-
5
-
-
0035126119
-
-
For recent reviews of asymmetric Michael addition reactions, see:
-
For recent reviews of asymmetric Michael addition reactions, see:. Krause N., and Hoffmann-Röder A. Synthesis (2001) 171
-
(2001)
Synthesis
, pp. 171
-
-
Krause, N.1
Hoffmann-Röder, A.2
-
12
-
-
18844369828
-
-
For examples of organometallics catalyzed Michael addition of thiols, see:
-
For examples of organometallics catalyzed Michael addition of thiols, see:. Zielinska-Błajet M., Kowalczyk R., and Skarżewski J. Tetrahedron 61 (2005) 5235
-
(2005)
Tetrahedron
, vol.61
, pp. 5235
-
-
Zielinska-Błajet, M.1
Kowalczyk, R.2
Skarzewski, J.3
-
16
-
-
0000163641
-
-
Organocatalyzed Michael addition of thiols, see:
-
Organocatalyzed Michael addition of thiols, see:. Hiemstra H., and Wynberg H. J. Am. Chem. Soc. 103 (1981) 417
-
(1981)
J. Am. Chem. Soc.
, vol.103
, pp. 417
-
-
Hiemstra, H.1
Wynberg, H.2
-
21
-
-
0003463148
-
-
In contrast, the conversion of thioether to thiol (SH) requires harsh reaction conditions, see:, John Wiley and Sons, New York
-
In contrast, the conversion of thioether to thiol (SH) requires harsh reaction conditions, see:. Greene T.W., and Wuts P.G.M. Protective Groups in Organic Synthesis (1999), John Wiley and Sons, New York 454
-
(1999)
Protective Groups in Organic Synthesis
, pp. 454
-
-
Greene, T.W.1
Wuts, P.G.M.2
-
23
-
-
47749122232
-
-
For a book discussing organocatalysis, see:, Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim, Germany
-
For a book discussing organocatalysis, see:. Berkessel A., and Groger H. Asymmetric Organocatalysis-From Biomimetic Concepts to Applications in Asymmetric Synthesis (2005), Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim, Germany
-
(2005)
Asymmetric Organocatalysis-From Biomimetic Concepts to Applications in Asymmetric Synthesis
-
-
Berkessel, A.1
Groger, H.2
-
24
-
-
0035886887
-
-
For recent reviews of organocatalysis, see:
-
For recent reviews of organocatalysis, see:. Dalko P.I., and Moisan L. Angew. Chem., Int. Ed. 40 (2001) 3726
-
(2001)
Angew. Chem., Int. Ed.
, vol.40
, pp. 3726
-
-
Dalko, P.I.1
Moisan, L.2
-
26
-
-
4143094833
-
-
Special issue on organocatalysis: Acc. Chem. Res. 2004, 37, 487.
-
-
-
-
28
-
-
4143136647
-
-
Tian S.-K., Chen Y.-G., Hang J.-F., Tang L., McDaid P., and Deng L. 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
-
29
-
-
0006589268
-
-
For studies of the H-bonding interactions of ureas/thioureas with nitro, carbonyl, and imine groups, see:
-
For studies of the H-bonding interactions of ureas/thioureas with nitro, carbonyl, and imine groups, see:. Etter M.C. Acc. Chem. Res. 23 (1990) 120
-
(1990)
Acc. Chem. Res.
, vol.23
, pp. 120
-
-
Etter, M.C.1
-
35
-
-
11844302258
-
-
For Takemoto's amine thioureas catalysts, see: and references cited therein
-
For Takemoto's amine thioureas catalysts, see:. Okino T., Hoashi Y., Furukawa T., Xu X., and Takemoto Y. J. Am. Chem. Soc. 127 (2005) 119 and references cited therein
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 119
-
-
Okino, T.1
Hoashi, Y.2
Furukawa, T.3
Xu, X.4
Takemoto, Y.5
-
37
-
-
4344713238
-
-
For Jacobsen's urea and thiourea catalysts, see: and references cited therein
-
For Jacobsen's urea and thiourea catalysts, see:. Taylor M.S., and Jacobsen E.N. J. Am. Chem. Soc. 126 (2004) 10558 and references cited therein
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 10558
-
-
Taylor, M.S.1
Jacobsen, E.N.2
-
38
-
-
25444432564
-
-
We have developed binaphthyl derived amine thiourea for catalyzing: Morita-Baylis-Hillman reactions:
-
We have developed binaphthyl derived amine thiourea for catalyzing: Morita-Baylis-Hillman reactions:. Wang J., Li H., Duan W., Zu L., and Wang W. Org. Lett. 7 (2005) 4293
-
(2005)
Org. Lett.
, vol.7
, pp. 4293
-
-
Wang, J.1
Li, H.2
Duan, W.3
Zu, L.4
Wang, W.5
-
39
-
-
27144522622
-
-
Michael addition reaction:
-
Michael addition reaction:. Wang J., Li H., Yu X., Zu L., and Wang W. Org. Lett. 7 (2005) 4713
-
(2005)
Org. Lett.
, vol.7
, pp. 4713
-
-
Wang, J.1
Li, H.2
Yu, X.3
Zu, L.4
Wang, W.5
-
41
-
-
4143136647
-
-
For cinchona alkaloids-based derivatives catalysts, see:
-
For cinchona alkaloids-based derivatives catalysts, see:. Tian S.-K., Chen Y.-G., Hang J.-F., Tang L., McDaid P., and Deng L. 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
-
43
-
-
11244281650
-
-
Li H., Wang Y., Tang L., Wu F., Liu X., Guo C., Foxman B.M., and Deng L. 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
-
46
-
-
33646018493
-
-
note
-
See Supplementary data for X-ray crystallographic information; CCDC 283456 also contains Supplementary crystallographic data. These data can be obtained free of charge via www.ccdc.cam.ac.uk.
-
-
-
|