-
1
-
-
9644306326
-
-
Jacobsen E.N., Pfaltz A., and Yamamoto H. (Eds), Spinger, Berlin
-
In: Jacobsen E.N., Pfaltz A., and Yamamoto H. (Eds). Comprehensive Asymmetric Synthesis I-III (1999), Spinger, Berlin
-
(1999)
Comprehensive Asymmetric Synthesis I-III
-
-
-
5
-
-
0037454989
-
-
Shinohara T., Arai M.A., Wakita K., Arai T., and Sasai H. Tetrahedron Lett. 44 (2003) 711-714
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 711-714
-
-
Shinohara, T.1
Arai, M.A.2
Wakita, K.3
Arai, T.4
Sasai, H.5
-
6
-
-
0038345989
-
-
Muthiah C., Arai M.A., Shinohara T., Arai T., Takizawa S., and Sasai H. Tetrahedron Lett. 44 (2003) 5201-5204
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 5201-5204
-
-
Muthiah, C.1
Arai, M.A.2
Shinohara, T.3
Arai, T.4
Takizawa, S.5
Sasai, H.6
-
8
-
-
0030831034
-
-
Chan A.S.C., Hu W., Pai C.-C., Lau C.-P., Jiang Y., Mi A., Yan M., Sun J., Lou R., and Deng J. J. Am. Chem. Soc. 119 (1997) 9570-9571
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 9570-9571
-
-
Chan, A.S.C.1
Hu, W.2
Pai, C.-C.3
Lau, C.-P.4
Jiang, Y.5
Mi, A.6
Yan, M.7
Sun, J.8
Lou, R.9
Deng, J.10
-
9
-
-
0032544766
-
-
Jiang Y., Xue S., Li Z., Deng J., Mi A., and Chan A.S.C. Tetrahedron: Asymmetry 9 (1998) 3185-3189
-
(1998)
Tetrahedron: Asymmetry
, vol.9
, pp. 3185-3189
-
-
Jiang, Y.1
Xue, S.2
Li, Z.3
Deng, J.4
Mi, A.5
Chan, A.S.C.6
-
10
-
-
0037034833
-
-
Fu Y., Xie J.-H., Hu A.-G., Zhou H., Wang L.-X., and Zhou Q.-L. Chem. Commun. (2002) 480-481
-
(2002)
Chem. Commun.
, pp. 480-481
-
-
Fu, Y.1
Xie, J.-H.2
Hu, A.-G.3
Zhou, H.4
Wang, L.-X.5
Zhou, Q.-L.6
-
11
-
-
0037007906
-
-
Hu A.-G., Fu Y., Xie J.-H., Zhou H., Wang L.-X., and Zhou Q.-L. Angew. Chem., Int. Ed. 41 (2002) 2348-2350
-
(2002)
Angew. Chem., Int. Ed.
, vol.41
, pp. 2348-2350
-
-
Hu, A.-G.1
Fu, Y.2
Xie, J.-H.3
Zhou, H.4
Wang, L.-X.5
Zhou, Q.-L.6
-
12
-
-
0037458797
-
-
Zhou H., Wang W.-H., Fu Y., Xie J.-H., Shi W.-J., Wang L.-X., and Zhou Q.-L. J. Org. Chem. 68 (2003) 1582-1584
-
(2003)
J. Org. Chem.
, vol.68
, pp. 1582-1584
-
-
Zhou, H.1
Wang, W.-H.2
Fu, Y.3
Xie, J.-H.4
Shi, W.-J.5
Wang, L.-X.6
Zhou, Q.-L.7
-
13
-
-
0037448876
-
-
Xie J.-H., Wang L.-X., Fu Y., Zhu S.-F., Fan B.-M., Duan H.-F., and Zhou Q.-L. J. Am. Chem. Soc. 125 (2003) 4404-4405
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 4404-4405
-
-
Xie, J.-H.1
Wang, L.-X.2
Fu, Y.3
Zhu, S.-F.4
Fan, B.-M.5
Duan, H.-F.6
Zhou, Q.-L.7
-
19
-
-
0347090265
-
-
Wakita K., Arai M.A., Kato T., Shinohara T., and Sasai H. Heterocycles 62 (2004) 831-838
-
(2004)
Heterocycles
, vol.62
, pp. 831-838
-
-
Wakita, K.1
Arai, M.A.2
Kato, T.3
Shinohara, T.4
Sasai, H.5
-
21
-
-
0142090884
-
-
Takizawa S., Honda Y., Arai M.A., Kato T., and Sasai H. Heterocycles 60 (2003) 2551-2556
-
(2003)
Heterocycles
, vol.60
, pp. 2551-2556
-
-
Takizawa, S.1
Honda, Y.2
Arai, M.A.3
Kato, T.4
Sasai, H.5
-
24
-
-
0142131972
-
-
Jacobsen E.N., Pfaltz A., and Yamamoto H. (Eds), Wiley, New York
-
Mikami K., and Terada M. In: Jacobsen E.N., Pfaltz A., and Yamamoto H. (Eds). Comprehensive Asymmetric Catalysis Vol. 3, Chapter 32 (2000), Wiley, New York 1140-1174
-
(2000)
Comprehensive Asymmetric Catalysis
, vol.3 Chapter 32
, pp. 1140-1174
-
-
Mikami, K.1
Terada, M.2
-
29
-
-
0032491582
-
-
Also see:
-
Also see:. Chavarot M., Byrne J.J., Chavant P.Y., Pardillos-Guindet J., and Vallee Y. Tetrahedron: Asymmetry 9 (1998) 3889-3894
-
(1998)
Tetrahedron: Asymmetry
, vol.9
, pp. 3889-3894
-
-
Chavarot, M.1
Byrne, J.J.2
Chavant, P.Y.3
Pardillos-Guindet, J.4
Vallee, Y.5
-
33
-
-
0346874405
-
-
We have also reported polymer supported multicomponent catalysts for carbonyl-ene reactions, see:
-
We have also reported polymer supported multicomponent catalysts for carbonyl-ene reactions, see:. Takizawa S., Somei H., Jayaprakash D., and Sasai H. Angew. Chem., Int. Ed. 42 (2003) 5711-5714
-
(2003)
Angew. Chem., Int. Ed.
, vol.42
, pp. 5711-5714
-
-
Takizawa, S.1
Somei, H.2
Jayaprakash, D.3
Sasai, H.4
-
34
-
-
0141520400
-
-
Sekiguti T., Iizuka Y., Takizawa S., Jayaprakash D., Arai T., and Sasai H. Org. Lett. 5 (2003) 2647-2650
-
(2003)
Org. Lett.
, vol.5
, pp. 2647-2650
-
-
Sekiguti, T.1
Iizuka, Y.2
Takizawa, S.3
Jayaprakash, D.4
Arai, T.5
Sasai, H.6
-
37
-
-
0032540647
-
-
Evans D.A., Burgey C.S., Paras N.A., Vojkovsky T., and Tregay S.W. J. Am. Chem. Soc. 120 (1998) 5824-5825
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 5824-5825
-
-
Evans, D.A.1
Burgey, C.S.2
Paras, N.A.3
Vojkovsky, T.4
Tregay, S.W.5
-
39
-
-
0034706033
-
-
Evans D.A., Tregay S.W., Burgey C.S., Paras N.A., and Vojkovsky T. J. Am. Chem. Soc. 122 (2000) 7936-7943
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 7936-7943
-
-
Evans, D.A.1
Tregay, S.W.2
Burgey, C.S.3
Paras, N.A.4
Vojkovsky, T.5
-
46
-
-
4544385176
-
-
Caplan N.A., Hancock F.E., Page P.C.B., and Hutchings G.J. Angew. Chem., Int. Ed. 43 (2004) 1685-1688
-
(2004)
Angew. Chem., Int. Ed.
, vol.43
, pp. 1685-1688
-
-
Caplan, N.A.1
Hancock, F.E.2
Page, P.C.B.3
Hutchings, G.J.4
-
52
-
-
0036371962
-
-
and references cited therein
-
Trost B.M. Chem. Pharm. Bull. 50 (2002) 1-14 and references cited therein
-
(2002)
Chem. Pharm. Bull.
, vol.50
, pp. 1-14
-
-
Trost, B.M.1
-
53
-
-
33847628789
-
-
note
-
2: C, 71.66; H, 9.50, N, 8.80. Found: C, 71.69; H, 9.51; N, 8.64.
-
-
-
-
54
-
-
33847629616
-
-
note
-
2: C, 72.58; H, 8.33, N, 8.91. Found: C, 72.51; H, 8.44; N, 9.02.
-
-
-
-
55
-
-
33847679631
-
-
note
-
2) and significant low field shifts of the methyne protons, which indicated an efficient complexation due to the structural geometry, while (M)-4 gave only insoluble material.
-
-
-
-
56
-
-
33847654693
-
-
note
-
2 (1:1) at rt for 24 h.
-
-
-
-
57
-
-
33847657497
-
-
note
-
The Pd-catalyzed asymmetric tandem cyclization of alkenyl alcohol 17 using newly synthesized ligand 3 gave unsatisfactory results. See Refs. 2b, 4a and 11h.{A figure is presented}
-
-
-
-
58
-
-
33847684731
-
-
note
-
The absolute configuration of the major enantiomer of 7a was determined to be S by comparing the HPLC profile with the values reported in Ref. 7d.
-
-
-
-
59
-
-
33847607888
-
-
note
-
4 and concentrated. The residue was purified by silica gel column chromatography (hexane/ethyl acetate = 5/1) to give product 7. The enantiomeric excess of the products was determined by HPLC analysis using chiral stationary phase column (Daicel Chiralpak AS, hexane/i-PrOH = 10/1, flow rate = 0.5 mL/min).
-
-
-
|