-
7
-
-
22144459070
-
-
Y. Hayashi, T. Gotoh, T. Hayasji, and M. Shoji Angew. Chem., Int. Ed. 44 2005 4212
-
(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 4212
-
-
Hayashi, Y.1
Gotoh, T.2
Hayasji, T.3
Shoji, M.4
-
13
-
-
11844302258
-
-
T. Okino, Y. Hoashi, T. Furukawa, X. Xu, and Y. Takemoto J. Am. Chem. Soc. 127 2005 119
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 119
-
-
Okino, T.1
Hoashi, Y.2
Furukawa, T.3
Xu, X.4
Takemoto, Y.5
-
15
-
-
11244281650
-
-
For selected example, see: H. Li, Y. Wang, L. Tang, F. Wu, X. Liu, C. Guo, B.M. Foxman, and L. Deng Angew. Chem., Int. Ed. 44 2005 105
-
(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 105
-
-
Li, H.1
Wang, Y.2
Tang, L.3
Wu, F.4
Liu, X.5
Guo, C.6
Foxman, B.M.7
Deng, L.8
-
16
-
-
27144522622
-
-
For selected examples, see: J. Wang, H. Li, W. Duan, L. Zu, and W. Wang Org. Lett. 7 2005 4713
-
(2005)
Org. Lett.
, vol.7
, pp. 4713
-
-
Wang, J.1
Li, H.2
Duan, W.3
Zu, L.4
Wang, W.5
-
17
-
-
46849103420
-
-
F.-Z. Peng, Z.-H. Shao, B.-M. Fan, H. Song, G.-P. Li, and H.-B. Zhang J. Org. Chem. 73 2008 5202
-
(2008)
J. Org. Chem.
, vol.73
, pp. 5202
-
-
Peng, F.-Z.1
Shao, Z.-H.2
Fan, B.-M.3
Song, H.4
Li, G.-P.5
Zhang, H.-B.6
-
18
-
-
53849087875
-
-
P. Gao, C. Wang, Y. Wu, Z. Zhou, and C. Tang Eur. J. Org. Chem. 2008 4563
-
(2008)
Eur. J. Org. Chem.
, pp. 4563
-
-
Gao, P.1
Wang, C.2
Wu, Y.3
Zhou, Z.4
Tang, C.5
-
19
-
-
33750357708
-
-
For some key examples about the application of anthrone in some enantioselective reactions, see: J. Shen, T.T. Nguyen, Y.-P. Goh, W. Ye, X. Fu, J. Xu, and C.-H. Tan J. Am. Chem. Soc. 128 2006 13692
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 13692
-
-
Shen, J.1
Nguyen, T.T.2
Goh, Y.-P.3
Ye, W.4
Fu, X.5
Xu, J.6
Tan, C.-H.7
-
23
-
-
0031036734
-
-
K. Tokioka, S. Masuda, T. Fujii, Y. Hata, and Y. Yamamoto Tetrahedron: Asymmetry 8 1997 101
-
(1997)
Tetrahedron: Asymmetry
, vol.8
, pp. 101
-
-
Tokioka, K.1
Masuda, S.2
Fujii, T.3
Hata, Y.4
Yamamoto, Y.5
-
24
-
-
77954584491
-
-
C. Wu, W. Li, J. Yang, X. Liang, and J. Ye Org. Biomol. Chem. 8 2010 3244
-
(2010)
Org. Biomol. Chem.
, vol.8
, pp. 3244
-
-
Wu, C.1
Li, W.2
Yang, J.3
Liang, X.4
Ye, J.5
-
25
-
-
77952189791
-
-
A. Zea, G. Valero, A.N.R. Alba, A. Moyano, and R. Rios Adv. Synth. Catal. 352 2010 1102
-
(2010)
Adv. Synth. Catal.
, vol.352
, pp. 1102
-
-
Zea, A.1
Valero, G.2
Alba, A.N.R.3
Moyano, A.4
Rios, R.5
-
26
-
-
71849085618
-
-
For the examples of asymmetric Michael addition of anthrone to nitroalkenes, see: Y.-H. Liao, H. Zhang, Z.-J. Wu, L.-F. Cun, X.-M. Zhang, and W.-C. Yuan Tetrahedron: Asymmetry 20 2009 2397
-
(2009)
Tetrahedron: Asymmetry
, vol.20
, pp. 2397
-
-
Liao, Y.-H.1
Zhang, H.2
Wu, Z.-J.3
Cun, L.-F.4
Zhang, X.-M.5
Yuan, W.-C.6
-
28
-
-
34250613134
-
-
For selected reviews of Michael addition with various electrophiles, see: S.B. Tsogoeva Eur. J. Org. Chem. 2007 1701
-
(2007)
Eur. J. Org. Chem.
, pp. 1701
-
-
Tsogoeva, S.B.1
-
30
-
-
72949097675
-
-
To date, only a few examples concern about the Michael addition reaction with 3-methyl-4-nitro-5-alkenyl-isoxazoles as electrophiles, see: A. Baschieri, L. Bernardi, A. Ricci, S. Suresh, and M.F.A. Adamo Angew. Chem., Int. Ed. 48 2009 9342
-
(2009)
Angew. Chem., Int. Ed.
, vol.48
, pp. 9342
-
-
Baschieri, A.1
Bernardi, L.2
Ricci, A.3
Suresh, S.4
Adamo, M.F.A.5
-
38
-
-
0021882391
-
-
J. DiGiovanni, P.C. Decina, W.P. Pritchett, J. Cantor, K.K. Aalfs, and M.M. Coombs Cancer Res. 45 1985 2584
-
(1985)
Cancer Res.
, vol.45
, pp. 2584
-
-
Digiovanni, J.1
Decina, P.C.2
Pritchett, W.P.3
Cantor, J.4
Aalfs, K.K.5
Coombs, M.M.6
-
39
-
-
72149133668
-
-
K. Srinivas, K. Yesudas, K. Bhanuprakash, J.V. Rao, and L. Giribabu J. Phys. Chem. C 113 2009 20117
-
(2009)
J. Phys. Chem. C
, vol.113
, pp. 20117
-
-
Srinivas, K.1
Yesudas, K.2
Bhanuprakash, K.3
Rao, J.V.4
Giribabu, L.5
-
43
-
-
47549096279
-
-
H.-S. Huang, J.-F. Chiou, H.-F. Chiu, R.-F. Chen, and Y.-L. Lai Arch. Pharm. 335 2002 33
-
(2002)
Arch. Pharm.
, vol.335
, pp. 33
-
-
Huang, H.-S.1
Chiou, J.-F.2
Chiu, H.-F.3
Chen, R.-F.4
Lai, Y.-L.5
-
44
-
-
0034903402
-
-
H.-S. Huang, J.-M. Hwang, Y.-M. Jen, J.-J. Lin, K.-Y. Lee, C.-H. Shi, and H.-C. Hsu Chem. Pharm. Bull. 49 2001 969
-
(2001)
Chem. Pharm. Bull.
, vol.49
, pp. 969
-
-
Huang, H.-S.1
Hwang, J.-M.2
Jen, Y.-M.3
Lin, J.-J.4
Lee, K.-Y.5
Shi, C.-H.6
Hsu, H.-C.7
-
45
-
-
0038155176
-
-
H. Prinz, Y. Ishii, T. Hirano, T. Stoiber, J.A. Camacho Gómez, F. Schmidt, H. Düssmann, A.M. Burger, J.H.M. Prehn, E.G. Günter, and K. Umezawa J. Med. Chem. 46 2003 3382
-
(2003)
J. Med. Chem.
, vol.46
, pp. 3382
-
-
Prinz, H.1
Ishii, Y.2
Hirano, T.3
Stoiber, T.4
Camacho Gómez, J.A.5
Schmidt, F.6
Düssmann, H.7
Burger, A.M.8
Prehn, J.H.M.9
Günter, E.G.10
Umezawa, K.11
-
55
-
-
74049114934
-
-
W.-B. Chen, X.-L. Du, L.-F. Cun, X.-M. Zhang, and W.-C. Yuan Tetrahedron 66 2010 1441
-
(2010)
Tetrahedron
, vol.66
, pp. 1441
-
-
Chen, W.-B.1
Du, X.-L.2
Cun, L.-F.3
Zhang, X.-M.4
Yuan, W.-C.5
-
56
-
-
77950362365
-
-
Y.-H. Liao, W.-B. Chen, Z.-J. Wu, X.-L. Du, L.-F. Cun, X.-M. Zhang, and W.-C. Yuan Adv. Synth. Catal 352 2010 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
-
58
-
-
77954560523
-
-
W.-B. Chen, Z.-J. Wu, Q.-L. Pei, L.-F. Cun, X.-M. Zhang, and W.-C. Yuan Org. Lett. 12 2010 3132
-
(2010)
Org. Lett.
, vol.12
, pp. 3132
-
-
Chen, W.-B.1
Wu, Z.-J.2
Pei, Q.-L.3
Cun, L.-F.4
Zhang, X.-M.5
Yuan, W.-C.6
-
59
-
-
77954111282
-
-
Y.-H. Liao, X.-L. Liu, Z.-J. Wu, L.-F. Cun, X.-M. Zhang, and W.-C. Yuan Org. Lett. 12 2010 2896
-
(2010)
Org. Lett.
, vol.12
, pp. 2896
-
-
Liao, Y.-H.1
Liu, X.-L.2
Wu, Z.-J.3
Cun, L.-F.4
Zhang, X.-M.5
Yuan, W.-C.6
-
60
-
-
77954543828
-
-
X.-L. Liu, Y.-H. Liao, Z.-J. Wu, L.-F. Cun, X.-M. Zhang, and W.-C. Yuan J. Org. Chem. 75 2010 4872
-
(2010)
J. Org. Chem.
, vol.75
, pp. 4872
-
-
Liu, X.-L.1
Liao, Y.-H.2
Wu, Z.-J.3
Cun, L.-F.4
Zhang, X.-M.5
Yuan, W.-C.6
-
61
-
-
34547736906
-
-
As for the 3-methyl-4-nitro-5-alkenyl-isoxazoles substrates used in this work, only the E isomers can be obtained from 3,5-dimethyl-4-nitroisoxazole with various aromatic, heteroaromatic or aliphatic aldehydes according to the procedures reported by Adamo and co-workers. For details, see: M.F.A. Adamo, E.F. Duffy, V.R. Konda, and F. Murphy Heterocycles 71 2007 1173
-
(2007)
Heterocycles
, vol.71
, pp. 1173
-
-
Adamo, M.F.A.1
Duffy, E.F.2
Konda, V.R.3
Murphy, F.4
-
63
-
-
15444366940
-
-
For selected examples about the application of chiral bifunctional thiourea-tertiary amine in catalytic asymmetric transformations, see: B.-J. Li, L. Jiang, M. Liu, Y.-C. Chen, L.-S. Ding, and Y. Wu Synlett 2005 603
-
(2005)
Synlett
, pp. 603
-
-
Li, B.-J.1
Jiang, L.2
Liu, M.3
Chen, Y.-C.4
Ding, L.-S.5
Wu, Y.6
-
65
-
-
13444270903
-
-
A. Berkessel, F. Cleemann, S. Mukherjee, T.N. Müller, and J. Lex Angew. Chem., Int. Ed 44 2005 807
-
(2005)
Angew. Chem., Int. Ed
, vol.44
, pp. 807
-
-
Berkessel, A.1
Cleemann, F.2
Mukherjee, S.3
Müller, T.N.4
Lex, J.5
-
66
-
-
17444385209
-
-
A. Berkessel, S. Mukherjee, F. Cleemann, T.N. Müller, and J. Lex Chem. Commun. 2005 1898
-
(2005)
Chem. Commun.
, pp. 1898
-
-
Berkessel, A.1
Mukherjee, S.2
Cleemann, F.3
Müller, T.N.4
Lex, J.5
-
69
-
-
25444432564
-
-
J. Wang, H. Li, X. Yu, L. Zu, and W. Wang Org. Lett. 7 2005 4293
-
(2005)
Org. Lett.
, vol.7
, pp. 4293
-
-
Wang, J.1
Li, H.2
Yu, X.3
Zu, L.4
Wang, W.5
-
70
-
-
24944473938
-
-
T. Honjo, S. Sano, M. Shiro, and Y. Nagao Angew. Chem., Int. Ed. 44 2005 5838
-
(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 5838
-
-
Honjo, T.1
Sano, S.2
Shiro, M.3
Nagao, Y.4
-
71
-
-
27144518078
-
-
R.P. Herrera, V. Sgarzani, L. Bernardi, and A. Ricci Angew. Chem., Int. Ed. 44 2005 6576
-
(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 6576
-
-
Herrera, R.P.1
Sgarzani, V.2
Bernardi, L.3
Ricci, A.4
|