Solid sodium stannate as a high-efficiency superbase catalyst for anti-Markovnikov hydroamination and hydroalkoxylation of electron-deficient olefins under mild conditions

Catalysis Communications

Volumn 12, Issue 8, 2011, Pages 712-716

  Zhang, Shuguo ^a   Wei, Yudan ^a   Yin, Shuangfeng ^a   Au, Chak Tong ^a,b  

^a HUNAN UNIVERSITY   (China)

^b HONG KONG BAPTIST UNIVERSITY   (Hong Kong)

Author keywords

Acrylonitrile; Anti Markovnikov; Electron deficient olefins; Sodium stannate; Solid superbase

Indexed keywords

ACRYLONITRILE; ANTI-MARKOVNIKOV; EFFICIENT CATALYSTS; ELECTRON-DEFICIENT OLEFINS; HIGH EFFICIENCY; HYDROALKOXYLATION; HYDROAMINATIONS; STANNATES; THERMAL TREATMENT;

CATALYSTS; ELECTRONS; HYDRATES; OLEFINS;

SODIUM;

EID: 78751648260     PISSN: 15667367     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.catcom.2010.12.030     Document Type: Article

References (32)

1. K. Tanabe, M. Misono, Y. Ono, and H. Hattori New Solid Acids and Bases, Their Catalytic Properties 1989 Kodansha Tokoy p. 3
2. X. Li, G.Z. Lu, Y.L. Guo, Y. Guo, Y.Q. Wang, Z.G. Zhang, X.H. Liu, and Y.S. Wang Catal. Commun. 8 2007 1969 1972
3. Y. Wang, W.Y. Huang, Y. Chun, J.R. Xia, and J.H. Zhu Chem. Mater. 13 2001 670 677
4. L.B. Sun, J. Yang, J.H. Kou, F.N. Gu, Y. Chun, Y. Wang, J.H. Zhu, and Z.G. Zou Angew. Chem. Int. Ed. 47 2008 3418 3421
5. H. Matsuhashi, M. Oikawa, and K. Arata Langmuir 16 2000 8201 8205
6. J. Kijeński, P. Radomski, and E. Fedoryńska J. Catal. 203 2001 407 425
7. H. Gorzawski, and W.F. Höelderich Appl. Catal. A Gen. 179 1999 131 137
8. R.M. Bota, K. Houthoofd, P.J. Grobet, and P.A. Jacobs Catal. Today 152 2010 99 103
9. J. Take, N. Kikuchi, and Y. Yoneda J. Catal. 21 1971 164 170
10. U. Meyer, H. Gorzawski, and W.F. Hölderich Catal. Lett. 59 1999 201 206
11. V.K. Díez, C.R. Apesteguía, and J.I. Di Cosimo J. Catal. 240 2006 235 244
12. M. Hayashi, K. Wada, and K. Munakata Agric. Biol. Chem. 47 1983 2653 2655
13. H. Kabbe, and A. Widdig Angew. Chem. Int. Ed. 21 1982 247 256
14. Y. Yamazaki, K. Abe, T. Toma, M. Nishikawa, H. Ozawa, A. Okuda, T. Araki, S. Oda, K. Inoue, K. Shibuya, B. Staels, and J. Fruchart Bioorg. Med. Chem. Lett. 17 2007 4689 4693
15. V. Cadierno, J. Francos, and J. Gimeno Chem. Eur. J. 14 2008 6601 6605
16. A. Ninagawu, and H. Matsuda Makromol. Chem. Rapid Commun. 2 1981 449 452
17. P.S. Manchand, P. Rosen, P.S. Belica, G.V. Oliva, A.V. Perrotta, and H.S. Wong J. Org. Chem. 57 1992 3531 3535
18. C. Munro-Leighton, E.D. Blue, and T.B. Gunnoe J. Am. Chem. Soc. 128 2006 1446 1447
19. J.H. MacGregor, and C. Pugh J. Chem. Soc. 1945 535 536
20. W.P. Uterrmohlen J. Am. Chem. Soc. 67 1945 1505 1506
21. H.L. Liu, H.F. Jiang, and Y.G. Wang Chin. J. Chem. 25 2007 1023 1026
22. A. Corma, and S. Iborra Adv. Catal. 49 2006 239 302
23. H. Kabashima, and H. Hattori Catal. Today 44 1998 277 283
24. H. Kabashima, and H. Hattori Appl. Catal. A Gen. 161 1997 L33 L35
25. P.S. Kumbhar, J. Sanchez-Valente, and F. Figueras Chem. Commun. 1998 1091 1092
26. O.D. Pavel, R. Bîrjega, M. Che, G. Costentin, E. Angelescu, and S. Şerban Catal. Commun. 9 2008 1974 1978
27. O.D. Pavel, R. Zǎvoianu, R. Bîrjega, and E. Angelescu Mater. Res. Bull. 45 2010 1106 1111
28. E. Angelescu, O.D. Pavel, M. Che, R. Bîrjega, and G. Constentin Catal. Commun. 5 2004 647 651
29. B.M. Choudary, M.L. Kantam, and B. Kavita Green Chem. 1999 289 292
30. M.J. Astle, and R.W. Etherington Ind. Eng. Chem. 44 1952 2871 2872
31. F. Guo, Z.G. Peng, J.Y. Dai, and Z.L. Xiu Fuel Process. Technol. 91 2010 322 328
32. H.W. Jiang, F. Hao, Q.Y. Chen, J.C. Xiao, S.B. Liu, and Y.C. Gu J. Org. Chem. 75 2010 3511 3514