-
1
-
-
0003445429
-
-
Springer: Berlin
-
Comprehensive Asymmetric Catalysis; Jacobsen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer: Berlin, 1999.
-
(1999)
Comprehensive Asymmetric Catalysis
-
-
Jacobsen, E.N.1
Pfaltz, A.2
Yamamoto, H.3
-
12
-
-
0000687963
-
-
Y. Uozumi, K. Kitayama, T. Hyashi, K. Yanagi, and E. Fukuyo Bull. Chem. Soc. Jpn. 68 1995 713
-
(1995)
Bull. Chem. Soc. Jpn.
, vol.68
, pp. 713
-
-
Uozumi, Y.1
Kitayama, K.2
Hyashi, T.3
Yanagi, K.4
Fukuyo, E.5
-
14
-
-
0034344687
-
-
T. Hayashi, S. Hirate, K. Kitayama, H. Tsuji, A. Torii, and Y. Uozumi Chem. Lett. 2000 1272
-
(2000)
Chem. Lett.
, pp. 1272
-
-
Hayashi, T.1
Hirate, S.2
Kitayama, K.3
Tsuji, H.4
Torii, A.5
Uozumi, Y.6
-
15
-
-
0001254371
-
-
T. Hayashi, J.W. Han, A. Takeda, J. Tang, K. Nohmi, K. Mukaide, H. Tsuji, and Y. Uozumi Adv. Synth. Catal. 343 2001 279 See also Ref. 3a
-
(2001)
Adv. Synth. Catal.
, vol.343
, pp. 279
-
-
Hayashi, T.1
Han, J.W.2
Takeda, A.3
Tang, J.4
Nohmi, K.5
Mukaide, K.6
Tsuji, H.7
Uozumi, Y.8
-
16
-
-
0001177322
-
-
For typical examples (asymmetric π-allylic substitution), see: (a) T. Hayashi, H. Iwamura, M. Naito, Y. Matsumoto, Y. Uozumi, M. Miki, and K. Yanagi J. Am. Chem. Soc. 116 1994 775
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 775
-
-
Hayashi, T.1
Iwamura, H.2
Naito, M.3
Matsumoto, Y.4
Uozumi, Y.5
Miki, M.6
Yanagi, K.7
-
18
-
-
0028272046
-
-
T. Hayashi, H. Iwamura, Y. Uozumi, Y. Matsumoto, and F. Ozawa Synthesis 1994 526
-
(1994)
Synthesis
, pp. 526
-
-
Hayashi, T.1
Iwamura, H.2
Uozumi, Y.3
Matsumoto, Y.4
Ozawa, F.5
-
20
-
-
0001916342
-
-
T. Hayashi, M. Kawatsura, H. Iwamura, Y. Yamaura, and Y. Uozumi Chem. Commun. 1996 1767
-
(1996)
Chem. Commun.
, pp. 1767
-
-
Hayashi, T.1
Kawatsura, M.2
Iwamura, H.3
Yamaura, Y.4
Uozumi, Y.5
-
24
-
-
0032557607
-
-
For examples of C1-symmetric binaphthyl-based chiral catalysts, see: (a) M. Ogasawara, K. Yoshida, H. Kamei, K. Kato, U. Yasuhiro, and T. Hayashi Tetrahedron: Asymmetry 9 1998 1779
-
(1998)
Tetrahedron: Asymmetry
, vol.9
, pp. 1779
-
-
Ogasawara, M.1
Yoshida, K.2
Kamei, H.3
Kato, K.4
Yasuhiro, U.5
Hayashi, T.6
-
32
-
-
20844433475
-
-
S.V. Ley, I.R. Baxendale, R.N. Bream, P.S. Jackson, A.G. Leach, D.A. Longbottom, M. Nesi, J.S. Scott, R.I. Storer, and S.J. Taylor J. Chem. Soc., Perkin Trans. 1 2000 3815
-
(2000)
J. Chem. Soc., Perkin Trans. 1
, pp. 3815
-
-
Ley, S.V.1
Baxendale, I.R.2
Bream, R.N.3
Jackson, P.S.4
Leach, A.G.5
Longbottom, D.A.6
Nesi, M.7
Scott, J.S.8
Storer, R.I.9
Taylor, S.J.10
-
35
-
-
0030922520
-
-
For studies on polymer-supported palladium catalysts reported by the author's group, see: (a) Y. Uozumi, H. Danjo, and T. Hayashi Tetrahedron Lett. 38 1997 3557 (π-allylic substitution)
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 3557
-
-
Uozumi, Y.1
Danjo, H.2
Hayashi, T.3
-
37
-
-
0033617433
-
-
(cross-coupling).
-
(c) Uozumi, Y.; Danjo, H.; Hayashi, T. J. Org. Chem. 1999, 64, 3384 (cross-coupling).
-
(1999)
J. Org. Chem.
, vol.64
, pp. 3384
-
-
Uozumi, Y.1
Danjo, H.2
Hayashi, T.3
-
42
-
-
0003492617
-
-
Wiley-VCH: Weinheim and references cited therein
-
For recent reviews on heterogeneous asymmetric catalysis, see (a) Chiral Catalyst Immobilization and Recycling; De Vos, D. E., Vankelecom, I. F. J., Jacobs, P. A., Eds.; Wiley-VCH: Weinheim, 2000, and references cited therein. (b) Doerwald, F. Z. Organic Synthesis on Solid Phase; Wiley-VCH: Weinheim, 2000.
-
(2000)
Chiral Catalyst Immobilization and Recycling
-
-
De Vos, D.E.1
Vankelecom, I.F.J.2
Jacobs, P.A.3
-
43
-
-
0003994252
-
-
Wiley-VCH: Weinheim
-
For recent reviews on heterogeneous asymmetric catalysis, see (a) Chiral Catalyst Immobilization and Recycling; De Vos, D. E., Vankelecom, I. F. J., Jacobs, P. A., Eds.; Wiley-VCH: Weinheim, 2000, and references cited therein. (b) Doerwald, F. Z. Organic Synthesis on Solid Phase; Wiley-VCH: Weinheim, 2000.
-
(2000)
Organic Synthesis on Solid Phase
-
-
Doerwald, F.Z.1
-
45
-
-
0034801528
-
-
For studies on PS-PEG resin-supported chiral palladium catalysts reported by the author's group, see: (a) Y. Uozumi, and K. Shibatomi J. Am. Chem. Soc. 123 2001 2919
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 2919
-
-
Uozumi, Y.1
Shibatomi, K.2
-
47
-
-
0029051258
-
-
For examples of polymeric chiral palladium catalysts, see: (a) P. Gamez, B. Dunjic, F. Fache, and M. Lemaire Tetrahedron: Asymmetry 6 1995 1109
-
(1995)
Tetrahedron: Asymmetry
, vol.6
, pp. 1109
-
-
Gamez, P.1
Dunjic, B.2
Fache, F.3
Lemaire, M.4
-
51
-
-
0037131591
-
-
C.E. Song, J.W. Yang, Y.E. Roh, S.-G. Lee, J.H. Ahn, and H. Han Angew. Chem., Int. Ed. Engl. 4 2002 3852
-
(2002)
Angew. Chem., Int. Ed. Engl.
, vol.4
, pp. 3852
-
-
Song, C.E.1
Yang, J.W.2
Roh, Y.E.3
Lee, S.-G.4
Ahn, J.H.5
Han, H.6
-
52
-
-
0037121442
-
-
B.M. Trost, Z. Pan, J. Zambrano, and C. Kujat Angew. Chem., Int. Ed. Engl. 41 2002 4691
-
(2002)
Angew. Chem., Int. Ed. Engl.
, vol.41
, pp. 4691
-
-
Trost, B.M.1
Pan, Z.2
Zambrano, J.3
Kujat, C.4
-
55
-
-
0001712872
-
-
D.J. Bayston, J.L. Fraser, M.R. Ashton, A.D. Baxter, M.E. Polywka, and E. Moses J. Org. Chem. 63 1998 3137
-
(1998)
J. Org. Chem.
, vol.63
, pp. 3137
-
-
Bayston, D.J.1
Fraser, J.L.2
Ashton, M.R.3
Baxter, A.D.4
Polywka, M.E.5
Moses, E.6
-
57
-
-
4444307831
-
-
note
-
Key advantages of PS-PEG resin are as follows: (a) PS-PEG resin exhibits good swelling ability in a range of solvents (from water to toluene), which can be helpful in extraction of organic compounds and removal of reagent-derived ionic (or inorganic) co-products from the reaction beads. (b) It has been postulated that molecules (catalytic species) attached to the ends of long, flexible PEG chains are in a solution-like environment to show good activity in a given reaction.
-
-
-
-
58
-
-
4444357151
-
-
note
-
Key advantages of PS-PEG resin are as follows: (a) PS-PEG resin exhibits good swelling ability in a range of solvents (from water to toluene), which can be helpful in extraction of organic compounds and removal of reagent-derived ionic (or inorganic) co-products from the reaction beads. (b) It has been postulated that molecules (catalytic species) attached to the ends of long, flexible PEG chains are in a solution-like environment to show good activity in a given reaction.
-
-
-
-
59
-
-
0003164579
-
-
Voelter, W., Bayer, E., Ovchinikov, Y. A., Iwanov, V. T., Eds.; Walter de Gruter: Berlin
-
(a) Bayer, E.; Rapp, W. In Chemistry of Peptides and Proteins; Voelter, W., Bayer, E., Ovchinikov, Y. A., Iwanov, V. T., Eds.; Walter de Gruter: Berlin, 1986; Vol. 3, p 3.
-
(1986)
Chemistry of Peptides and Proteins
, vol.3
, pp. 3
-
-
Bayer, E.1
Rapp, W.2
-
62
-
-
0001102436
-
-
O.W. Gooding, S. Baudert, T.L. Deegan, K. Heisler, J.W. Labadie, W.S. Newcomb, J.A. Porco Jr., and P. Eikeren J. Comb. Chem. 1 1999 113
-
(1999)
J. Comb. Chem.
, vol.1
, pp. 113
-
-
Gooding, O.W.1
Baudert, S.2
Deegan, T.L.3
Heisler, K.4
Labadie, J.W.5
Newcomb, W.S.6
Porco Jr., J.A.7
Eikeren, P.8
-
68
-
-
33751157286
-
-
D. Cai, J.F. Payack, D.R. Bender, D.L. Hughes, T.R. Verhoeven, and P.J. Reider J. Org. Chem. 59 1994 7180
-
(1994)
J. Org. Chem.
, vol.59
, pp. 7180
-
-
Cai, D.1
Payack, J.F.2
Bender, D.R.3
Hughes, D.L.4
Verhoeven, T.R.5
Reider, P.J.6
-
69
-
-
0032586603
-
-
K. Nozaki, F. Shibahara, Y. Itoi, E. Shirakawa, T. Ohta, H. Takaya, and T. Hiyama Bull. Chem. Soc. Jpn 72 1999 1911
-
(1999)
Bull. Chem. Soc. Jpn
, vol.72
, pp. 1911
-
-
Nozaki, K.1
Shibahara, F.2
Itoi, Y.3
Shirakawa, E.4
Ohta, T.5
Takaya, H.6
Hiyama, T.7
-
70
-
-
0035936752
-
-
For typical examples, see: T. Hayashi, S. Hirate, K. Kitayama, H. Tsuji, A. Torii, and Y. Uozumi J. Org. Chem. 66 2001 1441
-
(2001)
J. Org. Chem.
, vol.66
, pp. 1441
-
-
Hayashi, T.1
Hirate, S.2
Kitayama, K.3
Tsuji, H.4
Torii, A.5
Uozumi, Y.6
-
71
-
-
4444235452
-
-
note
-
After the reaction, the catalyst beads were removed by filtration and the resulting filtrate did not catalyze the allylic reduction to demonstrate no leaching of palladium species from the beads during the catalytic reaction.
-
-
-
|