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Volumn 132, Issue 14, 2010, Pages 4978-4979

Cationic palladium(II) catalysis: C-H activation/suzuki-miyaura couplings at room temperature

Author keywords

[No Author keywords available]

Indexed keywords

ARYLBORONIC ACIDS; C-H ACTIVATION; CATIONIC PALLADIUM; ELECTROPHILIC SUBSTITUTIONS; ROOM TEMPERATURE;

EID: 77950806013     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja910973a     Document Type: Article
Times cited : (257)

References (50)
  • 39
    • 74549148904 scopus 로고    scopus 로고
    • Fine tunings of ligands generally enhance ease of C-H activations; see
    • Fine tunings of ligands generally enhance ease of C-H activations; see: Wang, D.-H., Engle, K. M., Shi, B.-F., and Yu, J.-Q. Science 2010, 327, 315
    • (2010) Science , vol.327 , pp. 315
    • Wang, D.-H.1    Engle, K.M.2    Shi, B.-F.3    Yu, J.-Q.4
  • 42
    • 74949097467 scopus 로고    scopus 로고
    • A primary isotope effect for a corresponding substituted ortho- benzoate derivative has recently been described, suggesting that intramolecular H-atom abstraction is the rate-determining step; see
    • A primary isotope effect for a corresponding substituted ortho- benzoate derivative has recently been described, suggesting that intramolecular H-atom abstraction is the rate-determining step; see: Xiao, B., Fu, Y., Xu, J., Gong, T.-J., Dai, J.-J., Yi, J., and Liu, L. J. Am. Chem. Soc. 2010, 132, 468
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 468
    • Xiao, B.1    Fu, Y.2    Xu, J.3    Gong, T.-J.4    Dai, J.-J.5    Yi, J.6    Liu, L.7
  • 49
    • 77950809546 scopus 로고    scopus 로고
    • Neither the corresponding acetamides or trifluroacetamide analogues led to arylated products in useful yields (low conversions)
    • Neither the corresponding acetamides or trifluroacetamide analogues led to arylated products in useful yields (low conversions).
  • 50
    • 77950849369 scopus 로고    scopus 로고
    • 2, no reaction takes place
    • 2, no reaction takes place.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.