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Volumn 10, Issue 21, 2008, Pages 4971-4974

Palladium-catalyzed hiyama cross-coupling reactions of aryl mesylates

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EID: 57749117273     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol802049t     Document Type: Article
Times cited : (75)

References (68)
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  • 17
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    • For examples of Sonogashira coupling, see: (a) Fu, X, Zhang, S, Yin, J, Schumacher, D. P Tetrahedron Lett. 2002, 43, 6673
    • For examples of Sonogashira coupling, see: (a) Fu, X.; Zhang, S.; Yin, J.; Schumacher, D. P Tetrahedron Lett. 2002, 43, 6673.
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    • Kumada coupling: (a) Roy, A. H.; Hartwig, J. F. J. Am. Chem. Soc. 2003, 125, 8704.
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    • Iron-catalyzed coupling of alkyl Grignard reagents with ArOTs
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  • 31
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    • Schio, L.; Chatreaux, F.; Klich, M Tetrahedron Lett. 2000, 41, 1543. Negishi-type reaction of arenesulfonates:
    • (g) Schio, L.; Chatreaux, F.; Klich, M Tetrahedron Lett. 2000, 41, 1543. Negishi-type reaction of arenesulfonates:
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    • Carbonylation reaction
    • (j) Zhang, L.; Wu, J. J. Am. Chem, Soc. 2008, 130, 12250. Carbonylation reaction:
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    • For C-S bond formation (one substrate example), see: (b) Fernández-Rodríguez, M. A.; Shen, Q.; Hartwig, J. F. J. Am. Chem. Soc. 2006, 128, 2180. For Buchwald-Hartwig amidation, see:
    • For C-S bond formation (one substrate example), see: (b) Fernández-Rodríguez, M. A.; Shen, Q.; Hartwig, J. F. J. Am. Chem. Soc. 2006, 128, 2180. For Buchwald-Hartwig amidation, see:
  • 39
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    • Nickel-catalyzed C-C bond couplings of aryl mesylates, see: a
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    • (1996) Tetrahedron Lett , vol.37 , pp. 8531
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    • For direct cross-coupling of 4-mesylcoumarins with aryl- or vinyl halides, see: i
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    • (2004) Synlett , pp. 2364
    • Lei, J.-G.1    Xu, M.-H.2    Lin, G.-Q.3
  • 48
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    • Palladium-catalyzed animation of aryl mesylates: (a) So, C. M.; Zhou, Z.; Lau, C. P.; Kwong, F. Y. Angew. Chem., Int. Ed. 2008, 47, 6402. Palladium-catalyzed carbonylation of aryl mesylates:
    • Palladium-catalyzed animation of aryl mesylates: (a) So, C. M.; Zhou, Z.; Lau, C. P.; Kwong, F. Y. Angew. Chem., Int. Ed. 2008, 47, 6402. Palladium-catalyzed carbonylation of aryl mesylates:
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    • For a review of the Hiyama reaction, see: a, Diederich, F, Stang, P. J, Eds, Wiley-VCH: New York, Chapter 10
    • For a review of the Hiyama reaction, see: (a) Hiyama, T. In Metal-Catalyzed Cross-Coupling Reactions; Diederich, F., Stang, P. J., Eds.; Wiley-VCH: New York, 1998; Chapter 10.
    • (1998) Metal-Catalyzed Cross-Coupling Reactions
    • Hiyama, T.1
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    • For some recent developments in Hiyama cross-coupling chemistry, see: a
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    • (2002) Acc. Chem. Res , vol.35 , pp. 835
    • Denmark, S.E.1    Sweis, R.F.2
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    • references therein, DOI: 10.1021/ar800036s and
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    • For a recent review on the development and application of bulky electron-rich phosphines for palladium-catalyzed cross-coupling reaction of aryl halides and sulfonates, see: Zapf, A, Beller, M. Chem. Commun. 2005, 431, and references cited therein
    • For a recent review on the development and application of bulky electron-rich phosphines for palladium-catalyzed cross-coupling reaction of aryl halides and sulfonates, see: Zapf, A.; Beller, M. Chem. Commun. 2005, 431, and references cited therein.


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