Facile and surfactant-free synthesis of Pd nanoparticles by the extract of the fruits of Piper longum and their catalytic performance for the Sonogashira coupling reaction in water under ligand- and copper-free conditions

RSC Advances

Volumn 5, Issue 4, 2015, Pages 2562-2567

  Nasrollahzadeh, Mahmoud ^a   Mohammad Sajadi, S ^b   Maham, Mehdi ^c   Ehsani, Ali ^a  

^a UNIVERSITY OF QOM   (Iran)

^b SORAN UNIVERSITY   (Iraq)

^c ISLAMIC AZAD UNIVERSITY   (Iran)

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSTS; CHELATION; COPPER; FRUITS; LIGANDS; NANOPARTICLES; SURFACE ACTIVE AGENTS;

AEROBIC CONDITION; CATALYTIC PERFORMANCE; COPPER-FREE SONOGASHIRA; COUPLING REACTION; HOMOGENEOUS CATALYST; PALLADIUM NANOPARTICLES; REACTION SOLUTIONS; SONOGASHIRA COUPLING REACTIONS;

SYNTHESIS (CHEMICAL);

EID: 84916888674     PISSN: None     EISSN: 20462069     Source Type: Journal    
DOI: 10.1039/c4ra12875c     Document Type: Article

References (36)

1. (a) K. Sonogashira, Y. Tohda and N. Hagihara, Tetrahedron Lett., 1975, 4467;
2. (b) M. Nasrollahzadeh, M. Khalaj and A. Ehsani, Tetrahedron Lett., 2014, 55, 5298;
3. (c) M. Nasrollahzadeh, M. Maham and M. M. Tohidi, J. Mol. Catal. A: Chem., 2014, 391, 83.
4. M. Nasrollahzadeh, S. M. Sajadi, A. Rostami-Vartooni and M. Khalaj, J. Mol. Catal. A: Chem., 2015, 396, 31.
5. E. Negishi and L. Anastasia, Chem. Rev., 2003, 103, 1979.
6. K. Sonogashira, in Comprehensive Organic Synthesis, ed. B. M. Trost and I. Fleming, Pergamon, New York, 1991, vol. 3.
7. S. Shylesh, V. Schunemann and W. R. Thiel, Angew. Chem., Int. Ed., 2010, 49, 3428.
8. C. Yi and R. Hua, Catal. Commun., 2006, 7, 377.
9. H. F. Chow, C. W. Wan, K. H. Low and Y. Y. Yeung, J. Org. Chem., 2001, 66, 1910.
10. A. Corma, H. Garciá and A. Primo, J. Catal., 2006, 241, 123.
11. B. Liang, M. Dai, J. Chen and Z. Yang, J. Org. Chem., 2005, 70, 391.
12. (a) M. B. Gawande, S. N. Shelke, R. Zboril and R. S. Varma, Acc. Chem. Res., 2014, 47, 1338;
13. (b) Y. Gu and G. Li, Adv. Synth. Catal., 2009, 351, 817;
14. (c) M. B. Gawande, P. S. Branco and R. S. Varma, Chem. Soc. Rev., 2013, 42, 3371;
15. (d) D. Wang and D. Astruc, Chem. Rev., 2014, 114(14), 6949.
16. D. Astruc, F. Lu and J. M. Aranzaes, Angew. Chem., Int. Ed., 2005, 44, 7852.
17. S. Wei, Z. Dong, Z. Ma, J. Sun and J. Ma, Catal. Commun., 2013, 30, 40.
18. Y. Konishi, K. Ohno, N. Saitoh, T. Nomura, S. Nagamine, H. Hishida, Y. Takahashi and T. Uruga, J. Biotechnol., 2007, 128, 648.
19. M. Rai, A. Yadav and A. Cade, Crit. Rev. Biotechnol., 2008, 28, 277.
20. S. S. Shankar, A. Ahmad and M. Sastry, Biotechnol. Prog., 2003, 19, 1627.
21. S. P. Dubey, M. Lahtinen and M. Sillanpa, Process Biochem., 2010, 45, 1065.
22. D. Philip, Spectrochim. Acta, Part A, 2009, 73, 374.
23. J. Kesharwani, J. K. Yoon, J. Hwang and M. Rai, J. Bionanosci., 2009, 3, 1.
24. V. K. Sharma, R. A. Yngard and Y. Lin, Adv. Colloid Interface Sci., 2009, 145, 83.
25. M. K. Santosh, D. Shaila, I. Rajyalakshmi and I. S. Rao, E-J. Chem., 2005, 2, 131.
26. S. Kumar, J. Kamboj and S. Sharma, J. Acupunct. Meridian Stud., 2011, 4, 134.
27. S. K. Madhu, V. A. Vijayan and A. K. Shaukath, Asian Pac. J. Trop. Biomed., 2011, 112.
28. N. Jayachandra Reddy, D. Nagoor Vali, M. Rani and S. Sudha Rani, Mater. Sci. Eng., C, 2014, 34, 115.
29. (a) M. Nasrollahzadeh, M. Maham, A. Ehsani and M. Khalaj, RSC Adv., 2014, 4, 19731;
30. (b) M. Nasrollahzadeh, A. Azarian, A. Ehsani and A. Zahraei, Tetrahedron Lett., 2014, 55, 2813;
31. (c) M. Nasrollahzadeh, M. Enayati and M. Khalaj, RSC Adv., 2014, 4, 26264;
32. (d) M. Nasrollahzadeh, F. Babaei, S. M. Sajadi and A. Ehsani, Spectrochim. Acta, Part A, 2014, 132, 423;
33. (e) P. Fakhri, B. Jaleh and M. Nasrollahzadeh, J. Mol. Catal. A: Chem., 2014, 383-384, 17;
34. (f) M. Nasrollahzadeh, A. Rostami-Vartooni, A. Ehsani and M. Moghadam, J. Mol. Catal. A: Chem., 2014, 387, 123;
35. (g) M. Nasrollahzadeh, S. M. Sajadi and M. Maham, J. Mol. Catal. A: Chem., 2015, 396, 297;
36. (h) M. Nasrollahzadeh, New J. Chem., 2014, 38, 5544.