-
4
-
-
4143094833
-
-
Special issue on organocatalysis: Acc. Chem. Res. 37 2004 487
-
(2004)
Acc. Chem. Res.
, vol.37
, pp. 487
-
-
-
6
-
-
4143136647
-
-
S.-K. Tian, Y.-G. Chen, J.-F. Hang, L. Tang, P. McDaid, and L. Deng Acc. Chem. Res. 37 2004 621
-
(2004)
Acc. Chem. Res.
, vol.37
, pp. 621
-
-
Tian, S.-K.1
Chen, Y.-G.2
Hang, J.-F.3
Tang, L.4
McDaid, P.5
Deng, L.6
-
7
-
-
14844316261
-
-
Aldehydes as Michael donors, see: W. Wang, J. Wang, and H. Li Angew. Chem., Int. Ed. 43 2005 1369
-
(2005)
Angew. Chem., Int. Ed.
, vol.43
, pp. 1369
-
-
Wang, W.1
Wang, J.2
Li, H.3
-
11
-
-
22144459070
-
-
Y. Hayashi, H. Gotoh, T. Hayashi, and M. Shoji Angew. Chem., Int. Ed. 44 2005 4212
-
(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 4212
-
-
Hayashi, Y.1
Gotoh, H.2
Hayashi, T.3
Shoji, M.4
-
16
-
-
3543065878
-
-
Ketones as Michael donors, see: T. Ishii, S. Fiujioka, Y. Sekiguchi, and H. Kotsuki J. Am. Chem. Soc. 126 2004 9558
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 9558
-
-
Ishii, T.1
Fiujioka, S.2
Sekiguchi, Y.3
Kotsuki, H.4
-
22
-
-
27144522622
-
-
For 1,3-dicarbonyl and related stabilized carbanions as Michael donors, see: J. Wang, H. Li, W.-H. Duan, L.-S. Zu, and W. Wang Org. Lett. 7 2005 4713
-
(2005)
Org. Lett.
, vol.7
, pp. 4713
-
-
Wang, J.1
Li, H.2
Duan, W.-H.3
Zu, L.-S.4
Wang, W.5
-
23
-
-
11244281650
-
-
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
-
28
-
-
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
-
53
-
-
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
-
54
-
-
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
-
55
-
-
0006589268
-
-
For studies of the H-bonding interactions of ureas/thioureas with nitro, carbonyl and imine groups, see: M.C. Etter Acc. Chem. Res. 23 1990 120
-
(1990)
Acc. Chem. Res.
, vol.23
, pp. 120
-
-
Etter, M.C.1
-
61
-
-
0003554758
-
-
In addition to amine thiourea VI, other thiourea-based organocatalysts have been reported. For Jacobsen's urea and thiourea catalysis, see: M.S. Sigman, and E.N. Jacobsen J. Am. Chem. Soc. 120 1998 4901
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 4901
-
-
Sigman, M.S.1
Jacobsen, E.N.2
-
67
-
-
19544393388
-
-
For cinchona alkaloid-based thioureas, see: B. Vakulya, S. Varga, A. Csampai, and T. Soos Org. Lett. 7 2005 1967
-
(2005)
Org. Lett.
, vol.7
, pp. 1967
-
-
Vakulya, B.1
Varga, S.2
Csampai, A.3
Soos, T.4
-
69
-
-
25444432564
-
-
Recently, we have developed binaphthyl-based amine thioureas for asymmetric organocatalysis, see: J. Wang, H. Li, X.-H. Yu, and W. Wang Org. Lett. 7 2005 4293 and Ref. 5a
-
(2005)
Org. Lett.
, vol.7
, pp. 4293
-
-
Wang, J.1
Li, H.2
Yu, X.-H.3
Wang, W.4
-
70
-
-
33644906810
-
-
See Supplementary data for X-ray crystallographic information; CCDC 283455 also contains the supplementary crystallographic data. These data can be obtained free of charge via www.ccdc.cam.ac.uk.
-
-
-
|