In situ generated cetyltrimethylammonium bisulphate in choline chloride-urea deep eutectic solvent: A novel catalytic system for one pot synthesis of 1,3,4-oxadiazole

Catalysis Letters

Volumn 144, Issue 8, 2014, Pages 1393-1398

  More, Priyanka Anant ^a   Gadilohar, Balu Laxman ^a   Shankarling, Ganapati Subray ^a  

^a INSTITUTE OF CHEMICAL TECHNOLOGY   (India)

Author keywords

1,3,4 Oxadiazole; Acid hydrazide; Carboxylic acid; Cetyltrimethylammonium peroxodisulphate; Deep eutectic solvent

Indexed keywords

CARBOXYLIC ACIDS; CHLORINE COMPOUNDS; DEHYDRATION;

1 , 3 , 4-OXADIAZOLE; CATALYTIC SYSTEM; CETYLTRIMETHYLAMMONIUM; DEEP EUTECTIC SOLVENTS; ECO-FRIENDLY; ONE-POT SYNTHESIS; PEROXODISULPHATE; YIELDS OF PRODUCTS;

UREA;

EID: 84905574736     PISSN: 1011372X     EISSN: 1572879X     Source Type: Journal    
DOI: 10.1007/s10562-014-1288-3     Document Type: Article

References (35)

1. Nagaraj KC, Chaluvaraju MS, Niranajan SK (2011) Int J Pharm Pharm Sci 3:9
2. Khan RH, Rastogi RC (1990) J Agric Food Chem 38(4):1068
3. Li X, He D (2012) Dye Pigment 93:1422
4. Jin L, Chen J, Song B, Chen Z, Yang S, Li Q, Hu D, Xu R (2006) Bioorg Med Chem Lett 16:5036
5. Hokfelt B (1962) J Med Chem 5:247
6. Manjunatha K, Poojary B, Lobo P, Fernandes J, Kumari N (2010) Eur J Med Chem 45:5225
7. Adelstein G (1974) J Med Chem 16:309
8. Parameswaran M, Thengungal R, Gopalakrishnan S (2009) Acta Pharm 59:159
9. Patel K, Jayachandran E, Shah R, Javali V, Sreenivasa GM (2010) Int J Pharma Bio Sci 1:1
10. Zhou Y, Wang W, Dou W, Tang W, Liu W (2008) Chirality 20:110
11. Ding J, Day M, Robertson G, Roovers J (2002) Macromolecules 35:3474
12. Hughes G, Bryce MR (2005) J Mater Chem 15:94
13. Seo J, Kima S, Lee Y, Kwon O, Park K, Choi S, Chung Y, Jang D, Park S (2007) J Photochem Photobiol A 91:51
14. Dolman SJ, Gosselin F, O'Shea PD, Davies IW (2006) J Org Chem 71:9548
15. Katritzky AR, Mohapatra PP, Huang L (2008) ARKIVOC ix:62
16. Guin S, Ghosh T, Rout SK, Banerjee A, Patel BK (2011) Org Lett 13:5976
17. Reichart B, Kappe OC (2012) Tetrahedron Lett 53:952
18. Li C, Dickson HD (2009) Tetrahedron Lett 50:6435
19. Stabile P, Lamonica A, Ribecai A, Castoldi D, Guercio G, Curcuruto O (2010) Tetrahedron Lett 51:4801
20. Kangani CO, Kelley DE, Day BW (2006) Tetrahedron Lett 47:6497
21. Liras S, Allen MP, Segelstein BE (2000) Synth Commun 30:437
22. Bentiss F, Lagrenee M, Barbry D (2001) Synth Commun 31:935
23. Borg S, Estenne-Bouhtou G, Luthman K, Csoregh I, Hemelink W, Hacksell U (1995) J Org Chem 60:3112
24. Chandrakantha B, Isloor AM, Philip R, Mohesh M, Prakash S, Vijesh AM (2011) Bull Mater Sci 34:887
25. Abbott AP, Capper G, Davies DL, Rasheed RK, Tambyrajah V (2003) Chem Commun 1:70
26. Phadtare S, Shankarling G (2010) Green Chem 12:458
27. Singh B, Lobo H, Shankarling G (2011) Catal Lett 24:70
28. Gratzel CK, Jirousek M, Gratzel M (1984) J Phys Chem 88:1055
29. Tajbakhsh M, Alinezhad H, Urimi AG (2008) Phosphorus Sulfur Silicon Relat Elem 183:1447
30. Kumar P, Kumar A (2010) Bull Korean Chem Soc 31:2299
31. Wang W, Shao L, Cheng W, Yang J, He M (2008) Catal Commun 9:337
32. Urimi A, Alinezhad H, Tajbakhsh M (2008) Acta Chim Slovenica 55:481
33. Abbott AP, Davies DL, Capper G, Rasheed RK, Tambyrajah V (2007) US Patent 7,183,433
34. Firouzabadi H, Iranpoor N, Jafari AA, Riazymontazer E (2006) Adv Synth Catal 348:434
35. Xua X, Ye Q, Tang T, Wang D (2008) J Hazard Mater 158:410