-
1
-
-
72149083418
-
-
For selected reviews, see
-
For selected reviews, see:
-
-
-
-
8
-
-
47749122232
-
-
Berkessel A., and Gröger H. (Eds), Wiley-VCH, Weinheim
-
In: Berkessel A., and Gröger H. (Eds). Asymmetric Organocatalysis (2005), Wiley-VCH, Weinheim
-
(2005)
Asymmetric Organocatalysis
-
-
-
9
-
-
55049138759
-
-
Dalko P.I. (Ed), Wiley-VCH, Weinheim
-
In: Dalko P.I. (Ed). Enantioselective Organocatalysis (2007), Wiley-VCH, Weinheim
-
(2007)
Enantioselective Organocatalysis
-
-
-
10
-
-
72149120972
-
-
For selected reviews, see
-
For selected reviews, see:
-
-
-
-
15
-
-
72149124635
-
-
For recent literature using primary amine catalysts, see
-
For recent literature using primary amine catalysts, see:
-
-
-
-
21
-
-
72149093365
-
-
For selected recent literature, see
-
For selected recent literature, see:
-
-
-
-
25
-
-
21244479264
-
-
Tang Z., Yang Z.-H., Chen X.-H., Cun L.-F., Mi A.-Q., Jiang Y.-Z., and Gong L.-Z. J. Am. Chem. Soc. 127 (2005) 9285
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 9285
-
-
Tang, Z.1
Yang, Z.-H.2
Chen, X.-H.3
Cun, L.-F.4
Mi, A.-Q.5
Jiang, Y.-Z.6
Gong, L.-Z.7
-
27
-
-
43049123662
-
-
Xu D.-Q., Wang L.-P., Luo S.-P., Wang Y.-F., Zhang S., and Xu Z.-Y. Eur. J. Org. Chem. (2008) 1049
-
(2008)
Eur. J. Org. Chem.
, pp. 1049
-
-
Xu, D.-Q.1
Wang, L.-P.2
Luo, S.-P.3
Wang, Y.-F.4
Zhang, S.5
Xu, Z.-Y.6
-
31
-
-
68949152712
-
-
Lu A., Gao P., Wu Y., Wang Y., Zhou Z., and Tang C. Org. Biomol. Chem. 7 (2009) 3141
-
(2009)
Org. Biomol. Chem.
, vol.7
, pp. 3141
-
-
Lu, A.1
Gao, P.2
Wu, Y.3
Wang, Y.4
Zhou, Z.5
Tang, C.6
-
32
-
-
70349761379
-
-
Chen J.-R., Lai Y.-Y., Lu H.-H., Wang X.-F., and Xiao W.-J. Tetrahedron 65 (2009) 9238
-
(2009)
Tetrahedron
, vol.65
, pp. 9238
-
-
Chen, J.-R.1
Lai, Y.-Y.2
Lu, H.-H.3
Wang, X.-F.4
Xiao, W.-J.5
-
33
-
-
72149111527
-
-
For selected recent literature, see
-
For selected recent literature, see:
-
-
-
-
34
-
-
22144459070
-
-
Hayashi Y., Gotoh H., Hayashi T., and Shoji M. Angew. Chem., Int. Ed. 44 (2005) 4212
-
(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 4212
-
-
Hayashi, Y.1
Gotoh, H.2
Hayashi, T.3
Shoji, M.4
-
37
-
-
33745542958
-
-
Mossé S., Laars M., Kriis K., Kanger T., and Alexakis A. Org. Lett. 8 (2006) 2559
-
(2006)
Org. Lett.
, vol.8
, pp. 2559
-
-
Mossé, S.1
Laars, M.2
Kriis, K.3
Kanger, T.4
Alexakis, A.5
-
40
-
-
72149112068
-
-
For selected recent literature, see
-
For selected recent literature, see:
-
-
-
-
41
-
-
33646142092
-
-
Mase N., Watanabe K., Yoda H., Takabe K., Tanaka F., and Barbas III C.F. J. Am. Chem. Soc. 128 (2006) 4966
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 4966
-
-
Mase, N.1
Watanabe, K.2
Yoda, H.3
Takabe, K.4
Tanaka, F.5
Barbas III, C.F.6
-
43
-
-
33746216402
-
-
Luo S., Mi X., Zhang L., Liu S., Xu H., and Cheng J. Angew. Chem., Int. Ed. 45 (2006) 3093
-
(2006)
Angew. Chem., Int. Ed.
, vol.45
, pp. 3093
-
-
Luo, S.1
Mi, X.2
Zhang, L.3
Liu, S.4
Xu, H.5
Cheng, J.6
-
44
-
-
66149154333
-
-
Tan B., Zeng X., Lu Y., Chua P.J., and Zhong G. Org. Lett. 11 (2009) 1927
-
(2009)
Org. Lett.
, vol.11
, pp. 1927
-
-
Tan, B.1
Zeng, X.2
Lu, Y.3
Chua, P.J.4
Zhong, G.5
-
45
-
-
58549093369
-
-
An excellent review for stereoselective organocatalytic reactions using water including asymmetric Michael addition, see and references therein
-
An excellent review for stereoselective organocatalytic reactions using water including asymmetric Michael addition, see. Gruttadauria M., Giacalone F., and Noto R. Adv. Synth. Catal. 351 (2009) 33 and references therein
-
(2009)
Adv. Synth. Catal.
, vol.351
, pp. 33
-
-
Gruttadauria, M.1
Giacalone, F.2
Noto, R.3
-
46
-
-
72149103107
-
-
For recent application of these reactions on water, see
-
For recent application of these reactions on water, see:
-
-
-
-
47
-
-
20344388819
-
-
Narayan S., Muldoon J., Finn M.G., Fokin V.V., Kolb H.C., and Sharpless K.B. Angew. Chem., Int. Ed. 44 (2005) 3275
-
(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 3275
-
-
Narayan, S.1
Muldoon, J.2
Finn, M.G.3
Fokin, V.V.4
Kolb, H.C.5
Sharpless, K.B.6
-
49
-
-
34250726521
-
-
Blackmond D.G., Armstrong A., Coombe V., and Wells A. Angew. Chem., Int. Ed. 46 (2007) 3798
-
(2007)
Angew. Chem., Int. Ed.
, vol.46
, pp. 3798
-
-
Blackmond, D.G.1
Armstrong, A.2
Coombe, V.3
Wells, A.4
-
52
-
-
0038023865
-
-
The selected literature for its preparation
-
The selected literature for its preparation. Bartoli G., Bosco M., Dalpozzo R., Giuliani A., Marcantoni E., Mecozzi T., Sambri L., and Torregiani E. J. Org. Chem. 67 (2002) 9111
-
(2002)
J. Org. Chem.
, vol.67
, pp. 9111
-
-
Bartoli, G.1
Bosco, M.2
Dalpozzo, R.3
Giuliani, A.4
Marcantoni, E.5
Mecozzi, T.6
Sambri, L.7
Torregiani, E.8
-
54
-
-
0030757959
-
-
For the preparation of compound 2a, see:
-
For the preparation of compound 2a, see:. Hart D.J., Li J., and Wu W.-L.J. Org. Chem. 62 (1997) 5023
-
(1997)
Org. Chem.
, vol.62
, pp. 5023
-
-
Hart, D.J.1
Li, J.2
Wu, W.-L.J.3
-
55
-
-
0035263817
-
-
For the application of pyrrolidine-derived sulfide in asymmetric addition of dialkyzinc toward aldehyde, see:
-
For the application of pyrrolidine-derived sulfide in asymmetric addition of dialkyzinc toward aldehyde, see:. Pu L., and Yu H.-B. Chem. Rev. 101 (2001) 757
-
(2001)
Chem. Rev.
, vol.101
, pp. 757
-
-
Pu, L.1
Yu, H.-B.2
-
56
-
-
72149093074
-
-
For the application of Michael addition adducts, see
-
For the application of Michael addition adducts, see:
-
-
-
-
59
-
-
0037028924
-
-
Córdova A., Notz W., Zhong G., Betancort J.M., and Barbas III C.F. J. Am. Chem. Soc. 124 (2002) 1842
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 1842
-
-
Córdova, A.1
Notz, W.2
Zhong, G.3
Betancort, J.M.4
Barbas III, C.F.5
-
60
-
-
0037028990
-
-
Córdova A., Watanabe S., Tanaka F., Notz W., and Barbas III C.F. J. Am. Chem. Soc. 124 (2002) 1866
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 1866
-
-
Córdova, A.1
Watanabe, S.2
Tanaka, F.3
Notz, W.4
Barbas III, C.F.5
-
61
-
-
0037799595
-
-
For the preparation of aryl nitroolefins
-
For the preparation of aryl nitroolefins. Jang Y.-J., Shih Y.-K., Liu J.-Y., Kuo W.-Y., and Yao C.-F. Chem.- Eur. J. 9 (2003) 2123
-
(2003)
Chem.- Eur. J.
, vol.9
, pp. 2123
-
-
Jang, Y.-J.1
Shih, Y.-K.2
Liu, J.-Y.3
Kuo, W.-Y.4
Yao, C.-F.5
-
62
-
-
72149118310
-
-
For the product 5a, 5l, and 6, see: . ;
-
For the product 5a, 5l, and 6, see: Ref. 4b;
-
, vol.4 b
-
-
Ref1
-
63
-
-
72149117230
-
-
For 5b, and 5k, see: . ;
-
For 5b, and 5k, see: Ref. 4i;
-
, vol.4 i
-
-
Ref1
-
64
-
-
11844253794
-
-
For 5m, see: Ref. 4h;
-
For 5m, see:. Cobb A.J.A., Shaw D.M., Longbottom D.A., Gold J.B., and Ley S.V. Org. Biomol. Chem. 3 (2005) 84 Ref. 4h;
-
(2005)
Org. Biomol. Chem.
, vol.3
, pp. 84
-
-
Cobb, A.J.A.1
Shaw, D.M.2
Longbottom, D.A.3
Gold, J.B.4
Ley, S.V.5
-
65
-
-
72149089433
-
-
For 5d, and 5f, see
-
For 5d, and 5f, see: Refs. 6b and 9d;
-
6b and 9d
-
-
Refs1
-
66
-
-
72149108840
-
-
For 5i, see: Ref. 6c;
-
For 5i, see: Ref. 6c;
-
-
-
-
67
-
-
72149118568
-
-
For 5e and 5j, see: . ;
-
For 5e and 5j, see: Ref. 7;
-
, vol.7
-
-
Ref1
-
68
-
-
38849124986
-
-
For 5c, see:
-
For 5c, see:. Luo S., Li J., Zhang L., Xu H., and Cheng J.-P. Chem.- Eur. J. 14 (2008) 1273
-
(2008)
Chem.- Eur. J.
, vol.14
, pp. 1273
-
-
Luo, S.1
Li, J.2
Zhang, L.3
Xu, H.4
Cheng, J.-P.5
-
69
-
-
33751581895
-
-
For 5g, see:
-
For 5g, see:. Luo S., Xu H., Mi X., Li J., Zheng X., and Cheng J.-P. J. Org. Chem. 71 (2006) 9244
-
(2006)
J. Org. Chem.
, vol.71
, pp. 9244
-
-
Luo, S.1
Xu, H.2
Mi, X.3
Li, J.4
Zheng, X.5
Cheng, J.-P.6
-
71
-
-
34250618376
-
-
For 7, see:
-
For 7, see:. Almasi D., Alonso D.A., Gómez-Bengoa E., Nagel Y., and Nájera C. Eur. J. Org. Chem. (2007) 2328
-
(2007)
Eur. J. Org. Chem.
, pp. 2328
-
-
Almasi, D.1
Alonso, D.A.2
Gómez-Bengoa, E.3
Nagel, Y.4
Nájera, C.5
-
72
-
-
67549084539
-
-
For 9, see:
-
For 9, see:. Chang C., Li S.-H., Reddy R.J., and Chen K. Adv. Synth. Catal. 351 (2009) 1273
-
(2009)
Adv. Synth. Catal.
, vol.351
, pp. 1273
-
-
Chang, C.1
Li, S.-H.2
Reddy, R.J.3
Chen, K.4
|