Baker's yeast-mediated enantioselective reduction of substituted fluorenones

Chemical Communications

Volumn , Issue 8, 2006, Pages 865-867

  Li, Feng ^a   Cui, Jingnan ^a   Qian, Xuhong ^b   Ren, Weimin ^a   Wang, Xingyong ^a  

^a DALIAN UNIVERSITY OF TECHNOLOGY   (China)

^b EAST CHINA UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

DIMETHYL SULFOXIDE; FLUORENONE DERIVATIVE; SOLVENT;

AGITATION; ARTICLE; ENANTIOSELECTIVITY; NONHUMAN; SACCHAROMYCES CEREVISIAE;

EID: 32844473766     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b516475c     Document Type: Article

References (27)

1. (a) R. A. Edwin, W. F. Robert, J. M. Grisar, C. K. James, L. W. David and D. M. Gerald, J. Med. Chem., 1974, 17, 882;
2. (b) R. A. Edward and E. G. Felix, J. Med Chem., 1974, 17, 1009;
3. (c) M. Schmittel, M. Strittmatter, W. A. Schenk and M. Z. Hagel, Z. Naturforsch., B: Chem. Sci., 1998, 53, 1015;
4. (d) D. Rodriguez, A. Navarro, L. Castedo, D. Dominguez and C. Saa, Org. Lett., 2000, 2, 1497;
5. (e) A. Torrens, J. Mas, A. Port, J. A. Castrillo, O. Sanfeliu, X. Guitart, A. Dordal, G. Romero, M. A. Fisas, E. Sanchez, E. Hemandez, P. Perez, R. Perez and H. Buschmann, J. Med. Chem., 2005, 48, 2080.
6. (a) D. J. Abraham, P. E. Kennedy, A. S. Mehanna, D. C. Patwa and F. L. Williams, J. Med. Chem., 1984, 27, 967;
7. (b) R. Bebernitz, G. Argentieri, B. Battle, C. Brennan, B. Balkan, B. F. Burkey, M. Eckhardt, J. Gao, P. Kapa, R. J. Strohschein, H. F. Schuster, M. Wilson and D. D. Xu, J. Med. Chem, 2001, 44, 2601;
8. (c) P. C. Ting, J. F. Lee, M. M. Albanese, W. C. Tom, D. M. Solomon, A. Robert, Y. S. Neng and W. Robert, Bioorg. Med Chem. Lett., 2002, 12, 2643;
9. (d) S. Ulmschneider, U. M. Vieira, C. D. Klein, I. Antes, T. Lengauer and R. W. Hartmann, J. Med Chem., 2005, 48, 1563.
10. M. Dahrouch, B. Valentin, M. R. Baudet and A. Castel, Inorg. Chim. Acta, 1998, 277, 98.
11. (a) P. Wan and E. Krogh, J. Chem. Soc., Chem. Commun., 1985, 1207;
12. (b) E. Gaillard, M. A. Fox and P. Wan, J. Am. Chem. Soc., 1989, 111, 2180;
13. (c) P. Wan and E. Krogh, J. Am. Chem. Soc., 1989, 111, 4887;
14. (d) R. A. McClelland, N. Mathivanan and S. Steenken, J. Am. Chem. Soc., 1990, 112, 4857;
15. (e) G. G. Gurzadyan and S. Steenken, Chem.-Eur. J., 2001, 7, 1808.
16. (a) J. A. McCubbin, X. Tong, R. Wang, Y. Zhao, V. Snieckus and R. P. Lemieux, J. Am. Chem. Soc., 2004, 126, 1161;
17. (b) J. A. McCubbin, X. Tong, Y. Zhao, V. Snieckus and R. P. Lemieux, Chem. Mater., 2005, 17, 2574.
18. (a) Z. Yu, F. L. Calahorra and D. Velasco, Tetrahedron: Asymmetry, 2000, 11, 3221;
19. (b) Z. Yu, F. L. Calahorra and D. Velasco, Tetrahedron: Asymmetry, 2000, 11, 3227.
20. (a) S. Servi, Synthesis, 1990, 1;
21. (b) R. Csuk and B. I. Glanzer, Chem. Rev., 1991, 91, 49;
22. (c) E. G. Urdiales, I. Alfonso and V. Gotor, Chem. Rev., 2005, 105, 313.
23. (a) M. Chartrain, J. Lynch, W. B. Choi, H. Churchill, S. Patel, S. Yamazaki, R. Volante and R. Greasham, J. Mol. Catal. B: Enzym., 2000, 8, 285;
24. (b) R. Sébastien, A. Vanessa, N. Michel and T. L. Laurence, Adv. Synth. Catal., 2001, 343, 738.
25. (a) F. Li, J. Cui, X. Qian and R. Zhang, Chem. Commun., 2004, 2338;
26. (b) F. Li, J. Cui, X. Qian, R. Zhang and Y. Xiao, Chem. Commun., 2005, 1901.
27. A. C. Darby, M. K. Hargreaves and D. A. Raval, J. Chem. Soc. D, 1970, 1554.