One-pot synthesis of spirooxindole derivatives catalyzed by lipase in the presence of water

Advanced Synthesis and Catalysis

Volumn 353, Issue 2-3, 2011, Pages 371-375

  Chai, She Jie ^a   Lai, Yi Feng ^a   Xu, Jiang Cheng ^a   Zheng, Hui ^a   Zhu, Qing ^b   Zhang, Peng Fei ^a  

^a HANGZHOU NORMAL UNIVERSITY   (China)

^b ZHEJIANG UNIVERSITY OF TECHNOLOGY   (China)

Author keywords

enzymatic reactions; lipase catalysis; multistep conversions; one pot synthesis; spirooxindole derivatives

Indexed keywords

EID: 79951831704     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.201000523     Document Type: Article

References (34)

1. C. C. Galliford, K. A. Scheidt, Angew. Chem. 2007, 119, 8902-8912
2. Angew. Chem. Int. Ed. 2007, 46, 8748-8758
3. K. Ding, Y. P. Lu, N. Coleska, J. Med. Chem. 2006, 49, 3432-3435.
4. J. P. Nandy, M. Prakesch, S. Khadem, P. T. Reddy, U. Sharma, P. Arya, Chem. Rev. 2009, 109, 1999-2060
5. M. Pettersson, D. Knueppel, S. F. Martin., Org. Lett. 2007, 9, 4623-4626
6. S. Shangary, etaal., Proc. Natl. Acad. Sci. U.S. 2008, 105, 3933-3938.
7. C. Marti, E. M. Carreira, Eur. J. Org. Chem. 2003, 2209-2219.
8. C. V. Galliford, J. A. Martenson, C. Stern, K. A. Scheidt, Chem. Commun. 2007, 631-633.
9. D. Hojo, K. Noguchi, M. Hirano, K. Tanaka, Angew. Chem. 2008, 120, 5904-5906
10. Angew. Chem. Int. Ed. 2008, 47, 5820-5822
11. R. Shintani, S. Y. Hayashi, M. Murakami, M. Takeda, T. Hayashi, Org. Lett. 2009, 11, 3754-3756.
12. C. Meyers, E. M. Carreira, Angew. Chem. 2003, 115, 718-720
13. C. Marti, E. M. Carreira, J. Am. Chem. Soc. 2005, 127, 11505-11515
14. G. Wuitschik, M. Rogers-Evans, A. Buckl, M. Bernasconi, M. Marki, T. Godel, H. Fischer, B. Wagner, I. Parrilla, F. Schuler, J. Schneider, A. Alker, W. B. Schweizer, K. Muller, E. M. Carreira, Angew. Chem. 2008, 120, 4588-4591
15. Angew. Chem. Int. Ed. 2008, 47, 4512-4515.
16. P. R. Sebahar, R. M. Williams, J. Am. Chem. Soc. 2000, 122, 5666-5667
17. T. Onishi, P. R. Sebahar, R. M. Williams, Org. Lett. 2003, 5, 3135-3137.
18. X. H. Chen, Q. Wei, S. W. Luo, H. Xiao, L. Z. Gong, J. Am. Chem. Soc. 2009, 131, 13819-13825.
19. S. J. Chai, Y. F. Lai, H. Zheng, P. F. Zhang, Helv. Chim. Acta 2010, 93, 2231-2236
20. Y. F. Lai, H. Zheng, S. J. Chai, P. F. Zhang, X. Z. Chen, Green Chem. 2010, 12, 1917-1918.
21. C. Branneby, P. Carlqvist, A. Magnusson, K. Hult, T. Brinck, P. Berglund, J. Am. Chem. Soc. 2003, 125, 874-875
22. C. Li, X. W. Feng, N. Wang, Y. J. Zhou, X. Q. Yu, Green Chem. 2008, 10, 616-618.
23. M. Svedendahl, K. Hult, P. Berglund, J. Am. Chem. Soc. 2005, 127, 17988-17989
24. F. W. Lou, B. K. Liu, Q. Wu, D. S. Lu, X. F. Lin, Adv. Synth. Catal. 2008, 350, 1959-1962
25. O. Torre, I. Alfonso, V. Gotor, Chem. Commun. 2004, 1724-1725.
26. S. Akai, K. Tanimoto, Y. Kita, Angew. Chem. 2004, 116, 1431-1434
27. Angew. Chem. Int. Ed. 2004, 43, 1407-1410.
28. X. W. Feng, C. Li, N. Wang, K. Li, W. W. Zhang, Z. Wang. X. Q. Yu, Green Chem. 2009, 11, 1933-1936.
29. K. Li, T. He, C. Li, X. W. Feng, N. Wang, X. Q. Yu, Green Chem. 2009, 11, 777-779.
30. S. Akai, K. Tanimoto, Y. Kita, Angew. Chem. 2004, 116, 1431-1434
31. Angew. Chem. Int. Ed. 2004, 43, 1407-1410
32. S. Akai, T. Naka, S. Omura, K. Tanimoto, M. Imanishi, Y. Takebe, M. Matsugi, Y. Kita, Chem. Eur. J. 2002, 8, 4255-4264.
33. J. Duwensee, S. Wenda, W. Ruth, U. Kragl, Org. Process Res. Dev. 2010, 14, 48-57
34. P. Lozano, R. Piamtongkam, K. Kohns, T. D. Diego, M. Vaultier, J. L. Iborra, Green Chem. 2007, 9, 780-784.