-
1
-
-
84899749636
-
-
For an excellent book about the chemistry of pyrazol-3-ones: Pyrazol-3-ones. PartIV: (Ed.: A.R. Katritzky), Academic Press, 98
-
For an excellent book about the chemistry of pyrazol-3-ones: Pyrazol-3-ones. PartIV: Synthesis and Applications. G. Varvounis. Adv. Heterocyclic Chem. (Ed.: A.R. Katritzky), Academic Press, 2009, 98, 143.
-
(2009)
Synthesis and Applications. G. Varvounis. Adv. Heterocyclic Chem.
, pp. 143
-
-
-
4
-
-
84899750884
-
-
PCT Int.Appl. WO 46679
-
I. R. Matthews, PCT Int.Appl. WO 46679, 2005;
-
(2005)
-
-
Matthews, I.R.1
-
5
-
-
35348888465
-
-
A. Kimata, H. Nakagawa, R. Ohyama, T. Fukuuchi, S. Ohta, T. Suzuki, N. Miyata, J. Med. Chem. 2007, 50, 5053.
-
(2007)
J. Med. Chem.
, vol.50
, pp. 5053
-
-
Kimata, A.1
Nakagawa, H.2
Ohyama, R.3
Fukuuchi, T.4
Ohta, S.5
Suzuki, T.6
Miyata, N.7
-
6
-
-
77950362365
-
-
Y.-H. Liao, W.-B. Chen, Z.-J. Wu, X.-L. Du, L.-F. Cun, X.-M. Zhang, W.-C. Yuan, Adv. Synth. Catal. 2010, 352, 827.
-
(2010)
Adv. Synth. Catal.
, vol.352
, pp. 827
-
-
Liao, Y.-H.1
Chen, W.-B.2
Wu, Z.-J.3
Du, X.-L.4
Cun, L.-F.5
Zhang, X.-M.6
Yuan, W.-C.7
-
7
-
-
79951782547
-
-
A.-N. R. Alba, A. Zea, G. Valero, T. Calbet, M. Font-bardia, A. Mazzanti, A. Moyano, R. Rios, Eur. J. Org. Chem. 2011, 1318.
-
(2011)
Eur. J. Org. Chem.
, pp. 1318
-
-
Alba, A.-N.R.1
Zea, A.2
Valero, G.3
Calbet, T.4
Font-bardia, M.5
Mazzanti, A.6
Moyano, A.7
Rios, R.8
-
8
-
-
80052743131
-
-
A. Zea, A.-N. R. Alba, A. Mazzanti, A. Moyano, R. Rios, Org. Biomol. Chem. 2011, 9, 6519-6523.
-
(2011)
Org. Biomol. Chem.
, vol.9
, pp. 6519-6523
-
-
Zea, A.1
Alba, A.-N.R.2
Mazzanti, A.3
Moyano, A.4
Rios, R.5
-
9
-
-
84857214815
-
-
A. Mazzanti, T. Calbet, M. Font-Bardia, A. Moyano, R. Rios, Org. Biomol. Chem. 2012, 10, 1645-1652.
-
(2012)
Org. Biomol. Chem.
, vol.10
, pp. 1645-1652
-
-
Mazzanti, A.1
Calbet, T.2
Font-Bardia, M.3
Moyano, A.4
Rios, R.5
-
10
-
-
84899724165
-
-
For reviews on asymmetric α-amination reactions, see:
-
For reviews on asymmetric α-amination reactions, see:
-
-
-
-
13
-
-
22744432716
-
-
J. M. Janey, Angew. Chem. 2005, 117, 4364; Angew. Chem. Int. Ed. 2005, 44, 4292;
-
(2005)
Angew. Chem. 2005, 117, 4364; Angew. Chem. Int. Ed.
, vol.44
, pp. 4292
-
-
Janey, J.M.1
-
16
-
-
77649206387
-
-
For selected examples of asymmetric α-amination, see:
-
T. Vilaivan, W. Bhanthumnavin, Molecules 2010, 15, 917. For selected examples of asymmetric α-amination, see:
-
(2010)
Molecules
, vol.15
, pp. 917
-
-
Vilaivan, T.1
Bhanthumnavin, W.2
-
17
-
-
78650368798
-
-
T. Bui, G. Hernandez-Torres, C. Milite, C. F. Barbas III., Org. Lett. 2010, 12, 5696;
-
(2010)
Org. Lett.
, vol.12
, pp. 5696
-
-
Bui, T.1
Hernandez-Torres, G.2
Milite, C.3
Barbas III, C.F.4
-
18
-
-
78349261239
-
-
X. Han, F. Zhong, Y. Lu, Adv. Synth. Catal. 2010, 352, 778;
-
(2010)
Adv. Synth. Catal.
, vol.352
, pp. 778
-
-
Han, X.1
Zhong, F.2
Lu, Y.3
-
19
-
-
77950340760
-
-
S. Mouri, Z. Chen, H. Mitsunuma, M. Furutachi, S. Matsunaga, M. Shibasaki, J. Am. Chem. Soc. 2010, 132, 1255;
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 1255
-
-
Mouri, S.1
Chen, Z.2
Mitsunuma, H.3
Furutachi, M.4
Matsunaga, S.5
Shibasaki, M.6
-
20
-
-
77953175512
-
-
Z. G. Yang, Z. Wang, S. Bai, K. Shen, D. H. Chen, X. H. Liu, L. L. Lin, X. M. Feng, Chem. Eur. J. 2010, 16, 6632;
-
(2010)
Chem. Eur. J.
, vol.16
, pp. 6632
-
-
Yang, Z.G.1
Wang, Z.2
Bai, S.3
Shen, K.4
Chen, D.H.5
Liu, X.H.6
Lin, L.L.7
Feng, X.M.8
-
21
-
-
72249084937
-
-
T. Bui, M. Borrego, C. F. Barbas III., J. Org.Chem. 2009, 74, 8935;
-
(2009)
J. Org.Chem.
, vol.74
, pp. 8935
-
-
Bui, T.1
Borrego, M.2
Barbas III, C.F.3
-
22
-
-
70350043394
-
-
T. Mashiko, N. Kumagai, M. Shibasaki, J. Am. Chem. Soc. 2009, 131, 14990;
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 14990
-
-
Mashiko, T.1
Kumagai, N.2
Shibasaki, M.3
-
23
-
-
56749122183
-
-
R. He, X. Wang, T. Hashimoto, K. Maruoka, Angew. Chem. 2008, 120, 9608; Angew. Chem. Int. Ed. 2008, 47, 9466;
-
(2008)
Angew. Chem. 2008, 120, 9608; Angew. Chem. Int. Ed.
, vol.47
, pp. 9466
-
-
He, R.1
Wang, X.2
Hashimoto, T.3
Maruoka, K.4
-
24
-
-
34548537133
-
-
T.-Y. Liu, H. L. Cui, Y. Zhang, K. Jiang, W. Du, Z.-Q. He, Y.-C. Chen, Org. Lett. 2007, 9, 3671;
-
(2007)
Org. Lett.
, vol.9
, pp. 3671
-
-
Liu, T.-Y.1
Cui, H.L.2
Zhang, Y.3
Jiang, K.4
Du, W.5
He, Z.-Q.6
Chen, Y.-C.7
-
25
-
-
35048816162
-
-
T. Mashiko, K. Hara, D. Tanaka, Y. Fujiwara, N. Kumagai, M. Shibasaki, J. Am. Chem. Soc. 2007, 129, 11342.
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 11342
-
-
Mashiko, T.1
Hara, K.2
Tanaka, D.3
Fujiwara, Y.4
Kumagai, N.5
Shibasaki, M.6
-
26
-
-
84899762362
-
-
For selected examples see:
-
For selected examples see:
-
-
-
-
27
-
-
81555215435
-
-
F. Zhou, M. Ding, Y.-L. Liu, C.-H. Wang, C.-B. Ji, Y.-Y. Zhang, J. Zhou, Adv. Synth. Catal. 2011, 353, 2945;
-
(2011)
Adv. Synth. Catal.
, vol.353
, pp. 2945
-
-
Zhou, F.1
Ding, M.2
Liu, Y.-L.3
Wang, C.-H.4
Ji, C.-B.5
Zhang, Y.-Y.6
Zhou, J.7
-
28
-
-
0037024190
-
-
N. Kumaragurubaran, K. Juhl, W. Zhuang, A. Bøgevig, K. A. Jørgensen, J. Am. Chem. Soc. 2002, 124, 6254;
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 6254
-
-
Kumaragurubaran, N.1
Juhl, K.2
Zhuang, W.3
Bøgevig, A.4
Jørgensen, K.A.5
-
29
-
-
69449091605
-
-
L. Cheng, L. Liu, D. Wang, Y.-J. Che, Org. Lett. 2009, 11, 3874;
-
(2009)
Org. Lett.
, vol.11
, pp. 3874
-
-
Cheng, L.1
Liu, L.2
Wang, D.3
Che, Y.-J.4
-
31
-
-
79960848137
-
-
A. D'Esmanchelier, H. Yalgin, V. Coeffard, X. Moreau, C. Greck, Tetrahedron Lett. 2011, 52, 4430;
-
(2011)
Tetrahedron Lett.
, vol.52
, pp. 4430
-
-
D'Esmanchelier, A.1
Yalgin, H.2
Coeffard, V.3
Moreau, X.4
Greck, C.5
-
32
-
-
79957842272
-
-
J.-Y. Fu, Q.-C. Yang, Q.-L. Wang, J.-N. Ming, F.-Y. Wang, X.-Y. Xu, L.-X. Wang, J. Org. Chem. 2011, 76, 4661;
-
(2011)
J. Org. Chem.
, vol.76
, pp. 4661
-
-
Fu, J.-Y.1
Yang, Q.-C.2
Wang, Q.-L.3
Ming, J.-N.4
Wang, F.-Y.5
Xu, X.-Y.6
Wang, L.-X.7
-
33
-
-
79956089010
-
-
C. Liu, Q. Zhu, K.-W. Huang, Y. Lu, Org. Lett. 2011, 13, 2638.
-
(2011)
Org. Lett.
, vol.13
, pp. 2638
-
-
Liu, C.1
Zhu, Q.2
Huang, K.-W.3
Lu, Y.4
-
34
-
-
84899728121
-
-
For a non-exhaustive list of our previous works in organocatalysis see:
-
For a non-exhaustive list of our previous works in organocatalysis see:
-
-
-
-
35
-
-
52949138243
-
-
G. Valero, A.-N. Balaguer, A. Moyano, R. Rios, Tetrahedron Lett. 2008, 49, 6559;
-
(2008)
Tetrahedron Lett.
, vol.49
, pp. 6559
-
-
Valero, G.1
Balaguer, A.-N.2
Moyano, A.3
Rios, R.4
-
36
-
-
67650333224
-
-
X. Companyó, G. Valero, L. Crovetto, A. Moyano, R. Rios, Chem. Eur. J. 2009, 15, 6564;
-
(2009)
Chem. Eur. J.
, vol.15
, pp. 6564
-
-
Companyó, X.1
Valero, G.2
Crovetto, L.3
Moyano, A.4
Rios, R.5
-
37
-
-
67650252003
-
-
X. Companyó, M. Hejnová, M. Kamlar, J. Veselý, A. Moyano, R. Rios, Tetrahedron Lett. 2009, 50, 5021;
-
(2009)
Tetrahedron Lett.
, vol.50
, pp. 5021
-
-
Companyó, X.1
Hejnová, M.2
Kamlar, M.3
Veselý, J.4
Moyano, A.5
Rios, R.6
-
38
-
-
66749088008
-
-
X. Companyó, A.-N. Balaguer, F. Cárdenas, A. Moyano, R. Rios, Eur. J. Org. Chem. 2009, 3075;
-
(2009)
Eur. J. Org. Chem.
, pp. 3075
-
-
Companyó, X.1
Balaguer, A.-N.2
Cárdenas, F.3
Moyano, A.4
Rios, R.5
-
39
-
-
77951946549
-
-
A.-N. R. Alba, X. Companyó, G. Valero, A. Moyano, R. Rios, Chem. Eur. J. 2010, 16, 5354;
-
(2010)
Chem. Eur. J.
, vol.16
, pp. 5354
-
-
Alba, A.-N.R.1
Companyó, X.2
Valero, G.3
Moyano, A.4
Rios, R.5
-
40
-
-
77956458174
-
-
X. Companyó, A. Zea, A.-N. R. Alba, A. Mazzanti, A. Moyano, R. Rios, Chem. Commun. 2010, 46, 6953;
-
(2010)
Chem. Commun.
, vol.46
, pp. 6953
-
-
Companyó, X.1
Zea, A.2
Alba, A.-N.R.3
Mazzanti, A.4
Moyano, A.5
Rios, R.6
-
41
-
-
61749096057
-
-
G. Valero, J. Schimer, I. Císařová, J. Veselý, A. Moyano, R. Rios, Tetrahedron Lett. 2009, 50, 1943;
-
(2009)
Tetrahedron Lett.
, vol.50
, pp. 1943
-
-
Valero, G.1
Schimer, J.2
Císařová, I.3
Veselý, J.4
Moyano, A.5
Rios, R.6
-
42
-
-
80054006801
-
-
S. Číhalová, G. Valero, J. Schimer, M. Humpl, M. Dračínský, A. Moyano, R. Rios, J. Veselý, Tetrahedron 2011, 67, 8942-8950;
-
(2011)
Tetrahedron
, vol.67
, pp. 8942-8950
-
-
Číhalová, S.1
Valero, G.2
Schimer, J.3
Humpl, M.4
Dračínský, M.5
Moyano, A.6
Rios, R.7
Veselý, J.8
-
44
-
-
79951638031
-
-
For similar pyrazolone additions catalyzed by N-oxide metal complexes, see:
-
Z. Yang, Z. Wang, S. Bai, X. Liu, L. Lin, X. Feng, Org. Lett. 2011, 13, 596-599. For similar pyrazolone additions catalyzed by N-oxide metal complexes, see:
-
(2011)
Org. Lett.
, vol.13
, pp. 596-599
-
-
Yang, Z.1
Wang, Z.2
Bai, S.3
Liu, X.4
Lin, L.5
Feng, X.6
-
45
-
-
84863272254
-
-
Z. Wang, Z. Chen, S. Bai, W. Li, X. Liu, L. Lin, X. Feng, Angew. Chem. 2012, 124, 2830-2833; Angew. Chem. Int. Ed. 2012, 51, 2776-2779;
-
(2012)
Angew. Chem. 2012, 124, 2830-2833; Angew. Chem. Int. Ed.
, vol.51
, pp. 2776-2779
-
-
Wang, Z.1
Chen, Z.2
Bai, S.3
Li, W.4
Liu, X.5
Lin, L.6
Feng, X.7
-
46
-
-
79955767991
-
-
For an excellent review, see:
-
Z. Wang, Z. Yang, D. Chen, X. Liu, L. Lin, X. Feng, Angew. Chem. 2011, 123, 5030-5034; Angew. Chem. Int. Ed. 2011, 50, 4928-4932. For an excellent review, see:
-
(2011)
Angew. Chem. 2011, 123, 5030-5034; Angew. Chem. Int. Ed.
, vol.50
, pp. 4928-4932
-
-
Wang, Z.1
Yang, Z.2
Chen, D.3
Liu, X.4
Lin, L.5
Feng, X.6
-
47
-
-
80051741339
-
-
X. Liu, L. Lin, X. Feng, Acc. Chem. Res. 2011, 44, 574-587.
-
(2011)
Acc. Chem. Res.
, vol.44
, pp. 574-587
-
-
Liu, X.1
Lin, L.2
Feng, X.3
|