-
6
-
-
37049113731
-
-
Grigg R., Malone J.F., Mitchell T.R.B., Ramasubbu A., and Scott R.M. J. Chem. Soc., Perkin Trans. 1 (1984) 1745
-
(1984)
J. Chem. Soc., Perkin Trans. 1
, pp. 1745
-
-
Grigg, R.1
Malone, J.F.2
Mitchell, T.R.B.3
Ramasubbu, A.4
Scott, R.M.5
-
10
-
-
0742288606
-
-
Özdemir I., Çetinkaya E., Çetinkaya B., Çiçek M., Sémeril D., Bruneau C., and Dixneuf P.H. Eur. J. Inorg. Chem. (2004) 418
-
(2004)
Eur. J. Inorg. Chem.
, pp. 418
-
-
Özdemir, I.1
Çetinkaya, E.2
Çetinkaya, B.3
Çiçek, M.4
Sémeril, D.5
Bruneau, C.6
Dixneuf, P.H.7
-
17
-
-
33845193996
-
-
Bray K.L., Lloyd-Jones G.C., Paz-Muñoz M., Slatford P.A., Tan E.H.P., Tyler-Mahon A.R., and Worthington P.A. Chem.-Eur. J. 12 (2006) 8650
-
(2006)
Chem.-Eur. J.
, vol.12
, pp. 8650
-
-
Bray, K.L.1
Lloyd-Jones, G.C.2
Paz-Muñoz, M.3
Slatford, P.A.4
Tan, E.H.P.5
Tyler-Mahon, A.R.6
Worthington, P.A.7
-
18
-
-
34547464719
-
-
Song Y.-J., Jung I.G., Lee H., Lee Y.T., Chung Y.K., and Jang H.-Y. Tetrahedron Lett. 48 (2007) 6142
-
(2007)
Tetrahedron Lett.
, vol.48
, pp. 6142
-
-
Song, Y.-J.1
Jung, I.G.2
Lee, H.3
Lee, Y.T.4
Chung, Y.K.5
Jang, H.-Y.6
-
19
-
-
33845256438
-
-
Fairlamb I.J.S., Grant S., Tommasi S., Lynam J.M., Bondini M., Dong H., Lin Z., and Whitwood A.C. Adv. Synth. Catal. 348 (2006) 2515
-
(2006)
Adv. Synth. Catal.
, vol.348
, pp. 2515
-
-
Fairlamb, I.J.S.1
Grant, S.2
Tommasi, S.3
Lynam, J.M.4
Bondini, M.5
Dong, H.6
Lin, Z.7
Whitwood, A.C.8
-
28
-
-
0004145285
-
-
Wasserscheid P., and Welton T. (Eds), Wiley-VCH, Weinheim
-
In: Wasserscheid P., and Welton T. (Eds). Ionic Liquids in Synthesis. 2nd ed. (2007), Wiley-VCH, Weinheim
-
(2007)
Ionic Liquids in Synthesis. 2nd ed.
-
-
-
36
-
-
0036430377
-
-
Csihony S.z., Fischmeister C., Bruneau C., Horváth I.T., and Dixneuf P.H. New J. Chem. 26 (2002) 1667
-
(2002)
New J. Chem.
, vol.26
, pp. 1667
-
-
Csihony, S.z.1
Fischmeister, C.2
Bruneau, C.3
Horváth, I.T.4
Dixneuf, P.H.5
-
37
-
-
33947603439
-
-
Thurier C., Fischmeister C., Bruneau C., Olivier-Bourbigou H., and Dixneuf P.H. J. Mol. Catal. A: Chem. 268 (2007) 127
-
(2007)
J. Mol. Catal. A: Chem.
, vol.268
, pp. 127
-
-
Thurier, C.1
Fischmeister, C.2
Bruneau, C.3
Olivier-Bourbigou, H.4
Dixneuf, P.H.5
-
38
-
-
21744449302
-
-
Hubert C., Renaud J.-L., Fischmeister C., Demerseman B., and Bruneau C. J. Mol. Catal. A: Chem. 237 (2005) 161
-
(2005)
J. Mol. Catal. A: Chem.
, vol.237
, pp. 161
-
-
Hubert, C.1
Renaud, J.-L.2
Fischmeister, C.3
Demerseman, B.4
Bruneau, C.5
-
40
-
-
40849106899
-
-
note
-
2].
-
-
-
-
42
-
-
34548251832
-
-
Pernak J., Feder-Kubis J., Cieniecka-Rosłonkievicz A., Fischmeister C., Griffin S.T., and Rogers R.D. New J. Chem. 31 (2007) 879
-
(2007)
New J. Chem.
, vol.31
, pp. 879
-
-
Pernak, J.1
Feder-Kubis, J.2
Cieniecka-Rosłonkievicz, A.3
Fischmeister, C.4
Griffin, S.T.5
Rogers, R.D.6
-
44
-
-
35048815465
-
-
Kumar V., Olsen C.E., Schäffer S.J.C., Parmar V.S., and Malhorta S.V. Org. Lett. 9 (2007) 3905
-
(2007)
Org. Lett.
, vol.9
, pp. 3905
-
-
Kumar, V.1
Olsen, C.E.2
Schäffer, S.J.C.3
Parmar, V.S.4
Malhorta, S.V.5
-
45
-
-
28844495851
-
-
Baudequin C., Brégeon D., Levillain J., Guillen F., Plaquevent J.-C., and Gaumont A.-C. Tetrahedron : Asymmetry 16 (2005) 3921
-
(2005)
Tetrahedron : Asymmetry
, vol.16
, pp. 3921
-
-
Baudequin, C.1
Brégeon, D.2
Levillain, J.3
Guillen, F.4
Plaquevent, J.-C.5
Gaumont, A.-C.6
-
47
-
-
33746298422
-
-
Gausepohl R., Buskens P., Kleinen J., Bruckmann A., Lehmann C.W., Klankermayer J., and Leitner W. Angew. Chem., Int. Ed. 45 (2006) 3689
-
(2006)
Angew. Chem., Int. Ed.
, vol.45
, pp. 3689
-
-
Gausepohl, R.1
Buskens, P.2
Kleinen, J.3
Bruckmann, A.4
Lehmann, C.W.5
Klankermayer, J.6
Leitner, W.7
-
48
-
-
34250889278
-
-
Schulz P.S., Müller N., Bösmann A., and Wasserscheid P. Angew. Chem., Int. Ed. 46 (2007) 1293
-
(2007)
Angew. Chem., Int. Ed.
, vol.46
, pp. 1293
-
-
Schulz, P.S.1
Müller, N.2
Bösmann, A.3
Wasserscheid, P.4
-
52
-
-
13444256295
-
-
Ding J., Desikan V., Han X.-X., Xiao T.L., Ding R., Jenks W.S., and Armstrong D.W. Org. Lett. 7 (2005) 335
-
(2005)
Org. Lett.
, vol.7
, pp. 335
-
-
Ding, J.1
Desikan, V.2
Han, X.-X.3
Xiao, T.L.4
Ding, R.5
Jenks, W.S.6
Armstrong, D.W.7
-
53
-
-
40849141258
-
-
note
-
At 20 °C, 1a was isolated in 89% yield. At 0 °C, 80% conversion was reached but isomerised starting material was detected as the major product.
-
-
-
-
55
-
-
42149132278
-
-
Crooks G.R., Jonhson B.F.G., Lewis J., Williams I.G., and Galem G. J. Chem. Soc. A (1969) 2761
-
(1969)
J. Chem. Soc. A
, pp. 2761
-
-
Crooks, G.R.1
Jonhson, B.F.G.2
Lewis, J.3
Williams, I.G.4
Galem, G.5
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