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Volumn 346, Issue 13-15, 2004, Pages 1812-1817

Use of "homeopathic" ligand-free palladium as catalyst for aryl-aryl coupling reactions

Author keywords

Biaryls; Cross coupling; Ligand free palladium; Nanoclusters; Negishi reaction; Suzuki reaction

Indexed keywords

BROMINE DERIVATIVE; HALIDE; PALLADIUM;

EID: 12344337312     PISSN: 16154150     EISSN: None     Source Type: Journal    
DOI: 10.1002/adsc.200404210     Document Type: Article
Times cited : (197)

References (47)
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    • For reviews, see: a) N. Miyaura, A. Suzuki, Chem. Rev. 1995, 95, 2457; b) A. Suzuki, J. Organomet. Chem. 1999, 576, 147; c) A. Suzuki, in: Metal-Catalyzed Cross-coupling Reactions, (Eds.: F. Diederich, P. J. Stang), Wiley-VCH, Weinheim, 1998, p. 49.
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    • (1998) Metal-Catalyzed Cross-coupling Reactions , pp. 49
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    • For some reviews and leading references on Pd/phosphine catalysts and palladacycles as catalyst for the Suzuki reaction on aryl chlorides, see: a) A. F. Littke, G. Fu, Angew. Chem. Int. Ed. 2002, 41, 4176; b) R. B. Bedford, Chem. Commun. 2003, 1787; c) M. Miura, Angew. Chem. Int. Ed. 2004, 43, 2201; d) L. Botella, C. Nájera, Angew. Chem. Int. Ed. 2002, 41, 179.
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 4176
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    • For some reviews and leading references on Pd/phosphine catalysts and palladacycles as catalyst for the Suzuki reaction on aryl chlorides, see: a) A. F. Littke, G. Fu, Angew. Chem. Int. Ed. 2002, 41, 4176; b) R. B. Bedford, Chem. Commun. 2003, 1787; c) M. Miura, Angew. Chem. Int. Ed. 2004, 43, 2201; d) L. Botella, C. Nájera, Angew. Chem. Int. Ed. 2002, 41, 179.
    • (2003) Chem. Commun. , pp. 1787
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  • 34
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    • For some reviews and leading references on Pd/phosphine catalysts and palladacycles as catalyst for the Suzuki reaction on aryl chlorides, see: a) A. F. Littke, G. Fu, Angew. Chem. Int. Ed. 2002, 41, 4176; b) R. B. Bedford, Chem. Commun. 2003, 1787; c) M. Miura, Angew. Chem. Int. Ed. 2004, 43, 2201; d) L. Botella, C. Nájera, Angew. Chem. Int. Ed. 2002, 41, 179.
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 2201
    • Miura, M.1
  • 35
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    • For some reviews and leading references on Pd/phosphine catalysts and palladacycles as catalyst for the Suzuki reaction on aryl chlorides, see: a) A. F. Littke, G. Fu, Angew. Chem. Int. Ed. 2002, 41, 4176; b) R. B. Bedford, Chem. Commun. 2003, 1787; c) M. Miura, Angew. Chem. Int. Ed. 2004, 43, 2201; d) L. Botella, C. Nájera, Angew. Chem. Int. Ed. 2002, 41, 179.
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 179
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    • note
    • The presence of large excess of water leads to the formation of unidentified high-boiling point impurities, especially after prolonged reaction times.
  • 40
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    • For an example of microwave-assisted transition metal-free Suzuki-type coupling of aryl bromides, see: N. E. Leadbeater, M. Marco, J. Org. Chem. 2003, 68, 5660.
    • (2003) J. Org. Chem. , vol.68 , pp. 5660
    • Leadbeater, N.E.1    Marco, M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.