Acidic ionic liquid [bmim]HSO4: An efficient catalyst for acetalization and thioacetalization of carbonyl compounds and their subsequent deprotection

Catalysis Communications

Volumn 8, Issue 9, 2007, Pages 1323-1328

  Gupta, Neeraj ^a   Sonu, ^a   Kad, Goverdhan L ^a   Singh, Jasvinder ^a  

^a PANJAB UNIVERSITY   (India)

Author keywords

Acetalization; Chemoselective; Ionic liquid; Microwave irradiation; Solvent free

Indexed keywords

ACETALIZATION; CARBONYL COMPOUNDS; DEPROTECTION; THIOACETALIZATION;

CARBONYLATION; IONIC LIQUIDS; MICROWAVE IRRADIATION; SULFUR COMPOUNDS; THERMAL EFFECTS;

CATALYSTS;

EID: 34447573702     PISSN: 15667367     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.catcom.2006.11.030     Document Type: Article

References (33)

1. Wasserscheid P., and Welton T. Ionic Liquids in Synthesis (2003), Wiley-VCH, Weinheim
2. Welton T. Coordin. Chem. Rev. 248 (2004) 2459
3. Wasserscheid P., and Keim W. Angew. Chem. Int. Ed. 39 (2000) 3772
4. Jain N., Kumar A., Chauhan S., and Chauhan S.M.S. Tetrahedron 61 (2005) 1015
5. Gu Y., Shi F., and Deng Y. J. Org. Chem. 69 (2004) 391
6. Anzalone P.W., and Mohan R.S. Synthesis (2005) 2661
7. Ranu B.C., and Jana R. J. Org. Chem. 70 (2005) 8621
8. Kim Y.J., and Varma R.S. J. Org. Chem. 70 (2005) 7882
9. Leadbeater N.E., and Torenius H.M. J. Org. Chem. 67 (2002) 3145
10. Whitehead J.A., Lawrance G.A., and McCluskey A. Green Chem. 6 (2004) 313
11. Singh V., Kaur S., Sapehiyia V., Singh J., and Kad G.L. Catal. Commun. 6 (2005) 57
12. Singh J., Gupta N., Kad G.L., and Kaur J. Synthetic Commun. 36 (2006) 2893
13. Greene T.W., and Watts P.G.M. Protective Groups in Organic Syntheses. second ed. (1991), Wiley, New York
14. Whitesell J.K. Chem. Rev. 89 (1989) 1581
15. Li D., Shi F., Peng J., Guo S., and Deng Y. J. Org. Chem. 69 (2004) 3582
16. Ott J., Tombo G.M.R., Schmid B., Venanzi L.M., Wang G., and Ward T.R. Tetrahedron Lett. 30 (1989) 6151
17. Yadav J.S., Subba Reedy B.V., Srinivas R., and Ramalingam T. Synlett (2000) 701
18. Mirjalili B.F., Zolfigol M.A., Bamoniri A., and Hazar A. J. Brazil Chem. Soc. 16 (2005) 877
19. Gopinath S.K.R., Haque J., and Patel B.K. J. Org. Chem. 67 (2002) 5842
20. Mirjalili B.F., Zolfigol M.A., Bamoniri A., Amrolahi M.A., and Hazar A. Phosphorus Sulfur 179 (2004) 1397
21. Bandgar B.P., and Gaikwad N.B. Monatsh. Chem. 129 (1998) 719
22. Das B., Ramu R., Reddy M.R., and Mahender G. Synthesis 2 (2005) 250
23. Ali M.H., and Gomes M.G. Synthesis (2005) 1326
24. Dong D., Ouyang Y., Yu H., Liu Q., Liu J., Wang M., and Zhu J. J. Org. Chem. 70 (2005) 4535
25. Burghardt T.E. J. Sulfur Chem. 26 (2005) 411
26. Carrigan M.D., Sarapa D., Smith R.C., Wieland L.C., and Mohan R.S. J. Org. Chem. 67 (2002) 1027
27. Mirjalili B.F., Zolfigol M.A., and Bamoniri A. Molecules 7 (2002) 751
28. Marko I., Ates A., Gautier A., Leroy B., Plancher J.M., Quesnel Y., and Vanherck J.C. Angew. Chem. Int. Ed. 38 (1999) 3207
29. Bailey A.D., Cherney S.M., Anzalone P.W., Anderson E.D., Ernat J.J., and Mohan R.S. Synlett (2006) 215
30. Yus M., Nájera C., and Foubelo F. Tetrahedron 59 (2003) 6147
31. Park J.H., and Kim S. Chem. Lett. (1989) 629
32. Firouzabadi H., Iranpoor N., Karimi B., and Hazarkhani H. Synlett (2000) 263
33. Tani H., Masumoto K., Inamasu T., and Suzuki H. Tetrahedron Lett. 32 (1991) 2039