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Volumn 132, Issue 40, 2010, Pages 14076-14078

Palladium-catalyzed conversion of aryl and vinyl triflates to bromides and chlorides

Author keywords

[No Author keywords available]

Indexed keywords

PALLADIUM-CATALYZED CONVERSION; PHOSPHINE LIGANDS; TRIFLATES; VINYL HALIDES;

EID: 77957721302     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja107481a     Document Type: Article
Times cited : (94)

References (43)
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    • For a selected review, see
    • For a selected review, see: Ritter, K. Synthesis 1993, 735
    • (1993) Synthesis , pp. 735
    • Ritter, K.1
  • 13
    • 48749097381 scopus 로고    scopus 로고
    • For general reviews on metal-mediated carbon-halogen bond formation, see
    • For general reviews on metal-mediated carbon-halogen bond formation, see: Vigalok, A. Chem.-Eur. J. 2008, 14, 5102
    • (2008) Chem.-Eur. J. , vol.14 , pp. 5102
    • Vigalok, A.1
  • 25
    • 77955828687 scopus 로고    scopus 로고
    • An example of reversible oxidative addition of palladium into 2-bromoindoles has appeared
    • An example of reversible oxidative addition of palladium into 2-bromoindoles has appeared: Newman, S. G. and Lautens, M. J. Am. Chem. Soc. 2010, 132, 11416
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 11416
    • Newman, S.G.1    Lautens, M.2
  • 31
    • 0036215037 scopus 로고    scopus 로고
    • For the Ni-catalyzed conversion of pyranyl triflates to pyranyl bromides, see:, For the Ru-catalyzed conversion of alkenyl triflates to alkenyl halides, see:, Chem. Commun. 2009, 5088
    • For the Ni-catalyzed conversion of pyranyl triflates to pyranyl bromides, see: Milne, J. E., Jarowicki, K., and Kocienski, P. J. Synlett 2002, 607 For the Ru-catalyzed conversion of alkenyl triflates to alkenyl halides, see: Shirakawa, E., Imazaki, Y., and Hayashi, T. Chem. Commun. 2009, 5088
    • (2002) Synlett , pp. 607
    • Milne, J.E.1    Jarowicki, K.2    Kocienski, P.J.3    Shirakawa, E.4    Imazaki, Y.5    Hayashi, T.6
  • 41
    • 0000471742 scopus 로고
    • For examples of Pd-catalyzed cross-coupling of organoaluminum reagents, see
    • For examples of Pd-catalyzed cross-coupling of organoaluminum reagents, see: Babu, S. and Negishi, E. J. Am. Chem. Soc. 1976, 98, 6729
    • (1976) J. Am. Chem. Soc. , vol.98 , pp. 6729
    • Babu, S.1    Negishi, E.2
  • 43
    • 77957714026 scopus 로고    scopus 로고
    • About 5% of 1- n -butyl-4-iodobenzene was formed when 4- n -butylphenyl triflate was subjected to similar catalytic conditions using KI as the iodide source
    • About 5% of 1- n -butyl-4-iodobenzene was formed when 4- n -butylphenyl triflate was subjected to similar catalytic conditions using KI as the iodide source.


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