Eco-efficiency and scalable synthesis of bisamides in deep eutectic solvent

Journal of Molecular Liquids

Volumn 206, Issue , 2015, Pages 268-271

  Azizi, Najmedin ^a   Alipour, Masoumeh ^a  

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

Author keywords

Aldehyde; Bisamide; Deep eutectic solvent; Green chemistry; Urea

Indexed keywords

ACCIDENT PREVENTION; ALDEHYDES; CHEMICAL INDUSTRY; CHLORINE COMPOUNDS; COST EFFECTIVENESS; ENVIRONMENTAL IMPACT; ENVIRONMENTAL MANAGEMENT; EUTECTICS; METABOLISM; UREA;

BISAMIDE; CHEMICAL PRODUCTION; DEEP EUTECTIC SOLVENTS; ENVIRONMENTAL PERFORMANCE; GREEN CHEMISTRY; LARGE SCALE PRODUCTIONS; SCALABLE SYNTHESIS; VOLATILE ORGANIC SOLVENTS;

SOLVENTS;

EID: 84924376642     PISSN: 01677322     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molliq.2015.02.033     Document Type: Article

References (36)

1. M. Lancaster Green Chemistry: An Introductory Text 2002 Royal Society of Chemistry Cambridge
2. A.S. Matlack Introduction to Green Chemistry 2001 Marcel Dekker New York
3. P.T. Anastas, and J.C. Warner Green Chemistry: Theory and Practice 1998 Oxford University Press Oxford
4. A.P. Abbott, G. Capper, D.L. Davies, R.K. Rasheed, and V. Tambyrajah Chem. Commun. 7 2003 70 71
5. Q. Zhang, K.D.O. Vigier, S. Royer, and F. Jérôme Chem. Soc. Rev. 41 2012 7108 7146
6. P. Wang, F.-P. Ma, and Z.-H. Zhang J. Mol. Liq. 198 2014 259 262
7. A. Hayyan, F.S. Mjalli, M.A. Hashim, M. Hayyan, I.M. AlNashef, S.M. Al-Zahrani, and M.A. Al-Saadi Bioresour. Technol. 102 2011 9564 9570
8. A. Hayyan, F.S. Mjalli, I.M. AlNashef, T. Al-Wahaibi, Y.M. Al-Wahaibi, and M.A. Hashim Thermochim. Acta 541 2012 70 75
9. A. Hayyan, M.A. Hashim, M. Hayyan, F.S. Mjalli, and I.M. AlNashef J. Clean. Prod. 65 2014 246 251
10. A.P. Abbott, R.C. Harris, K.S. Ryder, C. D'Agostino, L.F. Gladden, and M.D. Mantle Green Chem. 13 2011 82 90
11. S.B. Phadtare, K.J. Jarag, and G.S. Shankarling Dyes Pigments 97 2013 105 112
12. B.S. Singh, H.R. Lobo, D.V. Pinjari, K.J. Jarag, A.B. Pandit, and G.S. Shankarling Ultrason. Sonochem. 20 2013 633 639
13. F.S. Mjalli, J. Naser, B. Jibril, V. Alizadeh, and Z. Gano J. Chem. Eng. Data 59 2014 2242 2251
14. J. Parnica, and M. Antalik J. Mol. Liq. 197 2014 23 26
15. J. Ru, Y. Hua, J. Li, C. Xu, Y. Li, D. Wang, C. Qi, and Y. Jie J. Mol. Liq. 199 2014 208 214
16. A. Paiva, R. Craveiro, I. Aroso, M. Martins, R.L. Reis, and A.R.C. Duarte ACS Sustain. Chem. Eng. 2 2014 1063 1071
17. F. Monte, D. Carriazo, M.C. Serrano, M.C. Gutiérrez, and M.L. Ferrer ChemSusChem 7 2014 999 1009
18. W. Ailing, Z. Xueliang, Z. Zhuangzhi, L. Changping, and Z. Xuefang Prog. Chem. 26 2014 784 795
19. P. Li, F. Ma, P. Wang, and Z. Zhang Chin. J. Chem. 31 2013 757 763
20. E.E. Magat, B.F. Faris, J.E. Reith, and L.F. Salisbury J. Am. Chem. Soc. 73 1951 1028 1035
21. T.A. Ebel, A.A. Harwood, and A.M. Burkman J. Med. Chem. 10 1967 946 952
22. C. Vanier, A. Wagner, and C. Mioskowski Chem. Eur. J. 7 2001 2318 2325
23. Y. Zhang, Z. Zhong, Y. Han, R. Han, and X. Cheng Tetrahedron 69 2013 11080 11083
24. F. Tamaddon, H. Kargar-Shooroki, and A.A. Jafari J. Mol. Catal. A Chem. 369 2013 66 71
25. A.A. Bakibaev Russ. J. Org. Chem. 30 1994 1773 1775
26. V.K. Singh, H. Sharma, S.K. Singh, and L. Gangwar Chem. Biol. Drug Des. 82 2013 119 124
27. B.F. Mirjalili, and M.A. Mirhoseini J. Chem. Sci. 3 2013 1481 1486
28. A. Bayer, and M.E. Maier Tetrahedron 60 2014 6665 6672
29. Q. Wang, L. Sun, Y. Jiang, and C. Li Beilstein J. Org. Chem. 4 2008 51 59
30. M. Anary-Abbasinejad, M. Mosslemin, A. Hassanabadi, and S.T. Safa Synth. Commun. 40 2010 2209 2215
31. N. Azizi, and E. Batebi Catal. Sci. Technol. 2 2012 2445 2448
32. N. Azizi, E. Batebi, S. Bagherpour, and H. Ghafuri RSC Adv. 2 2012 2289 2293
33. N. Azizi, and E. Gholibeglo RSC Adv. 2 2012 7413 7416
34. N. Azizi, F. Ebrahimi, E. Aakbari, F. Aryanasab, and M.R. Saidi Synlett 2007 2797 2800
35. N. Azizi, A. Khajeh-Amiri, H. Ghafuri, M. Bolourtchian, and M.R. Saidi Synlett 2009 2245 2248
36. N. Azizi, and Z. Manocheri Res. Chem. Intermed. 38 2012 1495 1500