A new method for the synthesis of amides from imines

Tetrahedron Letters

Volumn 53, Issue 2, 2012, Pages 203-206

  Ghaffarzadeh, Mohammad ^a   Joghan, Somaye Shahrivari ^a   Faraji, Fereshteh ^a  

^a CHEMISTRY AND CHEMICAL ENGINEERING RESEARCH CENTER OF IRAN   (Iran)

Author keywords

Amide; Fentanyl; Imine; Reduction; Triethylsilane

Indexed keywords

ACID ANHYDRIDE; AMIDE; ANILINE; FENTANYL; IMINE; N (1 PHENETHYLPIPERIDIN 4 YLIDENE)ANILINE; SILANE DERIVATIVE; TRIETHYLSILANE; UNCLASSIFIED DRUG; ZINC;

ARTICLE; CHEMICAL REACTION; COLUMN CHROMATOGRAPHY; DRUG STRUCTURE; DRUG SYNTHESIS; PROTON NUCLEAR MAGNETIC RESONANCE;

EID: 83555177209     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2011.11.018     Document Type: Article

References (26)

1. F. Albericio Curr. Opin. Chem. Biol. 8 2004 211
2. G.S. Singh Tetrahedron 59 2003 7631
3. T. Cupido, J. Tulla-Puche, J. Spengler, and F. Alberico Curr. Opin. Drug Discov. Devel. 10 2007 768
4. J.W. Bode Curr. Opin. Drug Discov. Devel. 9 2006 765
5. I. Kobayashi, H. Muraoka, M. Hasegawa, T. Saika, M. Nishida, M. Kawamura, and R. Ando J. Antimicrob. Chemother. 50 2002 129
6. E. Aki-Sener, K.K. Bingol, I. Oren, O. Temiz-Arpaci, I. Yalcin, and N. Altanlar Farmaco 55 2000 469
7. K.J. Pradhan, P.S. Variyar, and J.R. Bandekar Lebensm Wiss. U. Technol. 32 1999 121
8. G.A. White Pestic. Biochem. Physiol. 34 1989 255
9. C.L. Allen, and J.M.J. Williams Chem. Soc. Rev. 40 2011 3405 and references cited therein
10. G. Benz B.M. Trost, I. Fleming, Comprehensive Organic Synthesis Vol. 6 1991 Pergamon Oxford 381 418
11. E. Valeur, and M. Bradley Chem. Soc. Rev. 38 2009 606
12. D.H. Cho, and D.O. Jang Tetrahedron Lett. 45 2004 2285
13. E.S. Kim, H.S. Lee, H.S. Kim, and J.N. Kim Tetrahedron Lett. 51 2010 1589
14. P. Theerthagiri, A. Lalitha, and P.N. Arunachalam Tetrahedron Lett. 51 2010 2813
15. L. Troisi, C. Granito, F. Rosato, and V. Videtta Tetrahedron Lett. 51 2010 371
16. J.S. Yadav, B.V. Subba Reddy, U.V. Subba Reddy, and K. Praneeth Tetrahedron Lett. 49 2008 4742
17. A. Shaabani, E. Soleimani, and A.H. Rezayan Tetrahedron Lett. 48 2007 6137
18. M. Sathishkumar, P. Shanmugavelan, S. Nagarajan, M. Maheswari, M. Dinesh, and A. Ponnuswamy Tetrahedron Lett. 52 2011 2830
19. F. Fazio, and C.-H. Wong Tetrahedron Lett. 44 2003 9083
20. G. Vasapollo, and H. Alper Tetrahedron Lett. 29 1988 5113
21. G. An, M. Kim, J.Y. Kim, and H. Rhee Tetrahedron Lett. 44 2003 2183
22. H. Shimizu, and S. Kobayashi Tetrahedron Lett. 46 2005 7593
23. U.A. Murashova, N.P. Sadchikova, L.V. Skalkina, and S.K. Smirnov Pharm. Chem. J. 38 2004 336
24. I.V. Mićović, M.D. Ivanović, S.M. Vuckovic, M.Š. Prostran, L. Doŝen-Mićović, and V.D. Kiricojević Bioorg. Med. Chem. Lett. 10 2000 2011
25. P.K. Gupta, K. Ganesan, A. Pande, and R.C. Malhotra J. Chem. Res. 2005 452
26. R. Vardanyan, G. Vijay, G.S. Nichol, L. Liu, I. Kumarasinghe, P. Davis, T. Vanderah, F. Porreca, J. Lai, and V.J. Hruby Bioorg. Med. Chem. 17 2009 5044