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Volumn 13, Issue 20, 2007, Pages 5937-5943

Heterogeneous Pd/C-catalyzed ligand-free, room-temperature suzuki-miyaura coupling reactions in aqueous media

Author keywords

Aryl halides; C C coupling; Heterogeneous catalysis; Palladium

Indexed keywords

CATALYSIS; COUPLING AGENTS; DERIVATIVES; HALOGEN ELEMENTS; PALLADIUM COMPOUNDS; THERMAL EFFECTS;

EID: 34547230604     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200601795     Document Type: Article
Times cited : (242)

References (58)
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    • Many of supported palladium catalysts for the Suzuki-Miyaura coupling reaction have been reported; for selected recent reports, see: a Q. Yang, S. Ma, J. Li, F. Xiao, H. Xiong, Chem. Commun. 2006, 2495-2497;
    • Many of supported palladium catalysts for the Suzuki-Miyaura coupling reaction have been reported; for selected recent reports, see: a) Q. Yang, S. Ma, J. Li, F. Xiao, H. Xiong, Chem. Commun. 2006, 2495-2497;
  • 26
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    • For a review of the Pd/C catalyzed Suzuki-Miyaura coupling reaction, see: F.-X. Felpin, T. Ayad, S. Mitra, Eur. J. Org. Chem. 2006, 2679-2690.
    • For a review of the Pd/C catalyzed Suzuki-Miyaura coupling reaction, see: F.-X. Felpin, T. Ayad, S. Mitra, Eur. J. Org. Chem. 2006, 2679-2690.
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    • K type wet-type Pd/C from N. E. Chemcat was used unless otherwise noted
    • K type wet-type Pd/C from N. E. Chemcat was used unless otherwise noted.
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    • 4]-catalyzed Suzuki-Miyaura coupling reaction; see ref. [2d].
    • 4]-catalyzed Suzuki-Miyaura coupling reaction; see ref. [2d].
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    • T. Ikawa, H. Sajiki, K. Hirota, Tetrahedron 2004, 60, 6189-6195; Lysén and Köhler also reported that differences in the catalytic activity of Pd/C in the Suzuki-Miyaura coupling reaction can depend on the supplier, see ref. [8a].
    • T. Ikawa, H. Sajiki, K. Hirota, Tetrahedron 2004, 60, 6189-6195; Lysén and Köhler also reported that differences in the catalytic activity of Pd/C in the Suzuki-Miyaura coupling reaction can depend on the supplier, see ref. [8a].
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    • The homocoupling reaction of aryl boronic acids in Pd-catalyzed Suzuki-Miyaura cross-coupling reactions is known to proceed; for a recent report, see: C. Adamo, C. Amatore, I. Ciofini, A. Jutand, H. Lakmini, J. Am. Chem. Soc. 2006, 125, 6829-6936, and references cited in reference [2d
    • The homocoupling reaction of aryl boronic acids in Pd-catalyzed Suzuki-Miyaura cross-coupling reactions is known to proceed; for a recent report, see: C. Adamo, C. Amatore, I. Ciofini, A. Jutand, H. Lakmini, J. Am. Chem. Soc. 2006, 125, 6829-6936, and references cited in reference [2d].
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    • A large degree of homocoupling reactions of aryl boronic acids result from exposure to air in the presence of aqueous base; see ref, 2d
    • A large degree of homocoupling reactions of aryl boronic acids result from exposure to air in the presence of aqueous base; see ref. [2d].
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    • The residual palladium was assayed using Shimadzu ICP8000 (Shimadzu, Kyoto, Japan).
    • The residual palladium was assayed using Shimadzu ICP8000 (Shimadzu, Kyoto, Japan).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.