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Volumn 132, Issue 24, 2010, Pages 8270-8272

PyDipSi: A general and easily modifiable/traceless Si-tethered directing group for C-H acyloxylation of arenes

Author keywords

[No Author keywords available]

Indexed keywords

HALOARENES; PYRIDYL; REGIO-SELECTIVE;

EID: 77953624806     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja1033167     Document Type: Article
Times cited : (173)

References (61)
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    • For early examples of Pd-catalyzed C-H acetoxylation of arenes, see
    • For early examples of Pd-catalyzed C-H acetoxylation of arenes, see: Henry, P. M. J. Org. Chem. 1971, 36, 1886
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    • For recent representative examples of Pd-catalyzed C-H acetoxylation of arenes, see
    • For recent representative examples of Pd-catalyzed C-H acetoxylation of arenes, see: Dick, A. R., Hull, K. L., and Sanford, M. S. J. Am. Chem. Soc. 2004, 126, 2300
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    • For a recent review of transition-metal-catalyzed syntheses of hydroxylated arenes, see
    • For a recent review of transition-metal-catalyzed syntheses of hydroxylated arenes, see: Alonso, D. A., Nájera, C., Pastor, I. M., and Yus, M. Chem. - Eur. J. 2010, 16, 5274
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    • For employment of the pyridyldimethylsilyl directing group in Heck arylations, see
    • For employment of the pyridyldimethylsilyl directing group in Heck arylations, see: Itami, K., Mitsudo, K., Kamei, T., Koike, T., Nokami, T., and Yoshida, J.-I. J. Am. Chem. Soc. 2000, 122, 12013
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    • For employment of the dimethylhydrosilyl directing group in Ir-catalyzed C-H borylations, see
    • For employment of the dimethylhydrosilyl directing group in Ir-catalyzed C-H borylations, see: Robbins, D. W., Boebel, T. A., and Hartwig, J. F. J. Am. Chem. Soc. 2010, 132, 4068
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    • 2 species
    • 2 species.
  • 32
    • 55549111900 scopus 로고    scopus 로고
    • For a recent example of an acetate cross-coupling reaction, see
    • For a recent example of an acetate cross-coupling reaction, see: Guan, B.-T., Wang, Y., Li, B.-J., Yu, D.-G., and Shi, Z.-J. J. Am. Chem. Soc. 2008, 130, 14468
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 14468
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    • See the Supporting Information for details
    • See the Supporting Information for details.
  • 39
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    • For another recent example of the formation of palladacycles in C-H activation processes, see
    • For another recent example of the formation of palladacycles in C-H activation processes, see: Giri, R., Lam, J. K., and Yu, J.-Q. J. Am. Chem. Soc. 2009, 132, 686
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    • Presumably, this reaction proceeds via formation of a palladacycle. See the Supporting Information for details
    • Presumably, this reaction proceeds via formation of a palladacycle. See the Supporting Information for details.
  • 45
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    • For an example of ortho hydroxylation of haloarenes, see
    • For an example of ortho hydroxylation of haloarenes, see: de Rege, F. M. G. and Buchwald, S. L. Tetrahedron 1995, 51, 4291
    • (1995) Tetrahedron , vol.51 , pp. 4291
    • De Rege, F.M.G.1    Buchwald, S.L.2
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.