Chiral biphosphine ligands for the Ru-catalyzed enantioselective hydrogenation of β-ketoesters

Tetrahedron Asymmetry

Volumn 15, Issue 14, 2004, Pages 2185-2188

  Sun, Yanhui ^a   Wan, Xiaobing ^b   Guo, Minjie ^b   Wang, Donghui ^b   Dong, Xicheng ^b   Pan, Yi ^a   Zhang, Zhaoguo ^b  

^a NANJING UNIVERSITY   (China)

^b SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

PHOSPHINE DERIVATIVE; RUTHENIUM;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CHIRALITY; ENANTIOSELECTIVITY; HYDROGENATION; PRIORITY JOURNAL;

EID: 3843133240     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetasy.2004.04.034     Document Type: Article

References (31)

1. Noyori R. Asymmetric Catalysis in Organic Synthesis. 1994;Wiley, New York
2. Ojima I. Catalytic Asymmetric Synthesis. 2nd ed.:2000;Wiley, New York
3. Brown J.M. Jacobsen E.N, Pfaltz A., Yamamoto H. Comprehensive Asymmetric Catalysis. 1999;Springer, Berlin
4. Knowles W.S., Sabacky M.J. J. Chem. Soc., Chem. Commun. 1968;1445
5. Horner L., Siegel H., Büthe H. Angew. Chem., Int. Ed. Engl. 7:1968;942
6. Kagan H.B., Dang T.-P. J. Am. Chem. Soc. 94:1972;6429
7. Miyashita A., Yasuda H., Takaya H., Toriumi K., Ito T., Souchi T., Noyori R. J. Am. Chem. Soc. 102:1980;7932
8. Noyori R., Takaya H. Acc. Chem. Res. 23:1990;345
9. Noyori R. Chem. Soc. Rev. 18:1989;187
10. Schmid R., Cereghetti M., Heiser B., Schönholzer P., Hansen H.-J. Helv. Chim. Acta. 71:1988;897
11. Schmid R., Foricher J., Cereghetti M., Schönholzer P. Helv. Chim. Acta. 74:1991;370
12. Schmid R., Broger E.A., Cereghetti M., Crameri Y., Foricher J., Lalonde M., Müller R.K., Scalone M., Schoettel G., Zutter U. Pure Appl. Chem. 68:1996;131
13. Zhang Z., Qian H., Longmire J., Zhang X. J. Org. Chem. 65:2000;6223
14. Pai C.-C., Lin C.-W., Lin C.-C., Chen C.-C., Chan A.S.C. J. Am. Chem. Soc. 122:2000;11513
15. Wu J., Chen H., Kwok W.-H., Guo R., Zhou Z.-Y., Yeung C.-H., Chan A.S.C. J. Org. Chem. 67:2002;7908
16. Wu J., Chen H., Kwok W.-H., Lam K.-H., Zhou Z.-Y., Yeung C.-H., Chan A.S.C. Tetrahedron Lett. 43:2002;1539
17. Saito T., Yokozawa T., Ishizaki T., Moroi T., Sayo N., Miura T., Kumobayashi H. Adv. Synth. Catal. 343:2001;264
18. Jeulin S., Duprat de Paule S., Ratovelomanana-Vidal V., Genêt J.-P., Champion N., Dellis P. Angew. Chem., Int. Ed. 43:2004;320
19. Pai C.-C., Li Y.-M., Zhou Z.-Y., Chan A.S.C. Tetrahedron Lett. 43:2002;2789
20. Qiu L., Qi J., Pai C.-C., Chan S., Zhou Z.-Y., Choi M.C.K., Chan A.S.C. Org. Lett. 4:2002;4599
21. Duprat de Paule S., Jeulin S., Ratovelomanana-Vidal V., Genêt J.-P., Champion N., Dellis P. Tetrahedron Lett. 44:2003;823
22. Genêt J.-P. Acc. Chem. Res. 36:2003;908
23. Casey C.P., Whiteker G.T. Isr. J. Chem. 30:1990;299
24. Casey C.P., Whiteker G.T. J. Org. Chem. 55:1990;1394
25. Casey C.P., Whiteker G.T., Melville M.G., Petrovich L.M., Gavney J.A., Powell D.R. J. Am. Chem. Soc. 114:1992;5535
26. Tani K., Brown L.D., Ahmed J., Ibers J.A., Yokota M., Nakamura A., Otsuka S. J. Am. Chem. Soc. 99:1977;7876
27. Roberts N.K., Wild S.B. J. Am. Chem. Soc. 101:1979;6254
28. Roberts N.K., Wild S.B. J. Chem. Soc., Dalton Trans. 1979;2015
29. Kyba E.P., Rines S.P. J. Org. Chem. 47:1982;4800
30. Mashima K., Kusano K.-H., Sato N., Matsumura Y.-I., Nozaki K., Kumobayashi H., Sayo N., Hori Y., Ishizaki T., Akutagawa S., Takaya H. J. Org. Chem. 59:1994;3064
31. Kitamura M., Ohkuma T., Takaya H., Noyori R. Tetrahedron Lett. 29:1988;1555