Prins condensation for synthesis of nopol from β-pinene and paraformaldehyde on novel Fe-Zn double metal cyanide solid acid catalyst

Journal of Molecular Catalysis A: Chemical

Volumn 273, Issue 1-2, 2007, Pages 39-47

  Patil, Mallikarjun V ^a   Yadav, Mukesh K ^a   Jasra, Raksh V ^a  

^a CSIR CENTRAL SALT AND MARINE CHEMICALS RESEARCH INSTITUTE   (India)

Author keywords

pinene; Fe Zn double metal cyanide (DMC) complexes; Nopol; Prins condensation

Indexed keywords

BUTENES; CATALYSTS; CONDENSATION; FORMALDEHYDE; FOURIER TRANSFORM INFRARED SPECTROSCOPY; X RAY DIFFRACTION ANALYSIS;

NOPOL; PRINS CONDENSATION REACTION; SOLID ACID CATALYSTS;

NITROGEN COMPOUNDS;

EID: 34250798699     PISSN: 13811169     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molcata.2007.03.054     Document Type: Article

References (21)

1. Bain J.P. J. Am. Chem. Soc. 68 (1946) 638
2. Pillai U.R., and Demessie E.S. Chem. Commun. (2004) 826
3. Villa de P A.L., Alarcón E., and Monetes de C C. Chem. Commun. (2002) 2654
4. Villa de P A.L., Alarcón E., and Monetes de C C. Catal. Today 107-108 (2005) 942
5. Selvaraj M., and Kawi S. J. Mol. Catal. A: Chem. 246 (2006) 218
6. Yadav M.K., and Jasra R.V. Catal. Commun. 7 (2006) 891
7. Kim I., Yi M.J., Byun S.H., Park D.W., Kim B.U., and Ha C.S. Macromol. Symp. 224 (2005) 181
8. Srivastava R., Srinivas D., and Ratnasamy P. J. Catal. 241 (2006) 34
9. Sreeprasanth P.S., Srivastava R., Srinivas D., and Ratnasamy P. Appl. Catal. A: Gen. 314 (2006) 148
10. Liu H., Wang X., Gu Y., and Guo W. Molecules 8 (2003) 67
11. Chen S., Zhang P., and Chen L. Prog. Org. Coat. 50 (2004) 269
12. Nakamoto K. Infrared Spectra of Inorganic and Coordination Compounds (1963), John Wiley, New York p. 167
13. Kim I., Ahn J.T., Lee S.H., Ha C.S., and Park D.W. Catal. Today 93-95 (2004) 511
14. Kim I., Ahn J.T., Ha C.S., Yang C.S., and Park I. Polymer 44 (2003) 3417
15. M.O. James, L.L. Donald, L.G. Robin, US Patent 6,359,101 (2002).
16. K.G. McDaniel, M.J. Perry, J.E. Hayes, WO 9,914,258 (1999).
17. H. van der Hulst, G.A. Pogany, J. Kuyper, US Patent 4,477,589 (1984).
18. J. Milgrom, US Patent 3,404,109 (1968).
19. R.J. Herold, US Patent 3,278,459 (1966).
20. Darensbourg D.J., Adams M.J., and Yarbrough C. Inorg. Chem. 40 (2001)
21. Menini L., da Silva M.J., Lelis M.F.F., Fabris J.D., Lago R.M., and Gusevskaya E.V. Appl. Catal. A: Gen. 269 (2004) 117