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-
-
Fujioka, H.1
Murai, K.2
Ohba, Y.3
Hiramatsu, A.4
Kita, Y.5
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64
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33745003466
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-
Recently, preparations of similar m-phebims from chiral amino alcohols have been reported, see: a X. Hao, J. Gong, C. Du, L. Wu, Y. Wu, M. Song, Tetrahedron Lett. 2006, 47, 5033-5036;
-
Recently, preparations of similar m-phebims from chiral amino alcohols have been reported, see: a) X. Hao, J. Gong, C. Du, L. Wu, Y. Wu, M. Song, Tetrahedron Lett. 2006, 47, 5033-5036;
-
-
-
-
65
-
-
34447515577
-
-
[2b,h]
-
[2b,h]
-
-
-
-
66
-
-
34250630793
-
-
For recent reviews of bis(oxazolyl)phenyl ligand (Phebox), see: a) H. Nishiyama, Chem. Soc. Rev. 2007, 36, 1133-1141;
-
For recent reviews of bis(oxazolyl)phenyl ligand (Phebox), see: a) H. Nishiyama, Chem. Soc. Rev. 2007, 36, 1133-1141;
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-
-
-
68
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53849123022
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-
With various other Lewis acids such as CuOTf, Mg(OTf)2, Zn(OTf)2, and Sc(OTf)3, the enantioselectivity was lowered
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3, the enantioselectivity was lowered.
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-
-
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69
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17844379719
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For the reversal of the stereochemistry using the same chiral ligands or similar ones, see review: a
-
For the reversal of the stereochemistry using the same chiral ligands or similar ones, see review: a) M. P. Sibi, M. Liu, Curr. Org. Chem. 2001, 5, 719-755;
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(2001)
Curr. Org. Chem
, vol.5
, pp. 719-755
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Sibi, M.P.1
Liu, M.2
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70
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0033605831
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-
see also: b
-
see also: b) M. Kanai, Y. Nakagawa, K. Tomioka, Tetrahedron 1999, 55, 3831-3842;
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(1999)
Tetrahedron
, vol.55
, pp. 3831-3842
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-
Kanai, M.1
Nakagawa, Y.2
Tomioka, K.3
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72
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4143150689
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-
d) N. Shibata, T. Ishimaru, T. Nagai, J. Kohno, T. Toru, Synlett 2004, 1703-1706;
-
(2004)
Synlett
, pp. 1703-1706
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-
Shibata, N.1
Ishimaru, T.2
Nagai, T.3
Kohno, J.4
Toru, T.5
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73
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2142704287
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-
e) S. Nakamura, N. Sato, M. Sugimoto, T. Toru, Tetrahedron: Asymmetry 2004, 15, 1513-1516;
-
(2004)
Tetrahedron: Asymmetry
, vol.15
, pp. 1513-1516
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Nakamura, S.1
Sato, N.2
Sugimoto, M.3
Toru, T.4
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74
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2342472565
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f) C. P. Casey, S. C. Martins, M. A. Fagan, J. Am. Chem. Soc. 2004, 126, 5585-5592;
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(2004)
J. Am. Chem. Soc
, vol.126
, pp. 5585-5592
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Casey, C.P.1
Martins, S.C.2
Fagan, M.A.3
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75
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17744381382
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g) D. Du, S. Lu, T. Fang, J. Xu, J. Org. Chem. 2005, 70, 3712-3715;
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(2005)
J. Org. Chem
, vol.70
, pp. 3712-3715
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Du, D.1
Lu, S.2
Fang, T.3
Xu, J.4
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76
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33744830047
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-
h) N. Kato, T. Mita, M. Kanai, B. Therrien, M. Kawano, K. Yamaguchi, H. Danjo, Y. Sei, A. Sato, S. Furusho, M. Shibasaki, J. Am. Chem. Soc. 2006, 128, 6768-6769;
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 6768-6769
-
-
Kato, N.1
Mita, T.2
Kanai, M.3
Therrien, B.4
Kawano, M.5
Yamaguchi, K.6
Danjo, H.7
Sei, Y.8
Sato, A.9
Furusho, S.10
Shibasaki, M.11
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78
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53849124742
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2 afforded (S)-3a in 53% yield with 3% ee.
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2 afforded (S)-3a in 53% yield with 3% ee.
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-
-
-
79
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53849141545
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-
Molecular sieves 4 Å improved reproducibility of the reaction.
-
Molecular sieves 4 Å improved reproducibility of the reaction.
-
-
-
-
80
-
-
53849140494
-
-
2 afforded the products with low enantioselectivity.
-
2 afforded the products with low enantioselectivity.
-
-
-
-
81
-
-
53849098435
-
-
2+.
-
2+.
-
-
-
-
82
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-
37849002571
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-
A similar dual activation mechanism in the oxidation of tryptophan by human tryptophan dioxygenase has been reported, in which the activations by hydrogen bonding of indole to the imidazole nitrogen in histidine and by coordination of oxygen to Fe2+ are involved, see: D. Batabyal, S.-R. Yeh, J. Am. Chem. Soc. 2007, 129, 15690-15701
-
2+ are involved, see: D. Batabyal, S.-R. Yeh, J. Am. Chem. Soc. 2007, 129, 15690-15701.
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