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Volumn 13, Issue 19, 2011, Pages 4988-4991

Gold(III)-catalyzed direct acetoxylation of arenes with iodobenzene diacetate

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EID: 80054772245     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol202075x     Document Type: Article
Times cited : (35)

References (51)
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    • For a recent report on AuCl3-catalyzed direct amination of arenes, see
    • For a recent report on AuCl3-catalyzed direct amination of arenes, see: Gu, L.; Neo, B. S.; Zhang, Y. Org. Lett. 2011, 13, 1872.
    • (2011) Org. Lett. , vol.13 , pp. 1872
    • Gu, L.1    Neo, B.S.2    Zhang, Y.3
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    • For a review on hypervalent iodine
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    • Zhdankin, V.V.1    Stang, P.2
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    • For detailed discussion on the acetoxylation and homocoupling, see Supporting Information
    • For detailed discussion on the acetoxylation and homocoupling, see Supporting Information.
  • 44
  • 45
    • 79955510598 scopus 로고    scopus 로고
    • Recently, Zhang and coworkers have observed a normal KIE value of 1.1 in Au(III)-catalyzed aromatic auration
    • Recently, Zhang and coworkers have observed a normal KIE value of 1.1 in Au(III)-catalyzed aromatic auration; see: Zhang, G.; Luo, Y.; Wang, Y.; Zhang, L. Angew. Chem., Int. Ed. 2011, 50, 4450.
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 4450
    • Zhang, G.1    Luo, Y.2    Wang, Y.3    Zhang, L.4
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    • Such a mechanism is possible because it is known that nonsymmetrical aryl-(phenyl) iodonium acetates can be formed from electron-rich arenes under Lewis acidic conditions
    • Lubriks, D.; Sokolovs, I.; Suna, E. Org. Lett. 2011, 13, 4324. Such a mechanism is possible because it is known that nonsymmetrical aryl-(phenyl) iodonium acetates can be formed from electron-rich arenes under Lewis acidic conditions.
    • (2011) Org. Lett. , vol.13 , pp. 4324
    • Lubriks, D.1    Sokolovs, I.2    Suna, E.3
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    • 33748725809 scopus 로고    scopus 로고
    • We thank the referee who called our attention to such mechanistic possibility
    • Shah, A.; Pike, V. W.; Widdowson, D. A. J. Chem. Soc., Perkin Trans. 1 1997, 2463. We thank the referee who called our attention to such mechanistic possibility.
    • (1997) J. Chem. Soc. Perkin Trans. , vol.1 , pp. 2463
    • Shah, A.1    Pike, V.W.2    Widdowson, D.A.3
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    • For a recent report of direct acetoxylation of anilide promoted by stoichiometric BF3 3 OEt2
    • For a recent report of direct acetoxylation of anilide promoted by stoichiometric BF3 3 OEt2, see: Liu, H.; Wang, X.; Gu, Y. Org. Biomol. Chem. 2011, 9, 1614.
    • (2011) Org. Biomol. Chem. , vol.9 , pp. 1614
    • Liu, H.1    Wang, X.2    Gu, Y.3


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