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Volumn 32, Issue 2, 2003, Pages 180-181

Nanoscale palladium cluster immobilized on a TiO2 surface as an efficient catalyst for liquid-phase wacker oxidation of higher terminal olefins

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE DERIVATIVE; COPPER CHLORIDE; OXYGEN; PALLADIUM; TITANIUM DIOXIDE;

EID: 0037883463     PISSN: 03667022     EISSN: None     Source Type: Journal    
DOI: 10.1246/cl.2003.180     Document Type: Article
Times cited : (35)

References (19)
  • 1
    • 85083243520 scopus 로고    scopus 로고
    • An excellent review of the Wacker oxidation: J. Tsuji, Synthesis, 1984, 369; J. Tsuji, "Palladium Reagents and Catalysts Innovations in Organic Synthesis," John Wiley & Sons, New York (1998).
    • Synthesis , vol.1984 , pp. 369
    • Tsuji, J.1
  • 3
    • 0029989836 scopus 로고    scopus 로고
    • 2: b) A. B. Smith, III, Y. S. Cho, and G. K. Friestad, Tetrahedron Lett., 39, 8765 (1998). Pd-amine complexes: c) G.-J. ten Brink, I. W. C. E. Arends, G. Papadogianakis, and R. A. Sheldon, Chem. Commun., 1998, 2359. d) T. Nishimura, N. Kakiuchi, T. Onoue, K. Ohe, and S. Uemura, J. Chem. Soc., Perkin Trans. 1, 2000, 1915.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 3990
    • Hosokawa, T.1    Takano, M.2    Murahashi, S.-I.3
  • 4
    • 0032569909 scopus 로고    scopus 로고
    • 2: b) A. B. Smith, III, Y. S. Cho, and G. K. Friestad, Tetrahedron Lett., 39, 8765 (1998). Pd-amine complexes: c) G.-J. ten Brink, I. W. C. E. Arends, G. Papadogianakis, and R. A. Sheldon, Chem. Commun., 1998, 2359. d) T. Nishimura, N. Kakiuchi, T. Onoue, K. Ohe, and S. Uemura, J. Chem. Soc., Perkin Trans. 1, 2000, 1915.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 8765
    • Smith A.B. III1    Cho, Y.S.2    Friestad, G.K.3
  • 5
    • 0038643631 scopus 로고    scopus 로고
    • 2: b) A. B. Smith, III, Y. S. Cho, and G. K. Friestad, Tetrahedron Lett., 39, 8765 (1998). Pd-amine complexes: c) G.-J. ten Brink, I. W. C. E. Arends, G. Papadogianakis, and R. A. Sheldon, Chem. Commun., 1998, 2359. d) T. Nishimura, N. Kakiuchi, T. Onoue, K. Ohe, and S. Uemura, J. Chem. Soc., Perkin Trans. 1, 2000, 1915.
    • Chem. Commun. , vol.1998 , pp. 2359
    • Ten Brink, G.-J.1    Arends, I.W.C.E.2    Papadogianakis, G.3    Sheldon, R.A.4
  • 6
    • 0034697701 scopus 로고    scopus 로고
    • 2: b) A. B. Smith, III, Y. S. Cho, and G. K. Friestad, Tetrahedron Lett., 39, 8765 (1998). Pd-amine complexes: c) G.-J. ten Brink, I. W. C. E. Arends, G. Papadogianakis, and R. A. Sheldon, Chem. Commun., 1998, 2359. d) T. Nishimura, N. Kakiuchi, T. Onoue, K. Ohe, and S. Uemura, J. Chem. Soc., Perkin Trans. 1, 2000, 1915.
    • J. Chem. Soc., Perkin Trans. 1 , vol.2000 , pp. 1915
    • Nishimura, T.1    Kakiuchi, N.2    Onoue, T.3    Ohe, K.4    Uemura, S.5
  • 7
    • 0001843455 scopus 로고    scopus 로고
    • A recent review of the vapor-phase Wacker oxidation of light olefins by heterogeneous catalysts: D. E. De Vos, B. F. Sels, and P. A. Jacobs, Adv. Catal., 46, 1 (2001).
    • (2001) Adv. Catal. , vol.46 , pp. 1
    • De Vos, D.E.1    Sels, B.F.2    Jacobs, P.A.3
  • 14
    • 0037629172 scopus 로고    scopus 로고
    • note
    • 2 reference samples.
  • 15
    • 0038643632 scopus 로고    scopus 로고
    • note
    • 2O (0.5 mL), and 1-decene (0.14 g, 1 mmol) was added. Then, the reaction mixture was vigorously stirred at 80°C for 2 h. The catalyst was separated by filtration, and GC analysis of the filtrate showed 88% yield of 2-decanone.
  • 18
    • 0038643633 scopus 로고    scopus 로고
    • note
    • 2O resulted in less than a 1% yield of 2-decanone.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.