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Volumn 19, Issue 10, 2013, Pages 3504-3511

Selective arylation and vinylation at the α position of vinylarenes

Author keywords

Heck reaction; olefin insertion; palladium; phosphanes; regioselectivity; styrene

Indexed keywords

ARYLATIONS; FERROCENES; GENERAL METHOD; HECK REACTIONS; INTERMOLECULAR HECK REACTION; MECHANISTIC STUDIES; NAPHTHYL GROUPS; PHOSPHANES; PHOSPHORUS ATOM; STERIC EFFECT; TRIFLATES; VINYL GROUP; VINYLARENES; VINYLATION;

EID: 84874437296     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201203646     Document Type: Article
Times cited : (44)

References (53)
  • 8
    • 84873824359 scopus 로고    scopus 로고
    • Focus on Regioselectivity and Product Outcome in Organic Synthesis
    • (Ed.: M. Oestreich), Wiley, New York
    • P. Nilsson, K. Olofsson, M. Larhed, "Focus on Regioselectivity and Product Outcome in Organic Synthesis" in The Mizoroki-Heck Reaction (Ed.: M. Oestreich), Wiley, New York, 2009, pp. 133.
    • (2009) The Mizoroki-Heck Reaction , pp. 133
    • Nilsson, P.1    Olofsson, K.2    Larhed, M.3
  • 20
    • 80052450415 scopus 로고    scopus 로고
    • review on oxidative Heck reactions:, Y. Su, N. Jiao, Curr. Org. Chem. 2011, 15, 3362
    • (2011) Curr. Org. Chem. , vol.15 , pp. 3362
    • Su, Y.1    Jiao, N.2
  • 21
    • 79952677383 scopus 로고    scopus 로고
    • review on dehydrogenative Heck reactions:, J. Le Bras, J. Muzart, Chem. Rev. 2011, 111, 1170.
    • (2011) Chem. Rev. , vol.111 , pp. 1170
    • Le Bras, J.1    Muzart, J.2
  • 26
    • 78649290549 scopus 로고    scopus 로고
    • A selectivity of 9:1 that favors internal insertion was reported for a special pair of substrates, but for other substrates the selectivity was much lower:, J. Ruan, J. A. Iggo, N. G. Berry, J. Xiao, J. Am. Chem. Soc. 2010, 132, 16689.
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 16689
    • Ruan, J.1    Iggo, J.A.2    Berry, N.G.3    Xiao, J.4
  • 42
    • 84874424205 scopus 로고    scopus 로고
    • We have used a Pd/dnpf catalyst in a selective Heck reaction of aliphatic olefins:, L. Qin, X. Ren, Y. Lu, Y. Li, J. Zhou, Angew. Chem. 2012, 124, 6017
    • (2012) Angew. Chem. , vol.124 , pp. 6017
    • Qin, L.1    Ren, X.2    Lu, Y.3    Li, Y.4    Zhou, J.5
  • 50
    • 84874446579 scopus 로고    scopus 로고
    • CCDC-873139 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.