-
1
-
-
43749115932
-
-
For a recent review of chroman derivatives with biological activity, see: G.X. Wang, N.X. Wang, T. Shi, J.L. Yu, and X.L. Tang Prog. Chem. 20 2008 518
-
(2008)
Prog. Chem.
, vol.20
, pp. 518
-
-
Wang, G.X.1
Wang, N.X.2
Shi, T.3
Yu, J.L.4
Tang, X.L.5
-
2
-
-
77953205188
-
-
J.H. Kwak, H.E. Kang, J.K. Jung, H. Kim, J. Cho, and H. Lee Arch. Pharm. Res. 29 2006 934
-
(2006)
Arch. Pharm. Res.
, vol.29
, pp. 934
-
-
Kwak, J.H.1
Kang, H.E.2
Jung, J.K.3
Kim, H.4
Cho, J.5
Lee, H.6
-
3
-
-
33646808949
-
-
Y. Kanbe, M.H. Kim, M. Nishimoto, Y. Ohtake, N. Kato, T. Tsunenari, K. Taniguchi, I. Ohizumi, S. Kaiho, K. Morikawa, J.C. Jo, H.S. Lim, and H.Y. Kim Bioorg. Med. Chem. 14 2006 4803
-
(2006)
Bioorg. Med. Chem.
, vol.14
, pp. 4803
-
-
Kanbe, Y.1
Kim, M.H.2
Nishimoto, M.3
Ohtake, Y.4
Kato, N.5
Tsunenari, T.6
Taniguchi, K.7
Ohizumi, I.8
Kaiho, S.9
Morikawa, K.10
Jo, J.C.11
Lim, H.S.12
Kim, H.Y.13
-
6
-
-
0023875442
-
-
L.D. Wise, H.A. Dewald, E.S. Hawkins, D.M. Reynolds, T.G. Heffner, L.T. Meltzer, and T.A. Pugsley J. Med. Chem. 31 1988 688
-
(1988)
J. Med. Chem.
, vol.31
, pp. 688
-
-
Wise, L.D.1
Dewald, H.A.2
Hawkins, E.S.3
Reynolds, D.M.4
Heffner, T.G.5
Meltzer, L.T.6
Pugsley, T.A.7
-
8
-
-
56649105308
-
-
D.Q. Xu, Y.F. Wang, S.P. Luo, S. Zhang, A.G. Zhong, H. Chen, and Z.Y. Xu Adv. Synth. Catal. 350 2008 2610
-
(2008)
Adv. Synth. Catal.
, vol.350
, pp. 2610
-
-
Xu, D.Q.1
Wang, Y.F.2
Luo, S.P.3
Zhang, S.4
Zhong, A.G.5
Chen, H.6
Xu, Z.Y.7
-
10
-
-
73649139601
-
-
Y.F. Wang, W. Zhang, S.P. Luo, B.L. Li, A.B. Xia, A.G. Zhong, and D.Q. Xu Chem. Asian J. 4 2009 1834
-
(2009)
Chem. Asian J.
, vol.4
, pp. 1834
-
-
Wang, Y.F.1
Zhang, W.2
Luo, S.P.3
Li, B.L.4
Xia, A.B.5
Zhong, A.G.6
Xu, D.Q.7
-
13
-
-
69449106910
-
-
P.M. Habib, V. Kavala, B.R. Raju, C.W. Kuo, W.C. Huang, and C.F. Yao Eur. J. Org. Chem. 2009 4503
-
(2009)
Eur. J. Org. Chem.
, pp. 4503
-
-
Habib, P.M.1
Kavala, V.2
Raju, B.R.3
Kuo, C.W.4
Huang, W.C.5
Yao, C.F.6
-
15
-
-
48149097361
-
-
V.Y. Korotaev, V.Y. Sosnovskikh, I.B. Kutyashev, A.Y. Barkov, and Y.V. Shklyaev Tetrahedron Lett. 49 2008 5376
-
(2008)
Tetrahedron Lett.
, vol.49
, pp. 5376
-
-
Korotaev, V.Y.1
Sosnovskikh, V.Y.2
Kutyashev, I.B.3
Barkov, A.Y.4
Shklyaev, Y.V.5
-
22
-
-
67649396063
-
-
For the organocatalytic conjugate addition of malonates to nitroolefins, see: F.X. Chen, C. Shao, Q. Liu, P. Gong, C.L. Liu, and R. Wang Chirality 21 2009 600
-
(2009)
Chirality
, vol.21
, pp. 600
-
-
Chen, F.X.1
Shao, C.2
Liu, Q.3
Gong, P.4
Liu, C.L.5
Wang, R.6
-
23
-
-
58149402249
-
-
X.J. Li, K. Liu, H. Ma, J. Nie, and J.A. Ma Synlett 2008 3242
-
(2008)
Synlett
, pp. 3242
-
-
Li, X.J.1
Liu, K.2
Ma, H.3
Nie, J.4
Ma, J.A.5
-
27
-
-
35548945280
-
-
F.X. Chen, C. Shao, Q. Wang, P. Gong, D.Y. Zhang, B.Z. Zhang, and R. Wang Tetrahedron Lett. 48 2007 8456
-
(2007)
Tetrahedron Lett.
, vol.48
, pp. 8456
-
-
Chen, F.X.1
Shao, C.2
Wang, Q.3
Gong, P.4
Zhang, D.Y.5
Zhang, B.Z.6
Wang, R.7
-
31
-
-
11844302258
-
-
T. Okino, Y. Hoashi, T. Furukawa, X.N. 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.N.4
Takemoto, Y.5
-
34
-
-
77951095904
-
-
J.W. Xie, L.P. Fan, H. Su, X.S. Li, and D.C. Xu Org. Biomol. Chem. 8 2010 2117
-
(2010)
Org. Biomol. Chem.
, vol.8
, pp. 2117
-
-
Xie, J.W.1
Fan, L.P.2
Su, H.3
Li, X.S.4
Xu, D.C.5
-
36
-
-
77953688004
-
-
During the preparation of this manuscript, an asymmetric conjugate addition of malonates to 3-nitro-2H-chromenes was reported using chiral amine-nickel complexes as the catalysts, 10.1016/j.tetlet.2010.05.111
-
During the preparation of this manuscript, an asymmetric conjugate addition of malonates to 3-nitro-2H-chromenes was reported using chiral amine-nickel complexes as the catalysts, see: Chen, W. Y.; Ouyang, L.; Chen, R. Y.; Li, X. S. Tetrahedron Lett. doi: 10.1016/j.tetlet.2010.05.111.
-
Tetrahedron Lett.
-
-
Chen, W.Y.1
Ouyang, L.2
Chen, R.Y.3
Li, X.S.4
-
37
-
-
33750970292
-
-
A. Berkessel, S. Mukherjee, T.N. Müller, F. Cleemann, K. Roland, M. Brandenburg, J.M. Neudörfl, and J. Lex Org. Biomol. Chem. 4 2006 4319
-
(2006)
Org. Biomol. Chem.
, vol.4
, pp. 4319
-
-
Berkessel, A.1
Mukherjee, S.2
Müller, T.N.3
Cleemann, F.4
Roland, K.5
Brandenburg, M.6
Neudörfl, J.M.7
Lex, J.8
-
38
-
-
67649657963
-
-
X.J. Zhang, S.P. Liu, J.H. Lao, G.J. Du, M. Yan, and A.S.C. Chan Tetrahedron: Asymmetry 20 2009 1451
-
(2009)
Tetrahedron: Asymmetry
, vol.20
, pp. 1451
-
-
Zhang, X.J.1
Liu, S.P.2
Lao, J.H.3
Du, G.J.4
Yan, M.5
Chan, A.S.C.6
|