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85083243520
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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).
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Synthesis
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Tsuji, J.1
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0029989836
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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.
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Hosokawa, T.1
Takano, M.2
Murahashi, S.-I.3
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0032569909
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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.
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Tetrahedron Lett.
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Smith A.B. III1
Cho, Y.S.2
Friestad, G.K.3
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0038643631
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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.
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Chem. Commun.
, vol.1998
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Ten Brink, G.-J.1
Arends, I.W.C.E.2
Papadogianakis, G.3
Sheldon, R.A.4
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6
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0034697701
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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.
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J. Chem. Soc., Perkin Trans. 1
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Nishimura, T.1
Kakiuchi, N.2
Onoue, T.3
Ohe, K.4
Uemura, S.5
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7
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0001843455
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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).
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Adv. Catal.
, vol.46
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De Vos, D.E.1
Sels, B.F.2
Jacobs, P.A.3
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8
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0000950320
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3H: c) A. Kishi, T. Higashino, S. Sakaguchi, and Y. Ishii, Tetrahedron Lett., 41, 99 (2000).
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Catal. Lett.
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Arhancet, J.P.1
Davis, M.E.2
Hanson, B.E.3
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0000508104
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3H: c) A. Kishi, T. Higashino, S. Sakaguchi, and Y. Ishii, Tetrahedron Lett., 41, 99 (2000).
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J. Catal.
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Tang, H.G.1
Sherrington, D.C.2
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0033991984
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3H: c) A. Kishi, T. Higashino, S. Sakaguchi, and Y. Ishii, Tetrahedron Lett., 41, 99 (2000).
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Tetrahedron Lett.
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Kishi, A.1
Higashino, T.2
Sakaguchi, S.3
Ishii, Y.4
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11
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0037023077
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a) K. Ebitani, K.-M. Choi, T. Mizugaki, and K. Kaneda, Langmuir, 18, 1849 (2002).
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(2002)
Langmuir
, vol.18
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Ebitani, K.1
Choi, K.-M.2
Mizugaki, T.3
Kaneda, K.4
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12
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0037967449
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in press
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b) K.-M. Choi, T. Akita, T. Mizugaki, K. Ebitani, and K. Kaneda, New J. Chem., in press.
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New J. Chem.
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Choi, K.-M.1
Akita, T.2
Mizugaki, T.3
Ebitani, K.4
Kaneda, K.5
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14
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0037629172
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note
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2 reference samples.
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15
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0038643632
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note
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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.
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17
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0037010004
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b) K. Mori, K. Yamaguchi, T. Hara, T. Mizugaki, K. Ebitani, and K. Kaneda, J. Am. Chem. Soc., 124, 11572 (2002).
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(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 11572
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Mori, K.1
Yamaguchi, K.2
Hara, T.3
Mizugaki, T.4
Ebitani, K.5
Kaneda, K.6
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18
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0038643633
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note
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2O resulted in less than a 1% yield of 2-decanone.
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