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Volumn 5, Issue 11, 2010, Pages 2336-2340

Highly effective Pd-catalyzed ortho olefination of acetanilides: Broad substrate scope and high tolerability

Author keywords

acetanilides; C H activation; olefination; palladium

Indexed keywords

ACETANILIDES; C-H ACTIVATION; FUNCTIONALIZED; OLEFINATION; STERIC PROPERTIES;

EID: 78349253455     PISSN: 18614728     EISSN: 1861471X     Source Type: Journal    
DOI: 10.1002/asia.201000613     Document Type: Article
Times cited : (58)

References (64)
  • 2
  • 3
  • 21
    • 4444264948 scopus 로고
    • For reviews on the Mizoroki-Heck reaction, see
    • For reviews on the Mizoroki-Heck reaction, see, R. F. Heck, Acc. Chem. Res. 1979, 12, 146-151
    • (1979) Acc. Chem. Res. , vol.12 , pp. 146-151
    • Heck, R.F.1
  • 24
    • 22744442306 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 4442-4489.
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 4442-4489
  • 29
    • 67649488045 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 5094-5115
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 5094-5115
  • 35
    • 0011416015 scopus 로고
    • For examples of the Pd-catalyzed Fujiwara-Moritani reaction using acetanilide as a directing group, see H. Horino, N. Inoue, Tetrahedron Lett. 1979, 20, 2403-2406
    • (1979) Tetrahedron Lett. , vol.20 , pp. 2403-2406
    • Horino, H.1    Inoue, N.2
  • 42
    • 77951873890 scopus 로고    scopus 로고
    • During the preparation of this manuscript, the Rh-catalyzed olefination of acetanilides has been reported; see
    • T. Nishikata, B. H. Lipshutz, Org. Lett. 2010, 12, 1972-1975. During the preparation of this manuscript, the Rh-catalyzed olefination of acetanilides has been reported; see
    • (2010) Org. Lett. , vol.12 , pp. 1972-1975
    • Nishikata, T.1    Lipshutz, B.H.2
  • 46
    • 27144450136 scopus 로고    scopus 로고
    • For examples of Pd-catalyzed reaction of 2-arylaniline derivatives involving C-H activation at the C2' position, see
    • For examples of Pd-catalyzed reaction of 2-arylaniline derivatives involving C-H activation at the C2' position, see, W. C. P. Tsang, N. Zheng, S. L. Buchwald, J. Am. Chem. Soc. 2005, 127, 14560-14561
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 14560-14561
    • Tsang, W.C.P.1    Zheng, N.2    Buchwald, S.L.3
  • 49
    • 38849126856 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 1115-1118
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 1115-1118
  • 51
    • 69549090264 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 6892-6895
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 6892-6895
  • 54
    • 78349266716 scopus 로고    scopus 로고
    • For Pd-catalyzed Fujiwara-Moritani reaction at room temperature, see: references [7c-d], [7h], and [8b]
    • For Pd-catalyzed Fujiwara-Moritani reaction at room temperature, see: references [7c-d], [7h], and [8b].
  • 55
    • 78349235277 scopus 로고    scopus 로고
    • CCDC 779517 (2p) and CCDC 779518 (I) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • CCDC 779517 (2p) and CCDC 779518 (I) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via.
  • 58
    • 77949792138 scopus 로고    scopus 로고
    • For a review, see
    • For a review, see, K. Muñz, Angew. Chem. 2009, 121, 9576-9588
    • (2009) Angew. Chem. , vol.121 , pp. 9576-9588
    • Muñz, K.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.