PVC-supported palladium nanoparticles: An efficient catalyst for suzuki cross-coupling reactions at room temperature

Synthesis (Germany)

Volumn 45, Issue 9, 2013, Pages 1201-1206

  Samarasimhareddy, Mamidi ^a   Prabhu, Girish ^a   Vishwanatha, Thimmalapura M ^a   Sureshbabu, Vommina V ^a  

^a BANGALORE UNIVERSITY   (India)

Author keywords

biaryls; coupling reactions; halides; palladium; supported catalysis; Suzuki reactions

Indexed keywords

BIARYLS; COUPLING REACTION; HALIDES; SUPPORTED CATALYSIS; SUZUKI REACTION;

CATALYSIS; CATALYSTS; CHLORINE COMPOUNDS; NANOPARTICLES; ORGANIC SOLVENTS; POLYVINYL CHLORIDES;

PALLADIUM;

ALCOHOL; BENZENEBORONIC ACID; BIPHENYL DERIVATIVE; BROMIDE; CHLORIDE; IODIDE; IODOBENZENE; METAL NANOPARTICLE; PALLADIUM; PALLADIUM NANOPARTICLE; POLYVINYLCHLORIDE; UNCLASSIFIED DRUG; WATER;

ARTICLE; CATALYSIS; CONTROLLED STUDY; FILTRATION; GREEN CHEMISTRY; REACTION TIME; RECYCLING; ROOM TEMPERATURE; SUZUKI REACTION;

EID: 84876671883     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0033-1338293     Document Type: Article

References (28)

1. Handbook of Organopalladium Chemistry for Organic Synthesis. Negishi E., de Meijere A. Wiley New York: 2002
2. Johansson Seechurn C. C. C, Kitching M. O., Colacot T. J., Snieckus V. Angew. Chem. Int. Ed.: 2012; 51 5062
3. Miyaura N., Suzuki A. Chem. Rev.: 1995; 95 2457
4. Kohei T., Miyaura N. Top. Curr. Chem.: 2000; 219 1
5. Partyka D. V. Chem. Rev.: 2011; 111 1529
6. Miyaura N., Yamada K., Suzuki A. Tetrahedron Lett.: 1978; 3437
7. Yang J., Liu S., Zheng J.-F, Zhou J. Eur. J. Org. Chem.: 2012; 6248
8. Glasnov T. N., Kappe C. O. Adv. Synth. Catal.: 2010; 352 3089
9. Yin L., Liebscher J. Chem. Rev.: 2007; 107 133
10. Climent M. J., Corma A., Iborre S. Chem. Rev.: 2011; 111 1072
11. Roucoux A., Schultz J., Patin H. Chem. Rev.: 2002; 102 3757
12. Daniel M.-C, Astruc D. Chem. Rev.: 2004; 104 293
13. Baca A. J., Ahn J.-H, Sun Y., Meitl M. A., Menard E., Kim H.-S, Choi W. M., Kim D.-H, Huang Y., Rogers J. A. Angew. Chem. Int. Ed.: 2008; 47 5524
14. Crooks R. M., Zhao M., Sun L., Chechik V., Yeung L. K. Acc. Chem. Res.: 2001; 34 181
15. Prastaro A., Ceci P., Chiancone E., Boffi A., Cirilli R., Colone R. M., Fabrizi G., Stringaro A., Cacchi S. Green Chem.: 2009; 11 1929
16. Son S. U., Jang Y., Yoon K. Y., Kang E., Hyeon T. Nano Lett.: 2004; 4 1147
17. Zhang Z., Wang Z. J. Org. Chem.: 2006; 71 7485
18. Yan N., Zhang J.-g, Tong Y., Yao S., Xiao C., Li Z., Kou Y. Chem. Commun. (Cambridge): 2009; 4423
19. Hu Y., Yu Y., Hou Z., Li H., Zhao X., Feng B. Adv. Synth. Catal.: 2008; 350 2077
20. Favier I., Madec D., Teuma E., Gómez Curr. Org. Chem.: 2011; 15 3127
21. Astruc D. Inorg. Chem.: 2007; 46 1884
22. Kumar V. K. R, Sreedevi K., Gopidas K. R. Eur. J. Org. Chem.: 2012; 3447
23. Littke A. F., Dai C. Y., Fu G. C. J. Am. Chem. Soc.: 2000; 122 4020
24. Old D. W., Wolfe J. P., Buchwald S. L. J. Am. Chem. Soc.: 1998; 120 9722
25. Han W., Liu C., Jin Z. Adv. Synth. Catal.: 2008; 350 501
26. LeBlond C. R., Andrews A. T., Sun Y. K., Sowa J. R. Jr. Org. Lett.: 2001; 3 1555
27. Yin L., Zhang Z.-h, Wang Y.-m. Tetrahedron: 2006; 62 9359
28. Gallon B. J., Kojima R. W., Kaner R. B., Diaconescu P. L. Angew. Chem. Int. Ed.: 2007; 46 7251; Angew. Chem. 2007, 119, 7389