Henry reaction of fluorinated nitro compounds

Journal of Fluorine Chemistry

Volumn 133, Issue , 2012, Pages 108-114

  Hu, Huawei ^a   Huang, Yangen ^a   Guo, Yong ^b  

^a DONGHUA UNIVERSITY   (China)

^b SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

Author keywords

Aldehyde; Enantioselectivity; Fluorine; Henry reaction; Organocatalysis

Indexed keywords

EID: 84655161361     PISSN: 00221139     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jfluchem.2011.09.004     Document Type: Article

References (33)

1. N. Ono The Nitro Group in Organic Synthesis 2001 Wiley-VCH New York
2. J. Boruwa, N. Gogoi, P.P. Saikia, and N.C. Barua Tetrahedron: Asymmetry 17 2006 3315 3326
3. C. Palomo, M. Oiarbide, and A. Laso Eur. J. Org. Chem. 2007 2561 2574
4. Y. Sohtome, Y. Hashimoto, and K. Nagasawa Adv. Synth. Catal. 347 2005 1643 1648
5. C. Palomo, M. Oiarbide, and A. Mielgo Angew. Chem. Int. Ed. 43 2004 5442 5444
6. S. Gao, G. Xi, N. Li, C. Wang, and J. Ma Chin. J. Org. Chem. 30 2010 1811 1819
7. F.A. Luzzio Tetrahedron 57 2001 915 945
8. G. Rosini, and R. Ballini Synthesis 1988 833 847
9. G. Blay, V. Hernández-Olmos, and J.R. Pedro Chem. Commun. 2008 4840 8482
10. R.D. Chambers Fluorine in Organic Chemistry 2004 Blackwell Publishing Ltd./CRC Press Boca Raton, FL
11. T. Hiyama Organofluorine Compounds, Chemistry and Applications 2000 Springer-Verlag Berlin
12. P. Kirsch Modern Fluoroorganic Chemistry 2004 Wiley-VCH Weinheim
13. V.A. Soloshonok Fluorine-Containing Synthons, ACS Symposium Series 911 2005 Oxford University Press Washington, DC
14. K. Uneyama Organofluorine Chemistry 2006 Blackwell Publishing Oxford
15. K. Muller, C. Faeh, and F. Diederich Science 317 2007 1881 1886
16. M. Schlosser Angew. Chem. Int. Ed. 37 1998 1496 1513
17. D. O'Hagan Chem. Soc. Rev. 37 2008 308 319
18. S. Purser, P.R. Moore, S. Swallow, and V. Gouverneur Chem. Soc. Rev. 37 2008 320 330
19. K.L. Kirk Org. Process Res. Dev. 12 2008 305 321
20. D. O'Hagan J. Fluorine Chem. 131 2010 1071 1081
21. A.M. Thayer Chem. Eng. News 84 2006 15 24
22. J. Ma, and D. Cahard Chem. Rev. 104 2004 6119 6146
23. A.M.R. Smith, and K.K.M. Hii Chem. Rev. 111 2011 1637 1656
24. K. Shibatomi Synthesis 2010 2679 2702
25. M. Bella, and T. Gasperi Synthesis 2009 1583 1614
26. Y. Takeuchi, K. Nagata, and T. Koizumi J. Org. Chem. 52 1987 5061 5063
27. Y. Takeuchi, K. Nagata, and T. Koizumi J. Org. Chem. 54 1989 5453 5459
28. H. Cui, P. Li, X. Wang, Z. Chai, Y. Yang, Y. Cai, S. Zhu, and G. Zhao Tetrahedron 67 2011 312 317
29. R.A. Kunetsky, A.D. Dilman, M.I. Struchkova, P.A. Belyakov, V.A. Tartakovsky, and S.L. Ioffe Synthesis 2006 2265 2270
30. R. Ballini, L. Barboni, and G. Giarlo J. Org. Chem. 69 2004 6907 6908
31. N. Kornblum, H.O. Larson, R.K. Blackwood, D.D. Mooberry, E.P. Oliveto, and G.E. Graham J. Am. Chem. Soc. 78 1956 1497 1501
32. W. Peng, and J.M. Shreeve Tetrahedron Lett. 46 2005 4905 4909
33. P. Butler, B.T. Golding, G. Laval, H.L. Khouzani, R.R. Karimib, and M.M. Sadeghib Tetrahedron 63 2007 11160 11166