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Volumn 78, Issue 17, 2013, Pages 8859-8864

Minimizing the amount of nitromethane in palladium-catalyzed cross-coupling with aryl halides

Author keywords

[No Author keywords available]

Indexed keywords

ARYL HALIDES; HETEROCYCLES; HIGH YIELD; LOW TEMPERATURES; NITROMETHANE; PALLADIUM-CATALYZED CROSS-COUPLINGS; TRIFLATES;

EID: 84883758717     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo401249y     Document Type: Article
Times cited : (37)

References (33)
  • 14
    • 0037059437 scopus 로고    scopus 로고
    • For coupling of primary nitroalkanes with aryl halides, see: Vogl, E. M.; Buchwald, S. L. J. Org. Chem. 2002, 67, 106-111
    • (2002) J. Org. Chem. , vol.67 , pp. 106-111
    • Vogl, E.M.1    Buchwald, S.L.2
  • 28
    • 5144228478 scopus 로고    scopus 로고
    • Per ref 20, aryl iodides couple successfully when using nitromethane as the solvent. The results here are consistent with prior work with aryl iodides when oxidative addition is not rate-determining: Wolfe, J. P.; Buchwald, S. L. J. Org. Chem. 1996, 61, 1133-1135
    • (1996) J. Org. Chem. , vol.61 , pp. 1133-1135
    • Wolfe, J.P.1    Buchwald, S.L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.