic Chemistry

Volumn 25, Issue 12, 2011, Pages 871-875

  Zhao, Hong ^a   Ding, Guodong ^b   Xu, Li ^a   Cai, Mingzhong ^b  

^a GUANGDONG PHARMACEUTICAL UNIVERSITY   (China)

^b JIANGXI NORMAL UNIVERSITY   (China)

Author keywords

C C coupling reaction; functionalized MCM 41; heterogeneous catalysis; supported catalyst; tridentate nitrogen palladium complex

Indexed keywords

ARYL BROMIDES; C-C COUPLING REACTIONS; COUPLING PRODUCT; FUNCTIONALIZED; PALLADIUM COMPLEXES; PHOSPHINE-FREE; PYRIDINE-2-CARBOXALDEHYDE; SUZUKI-MIYAURA COUPLING REACTION; SUZUKI-MIYAURA REACTION; TRIDENTATE NITROGEN PALLADIUM COMPLEX; TWO-POINT;

BROMINE COMPOUNDS; CATALYSIS; CATALYST ACTIVITY; CATALYST SUPPORTS; METAL HALIDES; NITROGEN; PHOSPHORUS COMPOUNDS; SYNTHESIS (CHEMICAL);

PALLADIUM COMPOUNDS;

EID: 84655175082     PISSN: 02682605     EISSN: 10990739     Source Type: Journal    
DOI: 10.1002/aoc.1854     Document Type: Article

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