-
1
-
-
0037043180
-
-
B. List, Tetrahedron 2002, 58, 5573-5590
-
(2002)
Tetrahedron
, vol.58
, pp. 5573-5590
-
-
List, B.1
-
4
-
-
4143114533
-
-
W. Notz, F. Tanaka, C. F. Barbas III, Acc. Chem. Res. 2004, 37, 580-591
-
(2004)
Acc. Chem. Res.
, vol.37
, pp. 580-591
-
-
Notz, W.1
Tanaka, F.2
Barbas III, C.F.3
-
10
-
-
38349100690
-
-
S. Mukherjee, J. W. Yang, S. Hoffmann, B. List, Chem. Rev. 2007, 107, 5471-5569.
-
(2007)
Chem. Rev.
, vol.107
, pp. 5471-5569
-
-
Mukherjee, S.1
Yang, J.W.2
Hoffmann, S.3
List, B.4
-
11
-
-
0034654216
-
-
B. List, R. A. Lerner, C. F. Barbas III, J. Am. Chem. Soc. 2000, 122, 2395-2396.
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 2395-2396
-
-
List, B.1
Lerner, R.A.2
Barbas III, C.F.3
-
13
-
-
6044269452
-
-
Angew. Chem. Int. Ed. 2004, 43, 5138-5175
-
(2004)
Angew. Chem. Int. Ed.
, vol.43
, pp. 5138-5175
-
-
-
15
-
-
48849094479
-
-
Angew. Chem. Int. Ed. 2008, 47, 4638-4660.
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 4638-4660
-
-
-
16
-
-
0034600250
-
-
K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243-4324
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 4243-4324
-
-
Ahrendt, K.A.1
Borths, C.J.2
MacMillan, D.W.C.3
-
17
-
-
27544485685
-
-
Y. Huang, A. M. Walji, C. H. Larsen, D. W. C. MacMillan, J. Am. Chem. Soc. 2005, 127, 15051-15052
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 15051-15052
-
-
Huang, Y.1
Walji, A.M.2
Larsen, C.H.3
MacMillan, D.W.C.4
-
18
-
-
34247565955
-
-
T. D. Beeson, A. Mastracchio, J. Hong, K. Ashton, D. W. C. MacMillan, Science 2007, 316, 582-585.
-
(2007)
Science
, vol.316
, pp. 582-585
-
-
Beeson, T.D.1
Mastracchio, A.2
Hong, J.3
Ashton, K.4
MacMillan, D.W.C.5
-
19
-
-
78049495036
-
-
M. P. Patil, A. K. Sharma, R. B. Sunoj, J. Org. Chem. 2010, 75, 7310-7321.
-
(2010)
J. Org. Chem.
, vol.75
, pp. 7310-7321
-
-
Patil, M.P.1
Sharma, A.K.2
Sunoj, R.B.3
-
21
-
-
33845505476
-
-
For pioneering studies on diarylprolinol ethers, see
-
Angew. Chem. Int. Ed. 2006, 45, 7876-7880. For pioneering studies on diarylprolinol ethers, see
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 7876-7880
-
-
-
22
-
-
33645951837
-
-
Y. Hayashi, H. Gotoh, T. Hayasi, M. Shoji, Angew. Chem. 2005, 117, 4284-4287
-
(2005)
Angew. Chem.
, vol.117
, pp. 4284-4287
-
-
Hayashi, Y.1
Gotoh, H.2
Hayasi, T.3
Shoji, M.4
-
23
-
-
22144459070
-
-
Angew. Chem. Int. Ed. 2005, 44, 4212-4215
-
(2005)
Angew. Chem. Int. Ed.
, vol.44
, pp. 4212-4215
-
-
-
24
-
-
20444486476
-
-
M. Marigo, T. C. Wabnitz, D. Fielenbach, K. A. Jørgensen, Angew. Chem. 2005, 117, 804-807
-
(2005)
Angew. Chem.
, vol.117
, pp. 804-807
-
-
Marigo, M.1
Wabnitz, T.C.2
Fielenbach, D.3
Jørgensen, K.A.4
-
26
-
-
29844457732
-
-
J. Franzén, M. Marigo, D. Fielenbach, T. C. Wabnitz, A. Kjærsgaard, K. A. Jørgensen, J. Am. Chem. Soc. 2005, 127, 18296-18304.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 18296-18304
-
-
Franzén, J.1
Marigo, M.2
Fielenbach, D.3
Wabnitz, T.C.4
Kjærsgaard, A.5
Jørgensen, K.A.6
-
27
-
-
0242371514
-
-
M. Yamaguchi, T. Shiraishi, M. Hirama, Angew. Chem. 1993, 105, 1243-1245
-
(1993)
Angew. Chem.
, vol.105
, pp. 1243-1245
-
-
Yamaguchi, M.1
Shiraishi, T.2
Hirama, M.3
-
29
-
-
0343967492
-
-
M. Yamaguchi, T. Shiraishi, M. Hirama, J. Org. Chem. 1996, 61, 3520-3530.
-
(1996)
J. Org. Chem.
, vol.61
, pp. 3520-3530
-
-
Yamaguchi, M.1
Shiraishi, T.2
Hirama, M.3
-
30
-
-
24644518441
-
-
X. H. Liu, B. Qin, X. Zhou, B. He, X. M. Feng, J. Am. Chem. Soc. 2005, 127, 12224-12225.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 12224-12225
-
-
Liu, X.H.1
Qin, B.2
Zhou, X.3
He, B.4
Feng, X.M.5
-
31
-
-
80052865795
-
-
A. Karmakar, T. Maji, S. Wittmann, O. Reiser, Chem. Eur. J. 2011, 17, 11024-11029.
-
(2011)
Chem. Eur. J.
, vol.17
, pp. 11024-11029
-
-
Karmakar, A.1
Maji, T.2
Wittmann, S.3
Reiser, O.4
-
33
-
-
30044448417
-
-
R. Fernandez-Lopez, J. Kofoed, M. Machuqueiro, T. Darbre, Eur. J. Org. Chem. 2005, 5268-5276
-
(2005)
Eur. J. Org. Chem.
, pp. 5268-5276
-
-
Fernandez-Lopez, R.1
Kofoed, J.2
MacHuqueiro, M.3
Darbre, T.4
-
36
-
-
70349923605
-
-
For rubidium-proline-catalyzed asymmetric reactions, see: ref. [7]. For cobalt-proline-catalyzed asymmetric reaction, see: ref. [9]. For reactions catalyzed by primary amino acid metal salts, see
-
S. Itoh, M. Kitamura, Y. Yamada, S. Aoki, Chem. Eur. J. 2009, 15, 10570-10584. For rubidium-proline-catalyzed asymmetric reactions, see: ref. [7]. For cobalt-proline-catalyzed asymmetric reaction, see: ref. [9]. For reactions catalyzed by primary amino acid metal salts, see
-
(2009)
Chem. Eur. J.
, vol.15
, pp. 10570-10584
-
-
Itoh, S.1
Kitamura, M.2
Yamada, Y.3
Aoki, S.4
-
38
-
-
70449105089
-
-
M. Yoshida, M. Narita, K. Hirama, S. Hara, Tetrahedron Lett. 2009, 50, 7297-7299
-
(2009)
Tetrahedron Lett.
, vol.50
, pp. 7297-7299
-
-
Yoshida, M.1
Narita, M.2
Hirama, K.3
Hara, S.4
-
39
-
-
77953750714
-
-
M. Yoshida, A. Sato, S. Hara, Org. Biomol. Chem. 2010, 8, 3031-3036
-
(2010)
Org. Biomol. Chem.
, vol.8
, pp. 3031-3036
-
-
Yoshida, M.1
Sato, A.2
Hara, S.3
-
40
-
-
80054112865
-
-
M. Yoshida, K. Hirama, M. Narita, S. Hara, Symmetry 2011, 3, 155-164
-
(2011)
Symmetry
, vol.3
, pp. 155-164
-
-
Yoshida, M.1
Hirama, K.2
Narita, M.3
Hara, S.4
-
41
-
-
79953199027
-
-
M. Yoshida, N. Kitamikado, H. Ikehara, S. Hara, J. Org. Chem. 2011, 76, 2305-2309
-
(2011)
J. Org. Chem.
, vol.76
, pp. 2305-2309
-
-
Yoshida, M.1
Kitamikado, N.2
Ikehara, H.3
Hara, S.4
-
42
-
-
80054108505
-
-
M. Yoshida, M. Narita, S. Hara, J. Org. Chem. 2011, 76, 8513-8517
-
(2011)
J. Org. Chem.
, vol.76
, pp. 8513-8517
-
-
Yoshida, M.1
Narita, M.2
Hara, S.3
-
43
-
-
84862838203
-
-
M. Yoshida, E. Masaki, H. Ikehara, S. Hara, Org. Biomol. Chem. 2012, 10, 5289-5297.
-
(2012)
Org. Biomol. Chem.
, vol.10
, pp. 5289-5297
-
-
Yoshida, M.1
Masaki, E.2
Ikehara, H.3
Hara, S.4
-
44
-
-
0042590011
-
-
A. K. Peter, J. F. Liebman, L. C. Allen, J. Am. Chem. Soc. 1970, 92, 1142-1150
-
(1970)
J. Am. Chem. Soc.
, vol.92
, pp. 1142-1150
-
-
Peter, A.K.1
Liebman, J.F.2
Allen, L.C.3
-
47
-
-
0342854451
-
-
S. Salai, C. Ammal, P. Venuvanalingam, J. Phys. Chem. A 2000, 104, 10859-10867.
-
(2000)
J. Phys. Chem. A
, vol.104
, pp. 10859-10867
-
-
Salai, S.1
Ammal, C.2
Venuvanalingam, P.3
-
52
-
-
33847623075
-
-
D. Almasi, D. A. Alonso, C. Nájera, Tetrahedron: Asymmetry 2007, 18, 299-365.
-
(2007)
Tetrahedron: Asymmetry
, vol.18
, pp. 299-365
-
-
Almasi, D.1
Alonso, D.A.2
Nájera, C.3
-
53
-
-
38849183441
-
-
D. Enders, M. R. M. Hüttl, G. Raabe, J. W. Bats, Adv. Synth. Catal. 2008, 350, 267-279
-
(2008)
Adv. Synth. Catal.
, vol.350
, pp. 267-279
-
-
Enders, D.1
Hüttl, M.R.M.2
Raabe, G.3
Bats, J.W.4
-
54
-
-
80052478729
-
-
H. Ishikawa, S. Sawano, Y. Yasui, Y. Shibata, Y. Hayashi, Angew. Chem. 2011, 123, 3858-3863
-
(2011)
Angew. Chem.
, vol.123
, pp. 3858-3863
-
-
Ishikawa, H.1
Sawano, S.2
Yasui, Y.3
Shibata, Y.4
Hayashi, Y.5
-
55
-
-
79953709139
-
-
Angew. Chem. Int. Ed. 2011, 50, 3774-3779
-
(2011)
Angew. Chem. Int. Ed.
, vol.50
, pp. 3774-3779
-
-
-
56
-
-
79960201417
-
-
K. L. Jensen, G. Dickmeiss, B. S. Donslund, P. H. Poulsen, K. A. Jørgensen, Org. Lett. 2011, 13, 3678-3681.
-
(2011)
Org. Lett.
, vol.13
, pp. 3678-3681
-
-
Jensen, K.L.1
Dickmeiss, G.2
Donslund, B.S.3
Poulsen, P.H.4
Jørgensen, K.A.5
-
57
-
-
0035891780
-
-
For selected examples on the asymmetric Michael addition of ketones to nitro-olefins, see
-
J. M. Betancort, C. F. Barbas III, Org. Lett. 2001, 3, 3737-3740. For selected examples on the asymmetric Michael addition of ketones to nitro-olefins, see
-
(2001)
Org. Lett.
, vol.3
, pp. 3737-3740
-
-
Betancort, J.M.1
Barbas III, C.F.2
-
58
-
-
3543065878
-
-
T. Ishii, S. Fujioka, Y. Sekiguchi, H. Kotsuki, J. Am. Chem. Soc. 2004, 126, 9558-9559
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 9558-9559
-
-
Ishii, T.1
Fujioka, S.2
Sekiguchi, Y.3
Kotsuki, H.4
-
59
-
-
33646142092
-
-
N. Mase, K. Watanabe, H. Yoda, K. Takabe, F. Tanaka, C. F. Barbas III, J. Am. Chem. Soc. 2006, 128, 4966-4967
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 4966-4967
-
-
Mase, N.1
Watanabe, K.2
Yoda, H.3
Takabe, K.4
Tanaka, F.5
Barbas III, C.F.6
-
60
-
-
33645909878
-
-
Y. Xu, W. Zou, H. Sunden, I. Ibrahem, A. Córdova, Adv. Synth. Catal. 2006, 348, 418-424
-
(2006)
Adv. Synth. Catal.
, vol.348
, pp. 418-424
-
-
Xu, Y.1
Zou, W.2
Sunden, H.3
Ibrahem, I.4
Córdova, A.5
-
64
-
-
64349100404
-
-
For selected example on asymmetric Michael addition of ketoesters to nitro-olefins, see
-
B. Ni, Q. Zhang, K. Dhungana, A. D. Headley, Org. Lett. 2009, 11, 1037-1040. For selected example on asymmetric Michael addition of ketoesters to nitro-olefins, see
-
(2009)
Org. Lett.
, vol.11
, pp. 1037-1040
-
-
Ni, B.1
Zhang, Q.2
Dhungana, K.3
Headley, A.D.4
-
65
-
-
77950262715
-
-
A. Nakamura, S. Lectard, D. Hashizume, Y. Hamashima, M. Sodeoka, J. Am. Chem. Soc. 2010, 132, 4036-4037.
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 4036-4037
-
-
Nakamura, A.1
Lectard, S.2
Hashizume, D.3
Hamashima, Y.4
Sodeoka, M.5
-
67
-
-
53849091017
-
-
A. Quintard, C. Bournaud, A. Alexakis, Chem. Eur. J. 2008, 14, 7504-7507
-
(2008)
Chem. Eur. J.
, vol.14
, pp. 7504-7507
-
-
Quintard, A.1
Bournaud, C.2
Alexakis, A.3
-
68
-
-
81755187358
-
-
A. Quintard, J. B. Langlois, D. Emery, J. Mareda, L. Guéné e, A. Alexakis, Chem. Eur. J. 2011, 17, 13433-13437.
-
(2011)
Chem. Eur. J.
, vol.17
, pp. 13433-13437
-
-
Quintard, A.1
Langlois, J.B.2
Emery, D.3
Mareda, J.4
Guénée, L.5
Alexakis, A.6
-
69
-
-
22144469096
-
-
W. Wang, J. Wang, H. Li, Angew. Chem. 2005, 117, 1393-1395
-
(2005)
Angew. Chem.
, vol.117
, pp. 1393-1395
-
-
Wang, W.1
Wang, J.2
Li, H.3
-
70
-
-
14844316261
-
-
Angew. Chem. Int. Ed. 2005, 44, 1369-1371
-
(2005)
Angew. Chem. Int. Ed.
, vol.44
, pp. 1369-1371
-
-
-
71
-
-
33744808244
-
-
J. Wang, H. Li, L. S. Zu, H. Gao, W. Wang, Chem. Eur. J. 2006, 12, 4321-4332.
-
(2006)
Chem. Eur. J.
, vol.12
, pp. 4321-4332
-
-
Wang, J.1
Li, H.2
Zu, L.S.3
Gao, H.4
Wang, W.5
-
72
-
-
34250803515
-
-
C. Palomo, S. Vera, A. Mielgo, E. Gómez-Bengoa, Angew. Chem. 2006, 118, 6130-6133
-
(2006)
Angew. Chem.
, vol.118
, pp. 6130-6133
-
-
Palomo, C.1
Vera, S.2
Mielgo, A.3
Gómez-Bengoa, E.4
-
73
-
-
33748791724
-
-
Angew. Chem. Int. Ed. 2006, 45, 5984-5987.
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 5984-5987
-
-
-
74
-
-
34250619640
-
-
M. P. Lalonde, Y. Chen, E. N. Jacobsen, Angew. Chem. 2006, 118, 6514-6518
-
(2006)
Angew. Chem.
, vol.118
, pp. 6514-6518
-
-
Lalonde, M.P.1
Chen, Y.2
Jacobsen, E.N.3
-
75
-
-
33749340635
-
-
Angew. Chem. Int. Ed. 2006, 45, 6366-6370.
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 6366-6370
-
-
-
76
-
-
70349292429
-
-
R. J. Reddy, H. H. Kuan, T. Y. Chou, K. Chen, Chem. Eur. J. 2009, 15, 9294-9298
-
(2009)
Chem. Eur. J.
, vol.15
, pp. 9294-9298
-
-
Reddy, R.J.1
Kuan, H.H.2
Chou, T.Y.3
Chen, K.4
-
77
-
-
77953563112
-
-
Y. F. Ting, C. Chang, R. J. Reddy, D. R. Magar, K. Chen, Chem. Eur. J. 2010, 16, 7030-7038.
-
(2010)
Chem. Eur. J.
, vol.16
, pp. 7030-7038
-
-
Ting, Y.F.1
Chang, C.2
Reddy, R.J.3
Magar, D.R.4
Chen, K.5
-
78
-
-
77949780968
-
-
J. Xiao, F. X. Xu, Y. P. Lu, T. P. Loh, Org. Lett. 2010, 12, 1220-1223.
-
(2010)
Org. Lett.
, vol.12
, pp. 1220-1223
-
-
Xiao, J.1
Xu, F.X.2
Lu, Y.P.3
Loh, T.P.4
-
80
-
-
0034812506
-
-
K. Sakthivel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260-5267
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 5260-5267
-
-
Sakthivel, K.1
Notz, W.2
Bui, T.3
Barbas III, C.F.4
-
81
-
-
0000761777
-
-
B. List, P. Pojarliev, H. Martin, Org. Lett. 2001, 3, 2423-2425
-
(2001)
Org. Lett.
, vol.3
, pp. 2423-2425
-
-
List, B.1
Pojarliev, P.2
Martin, H.3
-
82
-
-
0036138062
-
-
For Michael additions of aldehydes to nitro-olefins catalyzed by the combination of proline and additives, see
-
D. Enders, A. Seki, Synlett 2002, 26-28. For Michael additions of aldehydes to nitro-olefins catalyzed by the combination of proline and additives, see
-
(2002)
Synlett
, pp. 26-28
-
-
Enders, D.1
Seki, A.2
-
83
-
-
33846946866
-
-
B. M. Choudary, Ch. V. Rajasekhar, G. G. Krishna, K. R. Reddy, Synth. Commun. 2007, 37, 91-98
-
(2007)
Synth. Commun.
, vol.37
, pp. 91-98
-
-
Choudary, B.M.1
Rajasekhar, Ch.V.2
Krishna, G.G.3
Reddy, K.R.4
-
85
-
-
54749140370
-
-
Angew. Chem. Int. Ed. 2008, 47, 7714-7717
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 7714-7717
-
-
-
87
-
-
78951476535
-
-
For Michael additions with α-branched aldehydes as donors catalyzed by amino acid metal salts, see: refs. [10f, h]. For selected examples of silylated pyrrolidine catalysts, see
-
W. H. Wang, T. Abe, X. B. Wang, K. Kodama, T. Hirose, G. Y. Zhang, Tetrahedron: Asymmetry 2010, 21, 2925-2933. For Michael additions with α-branched aldehydes as donors catalyzed by amino acid metal salts, see: refs. [10f, h]. For selected examples of silylated pyrrolidine catalysts, see
-
(2010)
Tetrahedron: Asymmetry
, vol.21
, pp. 2925-2933
-
-
Wang, W.H.1
Abe, T.2
Wang, X.B.3
Kodama, K.4
Hirose, T.5
Zhang, G.Y.6
-
88
-
-
78249284338
-
-
R. Husmann, M. Jörres, G. Raabe, C. Bolm, Chem. Eur. J. 2010, 16, 12549-12552
-
(2010)
Chem. Eur. J.
, vol.16
, pp. 12549-12552
-
-
Husmann, R.1
Jörres, M.2
Raabe, G.3
Bolm, C.4
-
89
-
-
78249271709
-
-
J. O. Bauer, J. Stiller, E. Marqués-López, K. Strohfeldt, M. Christmann, C. Strohmann, Chem. Eur. J. 2010, 16, 12553-12558
-
(2010)
Chem. Eur. J.
, vol.16
, pp. 12553-12558
-
-
Bauer, J.O.1
Stiller, J.2
Marqués-López, E.3
Strohfeldt, K.4
Christmann, M.5
Strohmann, C.6
-
90
-
-
80052159472
-
-
K. I. Jentzsch, T. Min, J. I. Etcheson, J. C. Fettinger, A. K. Franz, J. Org. Chem. 2011, 76, 7065-7075.
-
(2011)
J. Org. Chem.
, vol.76
, pp. 7065-7075
-
-
Jentzsch, K.I.1
Min, T.2
Etcheson, J.I.3
Fettinger, J.C.4
Franz, A.K.5
-
91
-
-
33846126231
-
-
E. Reyes, J. L. Vicario, D. Badía, L. Carrillo, Org. Lett. 2006, 8, 6135-6138
-
(2006)
Org. Lett.
, vol.8
, pp. 6135-6138
-
-
Reyes, E.1
Vicario, J.L.2
Badía, D.3
Carrillo, L.4
-
93
-
-
54849157400
-
-
P. García-García, A. Ladépêche, R. Halder, B. List, Angew. Chem. 2008, 120, 4797-4799
-
(2008)
Angew. Chem.
, vol.120
, pp. 4797-4799
-
-
García-García, P.1
Ladépêche, A.2
Halder, R.3
List, B.4
-
94
-
-
48749133072
-
-
Angew. Chem. Int. Ed. 2008, 47, 4719-4721
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 4719-4721
-
-
-
95
-
-
61349116782
-
-
D. Bonne, L. Salat, J. P. Dulcère, J. Rodriguez, Org. Lett. 2008, 10, 5409-5412
-
(2008)
Org. Lett.
, vol.10
, pp. 5409-5412
-
-
Bonne, D.1
Salat, L.2
Dulcère, J.P.3
Rodriguez, J.4
-
96
-
-
55049091486
-
-
F. Xue, S. L. Zhang, W. H. Duan, W. Wang, Adv. Synth. Catal. 2008, 350, 2194-2198
-
(2008)
Adv. Synth. Catal.
, vol.350
, pp. 2194-2198
-
-
Xue, F.1
Zhang, S.L.2
Duan, W.H.3
Wang, W.4
-
98
-
-
62949181205
-
-
X. J. Zhang, S. P. Liu, X. M. Li, M. Yan, A. S. C. Chan, Chem. Commun. 2009, 833-835
-
(2009)
Chem. Commun.
, pp. 833-835
-
-
Zhang, X.J.1
Liu, S.P.2
Li, X.M.3
Yan, M.4
Chan, A.S.C.5
-
99
-
-
70349898269
-
-
B. Han, Y. C. Xiao, Z. Q. He, Y. C. Chen, Org. Lett. 2009, 11, 4660-4663.
-
(2009)
Org. Lett.
, vol.11
, pp. 4660-4663
-
-
Han, B.1
Xiao, Y.C.2
He, Z.Q.3
Chen, Y.C.4
-
100
-
-
47749137879
-
-
M. Gruttadauria, F. Giacalone, R. Noto, Chem. Soc. Rev. 2008, 37, 1666-1688
-
(2008)
Chem. Soc. Rev.
, vol.37
, pp. 1666-1688
-
-
Gruttadauria, M.1
Giacalone, F.2
Noto, R.3
-
101
-
-
64549151421
-
-
A. F. Trindade, P. M. P. Gois, C. A. M. Afonso, Chem. Rev. 2009, 109, 418-514
-
(2009)
Chem. Rev.
, vol.109
, pp. 418-514
-
-
Trindade, A.F.1
Gois, P.M.P.2
Afonso, C.A.M.3
-
102
-
-
78249263710
-
-
S. Shylesh, V. Schünemann, W. R. Thiel, Angew. Chem. 2010, 122, 3504-3537
-
(2010)
Angew. Chem.
, vol.122
, pp. 3504-3537
-
-
Shylesh, S.1
Schünemann, V.2
Thiel, W.R.3
-
103
-
-
77952409644
-
-
Angew. Chem. Int. Ed. 2010, 49, 3428-3459.
-
(2010)
Angew. Chem. Int. Ed.
, vol.49
, pp. 3428-3459
-
-
-
104
-
-
74849117325
-
-
M. Wiesner, G. Upert, G. Angelici, H. Wennemers, J. Am. Chem. Soc. 2010, 132, 6-7.
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 6-7
-
-
Wiesner, M.1
Upert, G.2
Angelici, G.3
Wennemers, H.4
-
105
-
-
74849103683
-
-
Z. L. Zheng, B. L. Perkins, B. K. Ni, J. Am. Chem. Soc. 2010, 132, 50-51.
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 50-51
-
-
Zheng, Z.L.1
Perkins, B.L.2
Ni, B.K.3
-
106
-
-
84861535832
-
-
C. A. Wang, Z. K. Zhang, T. Y. Y. L. Sun, L. Wang, W. D. Wang, Y. Zhang, C. Liu, W. Wang, Chem. Eur. J. 2012, 18, 6718-6723.
-
(2012)
Chem. Eur. J.
, vol.18
, pp. 6718-6723
-
-
Wang, C.A.1
Zhang, Z.K.2
Sun, T.Y.Y.L.3
Wang, L.4
Wang, W.D.5
Zhang, Y.6
Liu, C.7
Wang, W.8
-
107
-
-
84866392804
-
-
K. Xu, G. Y. Lai, Z. G. Zha, S. S. Pan, H. W. Chen, Z. Y. Wang, Chem. Eur. J. 2012, 18, 12357-12362.
-
(2012)
Chem. Eur. J.
, vol.18
, pp. 12357-12362
-
-
Xu, K.1
Lai, G.Y.2
Zha, Z.G.3
Pan, S.S.4
Chen, H.W.5
Wang, Z.Y.6
-
108
-
-
84866362705
-
-
MS (EESI) analysis was developed by the Chen group; for selected example, see
-
MS (EESI) analysis was developed by the Chen group; for selected example, see:, H. W. Chen, S. P. Yang, M. Li, B. Hu, J. Q. Li, J. Wang, Angew. Chem. 2010, 122, 3117-3120
-
(2010)
Angew. Chem.
, vol.122
, pp. 3117-3120
-
-
Chen, H.W.1
Yang, S.P.2
Li, M.3
Hu, B.4
Li, J.Q.5
Wang, J.6
-
109
-
-
77951202946
-
-
Angew. Chem. Int. Ed. 2010, 49, 3053-3056.
-
(2010)
Angew. Chem. Int. Ed.
, vol.49
, pp. 3053-3056
-
-
-
110
-
-
77953516053
-
-
C. Laurence, J. Graton, M. Berthelot, F. Besseau, J. Y. Le Questel, M. Luçon, C. Ouvrard, A. Planchat, E. Renault, J. Org. Chem. 2010, 75, 4105-4123.
-
(2010)
J. Org. Chem.
, vol.75
, pp. 4105-4123
-
-
Laurence, C.1
Graton, J.2
Berthelot, M.3
Besseau, F.4
Le Questel, J.Y.5
Luçon, M.6
Ouvrard, C.7
Planchat, A.8
Renault, E.9
-
111
-
-
33746322013
-
-
The nitro group could be activated by multiple hydrogen-bonding interactions, see: refs. [18, 22g]. For a review on hydrogen bonding, see
-
The nitro group could be activated by multiple hydrogen-bonding interactions, see: refs. [18, 22g]. For a review on hydrogen bonding, see:, M. S. Taylor, E. N. Jacobsen, Angew. Chem. 2006, 118, 1550-1573
-
(2006)
Angew. Chem.
, vol.118
, pp. 1550-1573
-
-
Taylor, M.S.1
Jacobsen, E.N.2
-
112
-
-
33646468489
-
-
Angew. Chem. Int. Ed. 2006, 45, 1520-1543.
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 1520-1543
-
-
-
113
-
-
0025352932
-
-
S. Fushiya, S. Sato, T. Kanazawa, G. Kusano, S. Nozoe, Tetrahedron Lett. 1990, 31, 3901-3904
-
(1990)
Tetrahedron Lett.
, vol.31
, pp. 3901-3904
-
-
Fushiya, S.1
Sato, S.2
Kanazawa, T.3
Kusano, G.4
Nozoe, S.5
-
115
-
-
79952147387
-
-
T. Higashi, Y. Isobe, H. Ouchi, H. Suzuki, Y. Okazaki, T. Asakawa, T. Furuta, T. Wakimoto, T. Kan, Org. Lett. 2011, 13, 1089-1091.
-
(2011)
Org. Lett.
, vol.13
, pp. 1089-1091
-
-
Higashi, T.1
Isobe, Y.2
Ouchi, H.3
Suzuki, H.4
Okazaki, Y.5
Asakawa, T.6
Furuta, T.7
Wakimoto, T.8
Kan, T.9
-
117
-
-
82455190988
-
-
J. Stöckigt, A. P. Antonchick, F. R. Wu, H. Waldmann, Angew. Chem. 2011, 123, 8692-8719
-
(2011)
Angew. Chem.
, vol.123
, pp. 8692-8719
-
-
Stöckigt, J.1
Antonchick, A.P.2
Wu, F.R.3
Waldmann, H.4
-
118
-
-
80052483777
-
-
Angew. Chem. Int. Ed. 2011, 50, 8538-8564.
-
(2011)
Angew. Chem. Int. Ed.
, vol.50
, pp. 8538-8564
-
-
-
119
-
-
84874627058
-
-
CCDC-888079 (8 a) 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.
-
-
-
|