-
2
-
-
33846053281
-
-
P. A. Grieco Ed, Blackie Academic, London
-
(b) Organic Synthesis in Water, P. A. Grieco (Ed.), Blackie Academic, London (1998);
-
(1998)
Synthesis in Water
-
-
Organic1
-
5
-
-
24044470646
-
-
(e) C.-J. Li. Chem. Rev. 105, 3095 (2005).
-
(2005)
Chem. Rev
, vol.105
, pp. 3095
-
-
Li, C.-J.1
-
7
-
-
84955394357
-
-
H. Yamamoto Ed, Wiley-VCH, Weinheim
-
(b) H. Yamamoto (Ed.). Lewis Acids in Organic Synthesis, Wiley-VCH, Weinheim (2000);
-
(2000)
Lewis Acids in Organic Synthesis
-
-
-
8
-
-
0001000536
-
Lewis acid catalysis and the reactions of coordinated ligands
-
For an early review on reactions mediated by Lewis acidic metal cations in water, see (c, G. Wilkinson, R. D. Gillard, J. A. McCleverty Eds, p, Pergamon Press, Oxford
-
For an early review on reactions mediated by Lewis acidic metal cations in water, see (c) R. W. Hay. "Lewis acid catalysis and the reactions of coordinated ligands", in Comprehensive Coordination Chemistry, Vol. 6, G. Wilkinson, R. D. Gillard, J. A. McCleverty (Eds.), p. 411, Pergamon Press, Oxford (1987).
-
(1987)
Comprehensive Coordination Chemistry
, vol.6
, pp. 411
-
-
Hay, R.W.1
-
9
-
-
0001845652
-
Lanthanide triflate-catalyzed carbon-carbon bond-forming reactions in organic synthesis
-
S. Kobayashi Ed, p, Springer, Heidelberg
-
(a) S. Kobayashi. "Lanthanide triflate-catalyzed carbon-carbon bond-forming reactions in organic synthesis", in Lanthanides: Chemistry and Use in Organic Synthesis, S. Kobayashi (Ed.), p. 63, Springer, Heidelberg (1999);
-
(1999)
Lanthanides: Chemistry and Use in Organic Synthesis
, pp. 63
-
-
Kobayashi, S.1
-
12
-
-
0036625262
-
-
(d) S. Kobayashi, M. Sugiura, H. Kitagawa, W. W.-L. Lam. Chem. Rev. 102, 2227 (2002).
-
(2002)
Chem. Rev
, vol.102
, pp. 2227
-
-
Kobayashi, S.1
Sugiura, M.2
Kitagawa, H.3
Lam, W.W.-L.4
-
18
-
-
0002950518
-
Coordination Chemistry
-
2, A. E. Martell Ed, American Chemical Society, Washington, DC
-
(c) Coordination Chemistry, ACS Monograph 174, Vol. 2, A. E. Martell (Ed.), American Chemical Society, Washington, DC (1978).
-
(1978)
ACS Monograph
, vol.174
-
-
-
19
-
-
0035906461
-
-
4. F. Fringuelli, F. Pizzo, L. Vaccaro. J. Org. Chem. 66, 3554 (2001).
-
4. F. Fringuelli, F. Pizzo, L. Vaccaro. J. Org. Chem. 66, 3554 (2001).
-
-
-
-
25
-
-
0037433497
-
-
(d) T. Hamada, K. Manabe, S. Ishikawa, S. Nagayama, M. Shiro, S. Kobayashi. J. Am. Chem. Soc. 125, 2989 (2003);
-
(2003)
J. Am. Chem. Soc
, vol.125
, pp. 2989
-
-
Hamada, T.1
Manabe, K.2
Ishikawa, S.3
Nagayama, S.4
Shiro, M.5
Kobayashi, S.6
-
26
-
-
0042819676
-
-
(e) T. Hamada, K. Manabe, S. Kobayashi. Angew. Chem., Int. Ed. 42, 3927 (2003);
-
(2003)
Angew. Chem., Int. Ed
, vol.42
, pp. 3927
-
-
Hamada, T.1
Manabe, K.2
Kobayashi, S.3
-
30
-
-
33846914779
-
-
Catalytic asymmetric hydroxymethylation without using silicon enolates: (a) M. Fujii, Y. Sato, T. Aida, M. Yoshihara. Chem. Express 7, 309 (1992);
-
Catalytic asymmetric hydroxymethylation without using silicon enolates: (a) M. Fujii, Y. Sato, T. Aida, M. Yoshihara. Chem. Express 7, 309 (1992);
-
-
-
-
32
-
-
2942641357
-
-
(c) H. Torii, M. Nakadai, K. Ishihara, S. Saito, H. Yamamoto. Angew. Chem., Int. Ed. 43, 1983 (2004).
-
(2004)
Angew. Chem., Int. Ed
, vol.43
, pp. 1983
-
-
Torii, H.1
Nakadai, M.2
Ishihara, K.3
Saito, S.4
Yamamoto, H.5
-
33
-
-
0005696762
-
-
For a review on silicon enolates, see:, D. Bellus, S. V. Ley, R. Noyori, M. Regitz, E. Schaumann, I. Shinkai, E. J. Thomas, B. M. Trost Eds, p, Georg Thieme Verlag, Stuttgart
-
For a review on silicon enolates, see: S. Kobayashi, K. Manabe, H. Ishitani, J. Matsuo. In Science of Synthesis, Houben-Weyl Methods of Molecular Transformation, Vol. 4, D. Bellus, S. V. Ley, R. Noyori, M. Regitz, E. Schaumann, I. Shinkai, E. J. Thomas, B. M. Trost (Eds.), p. 317, Georg Thieme Verlag, Stuttgart (2002).
-
(2002)
Science of Synthesis, Houben-Weyl Methods of Molecular Transformation
, vol.4
, pp. 317
-
-
Kobayashi, S.1
Manabe, K.2
Ishitani, H.3
Matsuo, J.4
-
34
-
-
0034678591
-
-
For reviews on asymmetric aldol reactions, see: a
-
For reviews on asymmetric aldol reactions, see: (a) T. D. Machajewski, C.-H. Wong. Angew. Chem., Int. Ed. 39, 1352 (2000);
-
(2000)
Angew. Chem., Int. Ed
, vol.39
, pp. 1352
-
-
Machajewski, T.D.1
Wong, C.-H.2
-
35
-
-
0001702357
-
-
E. N. Jacobsen, A. Pflatz, H. Yamamoto Eds, p, Springer, Heidelberg
-
(b) E. M. Carreira. Comprehensive Asymmetric Catalysis, Vol. 3, E. N. Jacobsen, A. Pflatz, H. Yamamoto (Eds.), p. 998, Springer, Heidelberg (1999);
-
(1999)
Comprehensive Asymmetric Catalysis
, vol.3
, pp. 998
-
-
Carreira, E.M.1
-
37
-
-
33847804804
-
-
Trioxane was used as a formaldehyde surrogate: T. Mukaiyama, K. Banno, K. Narasaka. J. Am. Chem. Soc. 96, 7503 (1974).
-
Trioxane was used as a formaldehyde surrogate: T. Mukaiyama, K. Banno, K. Narasaka. J. Am. Chem. Soc. 96, 7503 (1974).
-
-
-
-
39
-
-
45549119177
-
-
For hydroxymethylation of a silicon enolate in aqueous media without any catalysts, see
-
(b) For hydroxymethylation of a silicon enolate in aqueous media without any catalysts, see: A. Lubineau, E. Meyer. Tetrahedron 44, 6065 (1988).
-
(1988)
Tetrahedron
, vol.44
, pp. 6065
-
-
Lubineau, A.1
Meyer, E.2
-
40
-
-
0346789075
-
-
K. Manabe, S. Ishikawa, T. Hamada, S. Kobayashi. Tetrahedron 59, 10439 (2003).
-
(2003)
Tetrahedron
, vol.59
, pp. 10439
-
-
Manabe, K.1
Ishikawa, S.2
Hamada, T.3
Kobayashi, S.4
-
42
-
-
33846917599
-
-
3: 22 h, 75 % yield, 83 % ee].
-
3: 22 h, 75 % yield, 83 % ee].
-
-
-
-
43
-
-
0035814327
-
-
3-complexes with chiral ligands: (a) D. A. Evans, Z. K. Sweeney, T. Rovis, J. S. Tedrow. J. Am. Chem. Soc. 123, 12095 (2001);
-
3-complexes with chiral ligands: (a) D. A. Evans, Z. K. Sweeney, T. Rovis, J. S. Tedrow. J. Am. Chem. Soc. 123, 12095 (2001);
-
-
-
-
44
-
-
0042233997
-
-
(b) D. A. Evans, K. A. Scheidt, K. R. Fandrick, H. W. Lam, J. Wu. J. Am. Chem. Soc. 125, 10780 (2003).
-
(2003)
J. Am. Chem. Soc
, vol.125
, pp. 10780
-
-
Evans, D.A.1
Scheidt, K.A.2
Fandrick, K.R.3
Lam, H.W.4
Wu, J.5
-
45
-
-
0032437210
-
-
(a) P. L. Baliri, G. Catelani, R. Giori, E. Mastrorilli. Enantiomer 3, 357 (1998);
-
(1998)
Enantiomer
, vol.3
, pp. 357
-
-
Baliri, P.L.1
Catelani, G.2
Giori, R.3
Mastrorilli, E.4
-
46
-
-
0033551905
-
-
(b) H. Miyaoka, Y. Kajiwara, M. Hara, A. Suma, Y. Yamada. Tetrahedron: Asymmetry 10, 3189 (1999).
-
(1999)
Tetrahedron: Asymmetry
, vol.10
, pp. 3189
-
-
Miyaoka, H.1
Kajiwara, Y.2
Hara, M.3
Suma, A.4
Yamada, Y.5
-
48
-
-
0037016958
-
-
(b) S. Répichet, A. Zwick, L. Vendier, C. Le Roux, J. Dubac. Tetrahedron Lett. 43, 993 (2002).
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 993
-
-
Répichet, S.1
Zwick, A.2
Vendier, L.3
Le Roux, C.4
Dubac, J.5
-
49
-
-
0037016958
-
-
S. Répichet, A. Zwick, L. Vendier, C. Le Roux, J. Dubac. Tetrahedron Lett. 43, 993 (2002).
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 993
-
-
Répichet, S.1
Zwick, A.2
Vendier, L.3
Le Roux, C.4
Dubac, J.5
-
50
-
-
33846934869
-
-
3 is a water-compatible Lewis acid, and it works well for hydroxymethylation even in the absence of a basic ligand. S. Kobayashi, I. Hachiya, H. Ishitani, M. Araki. Synlett 472 (1993).
-
3 is a water-compatible Lewis acid, and it works well for hydroxymethylation even in the absence of a basic ligand. S. Kobayashi, I. Hachiya, H. Ishitani, M. Araki. Synlett 472 (1993).
-
-
-
-
51
-
-
27144472960
-
-
S. Kobayashi, T. Ogino, H. Shimizu, S. Ishikawa, T. Hamada, K. Manabe. Org. Lett. 7, 4729 (2005).
-
(2005)
Org. Lett
, vol.7
, pp. 4729
-
-
Kobayashi, S.1
Ogino, T.2
Shimizu, H.3
Ishikawa, S.4
Hamada, T.5
Manabe, K.6
-
52
-
-
33846928366
-
-
The angle of O-Bi-O is 165°, while that of O-Sc-O is 151°. The torsional angle of two pyridines in the Bi complex is 27.0°, and that in the Sc complex is 19.4°. For the Sc complex, see ref. [13].
-
The angle of O-Bi-O is 165°, while that of O-Sc-O is 151°. The torsional angle of two pyridines in the Bi complex is 27.0°, and that in the Sc complex is 19.4°. For the Sc complex, see ref. [13].
-
-
-
-
53
-
-
0038468227
-
-
For reviews on the asymmetric synthesis and use of vicinal amino alcohols, see: a
-
For reviews on the asymmetric synthesis and use of vicinal amino alcohols, see: (a) D. J. Ager, I. Prakash, D. R. Schaad. Chem. Rev. 96, 835 (1996);
-
(1996)
Chem. Rev
, vol.96
, pp. 835
-
-
Ager, D.J.1
Prakash, I.2
Schaad, D.R.3
-
56
-
-
0001030240
-
-
M. Beller, C. Bolm, Eds, p, Wiley-VCH, Weinheim
-
(d) H. C. Kolb, K. B. Sharpless. In Transition Metals for Organic Synthesis, M. Beller, C. Bolm, (Eds.), p. 243, Wiley-VCH, Weinheim (1998).
-
(1998)
Transition Metals for Organic Synthesis
, pp. 243
-
-
Kolb, H.C.1
Sharpless, K.B.2
-
57
-
-
0032557714
-
-
(a) X. L. Hou, J. Wu, L. X. Dai, L. J. Xia, M. H. Tang. Tetrahedron: Asymmetry 9, 1747 (1998);
-
(1998)
Tetrahedron: Asymmetry
, vol.9
, pp. 1747
-
-
Hou, X.L.1
Wu, J.2
Dai, L.X.3
Xia, L.J.4
Tang, M.H.5
-
58
-
-
0033603374
-
-
(b) S. Sagawa, H. Abe, Y. Hase, T. Inaba. J. Org. Chem. 64, 4962 (1999);
-
(1999)
J. Org. Chem
, vol.64
, pp. 4962
-
-
Sagawa, S.1
Abe, H.2
Hase, Y.3
Inaba, T.4
-
60
-
-
8444233967
-
-
(d) C. Schneider, A. R. Sreekanth, E. Mai. Angew. Chem., Int. Ed. 43, 5691 (2004);
-
(2004)
Angew. Chem., Int. Ed
, vol.43
, pp. 5691
-
-
Schneider, C.1
Sreekanth, A.R.2
Mai, E.3
-
62
-
-
0034596298
-
-
K. Manabe, Y. Mori, T. Wakabayashi, W. Nagayama, S. Kobayashi. J. Am. Chem. Soc. 122, 7202 (2000).
-
(2000)
J. Am. Chem. Soc
, vol.122
, pp. 7202
-
-
Manabe, K.1
Mori, Y.2
Wakabayashi, T.3
Nagayama, W.4
Kobayashi, S.5
-
67
-
-
0041818324
-
-
For examples of racemic epoxide ring-opening in water, see, a N. Iranpoor, H. Firouzabadi, M. Shekarize. Org. Biomol. Chem. 1, 724 (2003);
-
For examples of racemic epoxide ring-opening in water, see : (a) N. Iranpoor, H. Firouzabadi, M. Shekarize. Org. Biomol. Chem. 1, 724 (2003);
-
-
-
-
73
-
-
0000862669
-
-
For reviews on asymmetric Mannich reactions, see: a
-
For reviews on asymmetric Mannich reactions, see: (a) S. Kobayashi, H. Ishitani. Chem. Rev. 99, 1069 (1999);
-
(1999)
Chem. Rev
, vol.99
, pp. 1069
-
-
Kobayashi, S.1
Ishitani, H.2
-
75
-
-
10844266525
-
-
E. N. Jacobsen, A. Pfaltz, H. Yamamoto Eds, Chap. 29.5, pp, Springer, Berlin
-
(c) S. Kobayashi, M. Ueno. In Comprehensive Asymmetric Catalysis, E. N. Jacobsen, A. Pfaltz, H. Yamamoto (Eds.), Supplement 1, Chap. 29.5, pp. 143-159, Springer, Berlin (2004).
-
(2004)
Comprehensive Asymmetric Catalysis
, Issue.SUPPL.EMENT 1
, pp. 143-159
-
-
Kobayashi, S.1
Ueno, M.2
-
76
-
-
0005696762
-
-
D. Bellus, S. V. Ley, R. Noyori, M. Regitz, E. Schauman, I. Shinkai, E. J. Thomas, B. M. Trost, Eds, pp, Georg Thieme Verlag, Stuttgart
-
S. Kobayashi, K. Manabe, H. Ishitani, J. Matsuo. In Science of Synthesis, Houben-Weyl Methods of Molecular Transformations, Vol. 4, D. Bellus, S. V. Ley, R. Noyori, M. Regitz, E. Schauman, I. Shinkai, E. J. Thomas, B. M. Trost. (Eds.), pp. 317-369, Georg Thieme Verlag, Stuttgart (2002).
-
(2002)
Science of Synthesis, Houben-Weyl Methods of Molecular Transformations
, vol.4
, pp. 317-369
-
-
Kobayashi, S.1
Manabe, K.2
Ishitani, H.3
Matsuo, J.4
-
77
-
-
0345529038
-
-
After our first report [35], some reports on catalytic asymmetric Mannich reactions in aqueous media appeared: (a) N. Wolfgang, F. Tanaka, S.-i. Watanabe, N. S. Chowdari, J. M. Turner, R. Thayumanavan, C. F. Barbas III. J. Org. Chem. 68, 9624 (2003);
-
After our first report [35], some reports on catalytic asymmetric Mannich reactions in aqueous media appeared: (a) N. Wolfgang, F. Tanaka, S.-i. Watanabe, N. S. Chowdari, J. M. Turner, R. Thayumanavan, C. F. Barbas III. J. Org. Chem. 68, 9624 (2003);
-
-
-
-
79
-
-
11144333506
-
-
(c) I. Ibrahem, J. Casas, A. Córdova. Angew. Chem., Int. Ed. 43, 6528 (2004).
-
(2004)
Angew. Chem., Int. Ed
, vol.43
, pp. 6528
-
-
Ibrahem, I.1
Casas, J.2
Córdova, A.3
-
82
-
-
0001141046
-
-
For review on Mannich reactions, see: a
-
For review on Mannich reactions, see: (a) M. Arend, B. Westermann, N. Risch. Angew. Chem. 110, 1096 (1998);
-
(1998)
Angew. Chem
, vol.110
, pp. 1096
-
-
Arend, M.1
Westermann, B.2
Risch, N.3
-
83
-
-
0032482080
-
-
(b) M. Arend, B. Westermann, N. Risch. Angew. Chem., Int. Ed. 37, 1044 (1998).
-
(1998)
Angew. Chem., Int. Ed
, vol.37
, pp. 1044
-
-
Arend, M.1
Westermann, B.2
Risch, N.3
-
84
-
-
84944149422
-
-
Burk reported catalytic asymmetric hydrogenations of N- acylhydrazones: M. J. Burk, J. E. Feaster. J. Am. Chem. Soc. 114, 6266 (1992).
-
Burk reported catalytic asymmetric hydrogenations of N- acylhydrazones: M. J. Burk, J. E. Feaster. J. Am. Chem. Soc. 114, 6266 (1992).
-
-
-
-
87
-
-
0032694974
-
-
(c) K. Manabe, H. Oyamada, K. Sugita, S. Kobayashi. J. Org. Chem. 64, 8054 (1999).
-
(1999)
J. Org. Chem
, vol.64
, pp. 8054
-
-
Manabe, K.1
Oyamada, H.2
Sugita, K.3
Kobayashi, S.4
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