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Volumn 16, Issue 14, 2010, Pages 4279-4283

An efficient low-temperature stille-migita cross-coupling reaction for heteroaromatic compounds by Pd-PEPPSI-IPent

Author keywords

Biaryls; Cross coupling; Heterocycles; Palladium; Stille migita reaction

Indexed keywords

BIARYLS; CARBON-CARBON BOND; CROSS COUPLING REACTIONS; CROSS-COUPLINGS; HETEROAROMATIC COMPOUNDS; HETEROCYCLES PALLADIUM; HIGH EFFICIENCY; LOW TEMPERATURES; ORGANOSTANNANES; PD CATALYST; PRECATALYSTS;

EID: 77950792028     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200903337     Document Type: Article
Times cited : (87)

References (50)
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    • For cases in which moderate product conversions were obtained (i.e., ≈75%), the major impurity in the crude mixture was unreacted starting material (i.e., ArX) and allowing these reactions to proceed longer resulted in greater than 90 % conversions on an individual basis.
    • For cases in which moderate product conversions were obtained (i.e., ≈75%), the major impurity in the crude mixture was unreacted starting material (i.e., ArX) and allowing these reactions to proceed longer resulted in greater than 90 % conversions on an individual basis.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.