Synthesis and applications of Fe3O4- diisopropylaminoacetamide as a versatile and reusable magnetic nanoparticle supported N,N-diisopropylethylamine equivalent

Tetrahedron Letters

Volumn 53, Issue 22, 2012, Pages 2689-2693

  Rattanaburi, Parintip ^a   Khumraksa, Bannarak ^a   Pattarawarapan, Mookda ^a  

^a CHIANG MAI UNIVERSITY   (Thailand)

Author keywords

H nig's base; Magnetic nanoparticles; N,N diisopropylethylamine; Solid supported reagent

Indexed keywords

3 AMINOPROPYLTRIETHOXYSILANE; ACETAMIDE DERIVATIVE; CHLORIDE; CHLORINE; IRON OXIDE; MAGNETIC NANOPARTICLE; SILICON DIOXIDE; TRIAZINE DERIVATIVE;

ACYLATION; ALKYLATION; CHEMICAL MODIFICATION; MAGNET; MATERIAL COATING; NANOFABRICATION; REVIEW; SULFONATION; SURFACE PROPERTY; SYNTHESIS;

EID: 84860225048     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2012.03.063     Document Type: Article

References (31)

1. J.L. Moore, S.M. Taylor, and V.A. Soloshonok ARKIVOC 6 2005 287 292
2. K.M. Sivanandaiah, V.V.S. Babu, and C. Renukeshwar Int. J. Pept. Prot. Res. 39 1992 201 206
3. J. Fu, and S.J. Shuttleworth Tetrahedron Lett. 44 2003 3843 3845
4. A. Ryckebusch, R. Deprez-Poulain, M.A. Debreu-Fontaine, R. Vandaele, E. Mouray, P. Grellier, and C. Sergheraert Bioorg. Med. Chem. Lett. 12 2002 2595 2598
5. M. Beyermann, P. Henklein, A. Klose, R. Sohr, and M. Bienert Int. J. Pept. Prot. Res. 37 1991 252 256
6. D.H. Drewry, D.M. Coe, and S. Poon Med. Res. Rev. 19 1999 97 148
7. A. Solinas, and M. Taddei Synthesis 2007 2409 2453
8. R. Mello, A. Alcalde-Aragones, and M.E. Gonzalez-Nunez Tetrahedron Lett. 51 2010 4281 4283
9. A.R. Modarresi-Alam, F. Khamooshi, M. Nasrollahzadeh, and H.A. Amirazizi Tetrahedron 63 2007 8723 8726
10. C. Wiles, P. Watts, and S.J. Haswell Tetrahedron Lett. 47 2006 5261 5264
11. E. Gershonov, I. Columbus, and Y. Zafrani J. Org. Chem. 74 2009 329 338
12. N.C. Ganguly, P. De, A.K. Sukai, and S. De Synth. Commun. 32 2002 1 7
13. R.S. Varma Tetrahedron 58 2002 1235 1255
14. V. Polshettiwar, R. Luque, A. Fihri, H. Zhu, M. Bouhrara, and J.M. Basset Chem. Rev. 111 2011 3036 3075
15. K.I. Fujita, S. Umeki, M. Yamazaki, T. Ainoya, T. Tsuchimoto, and H. Yasuda Tetrahedron Lett. 52 2011 3137 3140
16. J. Deng, L.P. Mo, F.Y. Zhao, L.L. Hou, L. Yang, and Z.H. Zhang Green Chem. 13 2011 2576 2584
17. A. Bee, R. Massart, and S. Neveu J. Magn. Magn. Mater. 149 1995 6 9
18. R.V. Ferreira, I.L.S. Pereira, L.C.D. Cavalcante, L.F. Gamarra, S.M. Carneiro, E. Amaro Jr, J.D. Fabris, R.Z. Domingues, and A.L. Andrade Hyperfine Interact. 195 2009 265 274
19. M. Pattarawarapan, and S. Singhatana Chiang Mai J. Sci. 33 2006 203 209
20. J.D. Moore, R.H. Herpel, J.R. Lichtsinn, D.L. Flynn, and P.R. Hanson Org. Lett. 5 2003 105 107
21. M. Jafarpour, A. Rezaeifard, and M. Aliabadi Appl. Catal., A 358 2009 49 53
22. A.R. Massah, F. Kazemi, D. Azadi, S. Farzaneh, H. Aliyan, H.J. Naghash, and A.R. Momeni Lett. Org. Chem. 3 2006 235 241
23. M.S.R. Murty, N.R. Reddy, and J.S. Yadav J. Sulfur Chem. 27 2006 589 593
24. A. Rolfe, D.A. Probst, K.A. Volp, I. Omar, D.L. Flynn, and P.R. Hanson J. Org. Chem. 73 2008 8785 8790
25. L.Q. Kang, Y.Q. Cai, Y.Q. Peng, X.L. Ying, and G.H. Song Mol. Diversity 15 2011 109 113
26. Y. Li, Y. Zhao, Z. Zhang, and Y. Xu Tetrahedron Lett. 51 2010 1434 1436
27. M. Lei, X.L. Tao, and Y.G. Wang Helv. Chim. Acta 89 2006 532 536
28. M. Figlus, A.C. Tarruella, A. Messer, S.L. Sollis, and R.C. Hartley Chem. Commun. 46 2010 4405 4407
29. M.B. Gawande, S.S. Deshpande, J.R. Satam, and R.V. Jayaram Catal. Commun. 8 2007 576 582
30. F. Cardullo, D. Donati, V. Fusillo, G. Merlo, A. Paio, M. Salaris, A. Solinas, and M. Taddei J. Comb. Chem. 8 2006 834 840
31. R.N. Salvatore, A.S. Nagle, and W.J. Kyung J. Org. Chem. 67 2002 674 683