메뉴 건너뛰기




Volumn 135, Issue 44, 2013, Pages 16288-16291

Nickel/bis(oxazoline)-catalyzed asymmetric negishi arylations of racemic secondary benzylic electrophiles to generate enantioenriched 1,1-diarylalkanes

Author keywords

[No Author keywords available]

Indexed keywords

ARYL SUBSTITUENTS; ARYLZINC REAGENTS; BENZYLIC ALCOHOLS; BIOACTIVE COMPOUNDS; GRAM-SCALE SYNTHESIS; MILD REACTION CONDITIONS; NEGISHI CROSS-COUPLING; STEREOGENIC CENTERS;

EID: 84887750453     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja408561b     Document Type: Article
Times cited : (171)

References (26)
  • 3
    • 84884746772 scopus 로고    scopus 로고
    • Feldman, D. Pike, J. W. Adams, J. S. Elsevier: London
    • Stayrook, K. R.; Carson, M. W.; Ma, Y. L.; Dodge, J. A. In Vitamin D; Feldman, D.; Pike, J. W.; Adams, J. S., Eds.; Elsevier: London, 2011; pp 1497-1508.
    • (2011) Vitamin D , pp. 1497-1508
    • Stayrook, K.R.1    Carson, M.W.2    Ma, Y.L.3    Dodge, J.A.4
  • 15
    • 84856021728 scopus 로고    scopus 로고
    • For a recent application in a total synthesis of a natural product (carolacton), see: Schmidt, T.; Kirschning, A. Angew. Chem., Int. Ed. 2012, 51, 1063
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 1063
    • Schmidt, T.1    Kirschning, A.2
  • 23
    • 84887698603 scopus 로고    scopus 로고
    • Refs 6b and 6d.
    • Refs 6b and 6d.
  • 24
    • 84871242844 scopus 로고    scopus 로고
    • For leading references to nickel-catalyzed cross-coupling reactions of aryl electrophiles, including processes that involve C-O bond cleavage: Yamaguchi, J.; Muto, K.; Itami, K. Eur. J. Org. Chem. 2013, 19
    • (2013) Eur. J. Org. Chem. , pp. 19
    • Yamaguchi, J.1    Muto, K.2    Itami, K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.