Palladium-catalyzed peripheral arylation of 5-pyrazolones via enolizable bond protection

Synthesis

Volumn , Issue 11, 2011, Pages 1783-1791

  Bin, Hye Rin ^a,b   Bae, Yun Soo ^c   Kim, Guncheol ^b   Lee, Kee In ^a  

^a Korea Research Institute of Chemical Technology   (South Korea)

^b Chungnam National University   (South Korea)

^c Ewha Womans University   (South Korea)

Author keywords

arylpyrazole; peripheral arylation; pyrazolone; Suzuki Miyaura; tautomers

Indexed keywords

ARYLPYRAZOLE; PERIPHERAL ARYLATION; PYRAZOLONE; SUZUKI-MIYAURA; TAUTOMERS;

AROMATIC COMPOUNDS; SCAFFOLDS;

CHEMICAL REACTIONS;

2 PYRAZOLIN 5 ONE; 5 HYDROXY 3 BIPHENYLPYRAZOLE DERIVATIVE; BORONIC ACID DERIVATIVE; HYDROXYL GROUP; MOLECULAR SCAFFOLD; PALLADIUM; PALLADIUM DICHLORIDE; PYRAZOLE DERIVATIVE; PYRAZOLONE DERIVATIVE; TERPHENYLPYRAZOLE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; ARYLATION; CATALYSIS; CHEMICAL BOND; CHEMICAL STRUCTURE; CROSS COUPLING REACTION; SUZUKI REACTION;

EID: 79956366442     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0030-1260018     Document Type: Article

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