Tin(IV) hydrogen phosphate nanodisks: A mild and efficient catalyst for the protection of carbonyl compounds as 1,3-oxathiolanes

Catalysis Communications

Volumn 9, Issue 14, 2008, Pages 2398-2402

  Hazarika, Parasa ^a   Sharma, Saikat Das ^a   Konwar, Dilip ^a  

^a Synthetic Organic Chemistry Division   (India)

Author keywords

1,3 Oxathiolanes; Carbonyl compound; Heterogeneous catalyst; Nano disks; Sn(HPO4)2 H2O

Indexed keywords

ARSENIC COMPOUNDS; CARBONYLATION; CATALYSIS; CHLORINE COMPOUNDS; ELECTRON HOLOGRAPHY; HYDROGEN; NONMETALS; TITANIUM COMPOUNDS;

1,3-OXATHIOLANES; CARBONYL COMPOUND; CARBONYL COMPOUNDS; HETEROGENEOUS CATALYST; HETEROGENEOUS CATALYSTS; HYDROGEN PHOSPHATES; NANO DISKS;

TIN;

EID: 49149098257     PISSN: 15667367     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.catcom.2008.05.042     Document Type: Article

References (34)

1. Goldstein A.N. Handbook of Nanophase Materials (1997), Marcel Dekker, New York
2. Jin S., and Ye K. Biotechnol. Prog. 23 (2007) 32
3. Shenhar R., and Rotello V.M. Acc. Chem. Res. 36 (2003) 549
4. Wang Z., Zha Z., and Zhou C. Org. Lett. 4 (2002) 1683
5. Saxena A., Kumar A., and Majumdar S. Appl. Catal. A. Gen. 317 (2007) 210
6. Kidwai M., Bansal V., Saxena A., Aerry S., and Mazumdar S. Tetrahedron Lett. 47 (2006) 8049
7. Yan W., Wang R., Xu Z., Xu J., Lin L., Shen Z., and Zhou Y. J. Mol. Catal. A. 255 (2006) 81
8. Oyamada H., Akiyama R., Hagio H., Naito T., and Kobayashi S. Chem. Commun. (2006) 4297
9. Zhan B.-Z., White M.A., Sham T.-K., Pincock J.A., Doucet R.J., Ramana Rao K.V., Robertson K.N., and Cameron T.S. J. Am. Chem. Soc. 125 (2003) 2195
10. Park I.S., Kwon M.S., Kang K.Y., Lee J.S., and Park J. Adv. Synth. Catal. 349 (2007) 2039
11. Greene T.W., and Wuts P.G.M. Protective Group in Organic Synthesis. third ed. (1999), Wiley, New York Chapter 4
12. P.J. Kocienski, In Protective Groups, George Thieme, Stuttgart, 2000.
13. Lynch J.E., and Eliel E.J. J. Am. Chem. Soc. 106 (1984) 2943
14. Utimoto K., Nakamura A., and Molsubara S. J. Am. Chem. Soc. 112 (1990) 8189
15. Frye S.V., and Eliel E.L. Tetrahedron Lett. 26 (1985) 3907
16. Wilson Jr. G.E., Huang M.G., and Schloman Jr. W.W. J. Org. Chem. 33 (1968) 2133
17. Karimi B., and Seradj H. Synlett (2000) 805
18. Djerassi C., and Gorman M. J. Am. Chem. Soc. 75 (1953) 3704
19. Mondal E., Sahu P.R., and Khan A.T. Synlett (2002) 463
20. Chandrasekhar S., Prakash S.J., Shyamsunder T., and Ramachandar T. Synth. Commun. 35 (2005) 3127
21. Gogoi S., Borah J.C., and Barua N.C. Synlett (2004) 1592
22. Aoyama T., Takido T., and Kodomari M. Synlett (2004) 2307
23. Firouzabadi H., Iranpoor N., Jafari A.A., and Jafari M.R. J. Mol. Catal. A: Chem. (2006) 14
24. Ballini R., Bosica G., Maggi R., Mazzacani A., Righi P., and Sartori G. Synthesis (2001) 1826
25. Kazahaya K., Hamada N., and Ito S. Synlett (2002) 1535
26. De S.K. Tetrahedron Lett. 45 (2004) 2339
27. Rana K.K., Guin C., Jana S., and Roy S.C. Tetrahedron Lett. 44 (2003) 8597
28. Yadav J.S., Reddy B.V.S., and Kondaji G. Chem. Lett. 32 (2003) 672
29. Gogoi P., Sarmah G.K., and Konwar D. J. Org. Chem. 69 (2004) 5153
30. Gogoi P., Hazarika P., and Konwar D. J. Org. Chem. 70 (2005) 1934
31. Das Sharma S., Gogoi P., and Konwar D. Green Chem. 9 (2007) 153
32. Das Sharma S., Hazarika P., and Konwar D. Catal. Commun. 9 (2008) 709
33. Das Sharma S., Hazarika P., and Konwar D. Tetrahedron Lett. 49 (2008) 2216
34. Qiao H., Jia F., Ai Z., Li Z., and Zhang L. Chem. Commun. (2006) 2033