-
10
-
-
62349088498
-
-
N. Steffan, A. Grundmann, W.-B. Yin, A. Kremer, and S.-M. Li Curr. Med. Chem. 16 2009 218 231
-
(2009)
Curr. Med. Chem.
, vol.16
, pp. 218-231
-
-
Steffan, N.1
Grundmann, A.2
Yin, W.-B.3
Kremer, A.4
Li, S.-M.5
-
12
-
-
78549240174
-
-
B.V.S. Reddy, M.R. Reddy, C. Madan, K.P. Kumar, and M.S. Rao Bioorg. Med. Chem. Lett. 20 2010 7507 7511
-
(2010)
Bioorg. Med. Chem. Lett.
, vol.20
, pp. 7507-7511
-
-
Reddy, B.V.S.1
Reddy, M.R.2
Madan, C.3
Kumar, K.P.4
Rao, M.S.5
-
13
-
-
72049126378
-
-
A. Rives, B. Le Calvé, T. Delaine, L. Legentil, R. Kiss, and E. Delfourne Eur. J. Med. Chem. 45 2010 343 351
-
(2010)
Eur. J. Med. Chem.
, vol.45
, pp. 343-351
-
-
Rives, A.1
Le Calvé, B.2
Delaine, T.3
Legentil, L.4
Kiss, R.5
Delfourne, E.6
-
14
-
-
79958851497
-
-
Y. Takahashi, T. Kubota, A. Shibazaki, T. Gonoi, J. Fromont, and J. Kobayashi Org. Lett. 13 2011 3016 3019
-
(2011)
Org. Lett.
, vol.13
, pp. 3016-3019
-
-
Takahashi, Y.1
Kubota, T.2
Shibazaki, A.3
Gonoi, T.4
Fromont, J.5
Kobayashi, J.6
-
19
-
-
33847630406
-
-
For non-asymmetric examples, see
-
For non-asymmetric examples, see: A. Palmieri, and M. Petrini J. Org. Chem. 72 2007 1863 1866
-
(2007)
J. Org. Chem.
, vol.72
, pp. 1863-1866
-
-
Palmieri, A.1
Petrini, M.2
-
30
-
-
60149089206
-
-
For asymmetric examples, see:, Angew. Chem., Int. Ed. 2008, 47, 8707-8710
-
For asymmetric examples, see: R.R. Shaikh, A. Mazzanti, M. Petrini, G. Bartoli, and P. Melchiorre Angew. Chem. 120 2008 8835 8838 Angew. Chem., Int. Ed. 2008, 47, 8707-8710
-
(2008)
Angew. Chem.
, vol.120
, pp. 8835-8838
-
-
Shaikh, R.R.1
Mazzanti, A.2
Petrini, M.3
Bartoli, G.4
Melchiorre, P.5
-
33
-
-
77956953064
-
-
L. Jing, J. Wei, L. Zhou, Z. Huang, Z. Li, D. Wu, H. Xiang, and X. Zhou Chem. Eur. J. 16 2010 10955 10958
-
(2010)
Chem. Eur. J.
, vol.16
, pp. 10955-10958
-
-
Jing, L.1
Wei, J.2
Zhou, L.3
Huang, Z.4
Li, Z.5
Wu, D.6
Xiang, H.7
Zhou, X.8
-
36
-
-
79960433687
-
-
J. Wang, S. Zhou, D. Lin, X. Ding, H. Jiang, and H. Liu Chem. Commun. 2011 8355 8357
-
(2011)
Chem. Commun.
, pp. 8355-8357
-
-
Wang, J.1
Zhou, S.2
Lin, D.3
Ding, X.4
Jiang, H.5
Liu, H.6
-
37
-
-
84860711465
-
-
M. Fochi, L. Gramigna, A. Mazzanti, S. Duce, S. Fantini, A. Palmieri, M. Petrini, and L. Bernardi Adv. Synth. Catal. 354 2012 1373 1380
-
(2012)
Adv. Synth. Catal.
, vol.354
, pp. 1373-1380
-
-
Fochi, M.1
Gramigna, L.2
Mazzanti, A.3
Duce, S.4
Fantini, S.5
Palmieri, A.6
Petrini, M.7
Bernardi, L.8
-
38
-
-
84869028817
-
-
X.-L. Zhu, W.-J. He, L.-L. Yu, C.-W. Cai, Z.-L. Zuo, D.-B. Qin, Q.-Z. Liu, and L.-H. Jing Adv. Synth. Catal. 354 2012 2965 2970
-
(2012)
Adv. Synth. Catal.
, vol.354
, pp. 2965-2970
-
-
Zhu, X.-L.1
He, W.-J.2
Yu, L.-L.3
Cai, C.-W.4
Zuo, Z.-L.5
Qin, D.-B.6
Liu, Q.-Z.7
Jing, L.-H.8
-
39
-
-
11144263200
-
-
For selected reviews and special issues, see: Angew. Chem., Int. Ed. 2004, 43, 5138-5175
-
For selected reviews and special issues, see: P.I. Dalko, and L. Moisan Angew. Chem. 116 2004 5248 5286 Angew. Chem., Int. Ed. 2004, 43, 5138-5175
-
(2004)
Angew. Chem.
, vol.116
, pp. 5248-5286
-
-
Dalko, P.I.1
Moisan, L.2
-
49
-
-
54749090942
-
-
Angew. Chem., Int. Ed. 2008, 47, 4638-4660
-
A. Dondoni, and A. Massi Angew. Chem. 120 2008 4716 4739 Angew. Chem., Int. Ed. 2008, 47, 4638-4660
-
(2008)
Angew. Chem.
, vol.120
, pp. 4716-4739
-
-
Dondoni, A.1
Massi, A.2
-
51
-
-
55249111616
-
-
Angew. Chem., Int. Ed. 2008, 47, 6138-6171
-
P. Melchiorre, M. Marigo, A. Carlone, and G. Bartoli Angew. Chem. 120 2008 6232 6265 Angew. Chem., Int. Ed. 2008, 47, 6138-6171
-
(2008)
Angew. Chem.
, vol.120
, pp. 6232-6265
-
-
Melchiorre, P.1
Marigo, M.2
Carlone, A.3
Bartoli, G.4
-
52
-
-
53349170687
-
-
Angew. Chem., Int. Ed. 2008, 47, 42-47
-
C.F. Barbas III Angew. Chem. 2008 120 2008 44 50 Angew. Chem., Int. Ed. 2008, 47, 42-47
-
(2008)
Angew. Chem.
, vol.2008
, Issue.120
, pp. 44-50
-
-
Barbas Iii, C.F.1
-
56
-
-
84878753079
-
-
Acc. Chem. Res. 2004, 37, 487-631; Tetrahedron 2006, 62, 243-502; Chem. Rev. 2007, 107, 5413-5883.
-
Special issues: Adv. Synth. Catal. 2004, 346, 1007-1249; Acc. Chem. Res. 2004, 37, 487-631; Tetrahedron 2006, 62, 243-502; Chem. Rev. 2007, 107, 5413-5883.
-
(2004)
Special Issues: Adv. Synth. Catal.
, vol.346
, pp. 1007-1249
-
-
-
57
-
-
0346865819
-
-
For selected recent reviews of (thio)urea-based organocatalysis, see
-
For selected recent reviews of (thio)urea-based organocatalysis, see: P.R. Schreiner Chem. Soc. Rev. 32 2003 289 296
-
(2003)
Chem. Soc. Rev.
, vol.32
, pp. 289-296
-
-
Schreiner, P.R.1
-
58
-
-
9244238796
-
-
Angew. Chem., Int. Ed. 2004, 43, 2062-2064
-
P.M. Pihko Angew. Chem. 116 2004 2110 2113 Angew. Chem., Int. Ed. 2004, 43, 2062-2064
-
(2004)
Angew. Chem.
, vol.116
, pp. 2110-2113
-
-
Pihko, P.M.1
-
63
-
-
33746322013
-
-
Angew. Chem., Int. Ed. 2006, 45, 1520-1543
-
M.S. Taylor, and E.N. Jacobsen Angew. Chem. 118 2006 1550 1573 Angew. Chem., Int. Ed. 2006, 45, 1520-1543
-
(2006)
Angew. Chem.
, vol.118
, pp. 1550-1573
-
-
Taylor, M.S.1
Jacobsen, E.N.2
-
72
-
-
33847782578
-
-
For the first example of using catalyst 3b to catalyze in situ generated imine, see
-
For the first example of using catalyst 3b to catalyze in situ generated imine, see: J. Song, H.-W. Shih, and L. Deng Org. Lett. 9 2007 603 606
-
(2007)
Org. Lett.
, vol.9
, pp. 603-606
-
-
Song, J.1
Shih, H.-W.2
Deng, L.3
-
75
-
-
11844302258
-
-
T. Okino, Y. Hoashi, T. Furukawa, X. Xu, and Y. Takemoto J. Am. Chem. Soc. 127 2005 119 125
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 119-125
-
-
Okino, T.1
Hoashi, Y.2
Furukawa, T.3
Xu, X.4
Takemoto, Y.5
-
76
-
-
84878751896
-
-
CCDC-896164 (4j) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
-
CCDC-896164 (4j) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
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-
-
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