Solvent-free reactions of alkynes in ball mills: It is definitely more than mixing

Pure and Applied Chemistry

Volumn 83, Issue 7, 2011, Pages 1343-1349

  Stolle, Achim ^a   Ondruschka, Bernd ^a  

^a FRIEDRICH SCHILLER UNIVERSITY JENA   (Germany)

Author keywords

Alternative energy entry; Copper; Glaser reaction; Metal catalysis; Palladium; Sonogashira reaction

Indexed keywords

ALTERNATIVE ENERGY; GLASER REACTION; HOMOCOUPLING; METAL CATALYSIS; REACTION VARIABLES; SOLVENT FREE REACTION; SONOGASHIRA CROSS-COUPLING; SONOGASHIRA REACTIONS; TERMINAL ALKYNE; TURNOVER FREQUENCY; TURNOVER NUMBER;

ACETYLENE; BALL MILLING; CATALYSIS; MICROWAVE IRRADIATION; PALLADIUM; SOLVENTS;

BALL MILLS;

EID: 79959700649     PISSN: 00334545     EISSN: 13653075     Source Type: Journal    
DOI: 10.1351/PAC-CON-10-09-26     Document Type: Article

References (34)

1. R. A. Sheldon. Green Chem. 9, 1273 (2007).
2. T. Welton. Green Chem. 8, 13 (2006).
3. J. O. Metzger. Angew. Chem., Int. Ed. 37, 2975 (1998).
4. K. Tanaka, F. Toda. Chem. Rev. 100, 1025 (2000).
5. K. Tanaka. Solvent-Free Organic Synthesis, 2nd ed., Wiley-VCH, Weinheim (2009).
6. Organic Solid State Reactions in Top. Curr. Chem., F. Toda (Volume Ed.), Vol. 254, Springer, Berlin (2005).
7. G. Kaupp. J. Phys. Org. Chem. 21, 630 (2008).
8. G. Kaupp. In Solvent-Free Organic Synthesis, 2nd ed., K. Tanaka, pp. V-VI, Wiley-VCH, Weinheim (2009).
9. B. Rodriguez, A. Bruckmann, T. Rantanen, C. Bolm. Adv. Synth. Catal. 349, 2213 (2007).
10. R. Thorwirth, A. Stolle, B. Ondruschka. Green Chem. 12, 985 (2010).
11. Y. Liang, Y.-X. Xie, J.-H. Li. J. Org. Chem. 71, 379 (2006).
12. A. Carpita, A. Ribecai. Tetrahedron Lett. 50, 204 (2009).
13. D. A. Fulmer, W. C. Shearhouse, S. T. Medonza, J. Mack. Green Chem. 11, 1821 (2009).
14. M. Bandini, R. Luque, V. Budarin, D. J. Macquarrie. Tetrahedron 61, 9860 (2005).
15. Y.-X. Xie, C.-L. Deng, S.-F. Pi, J.-H. Li, D.-L. Yin. Chin. J. Chem. 24, 1290 (2006).
16. C.-L. Deng, Y.-X. Xie, D.-L. Yin, J. H. Li. Synthesis 3370 (2006).
17. M. Wang, P. Li, L. Wang. Synth. Commun. 34, 2803 (2004).
18. G. W. Kabalka, L. Wang, R. M. Pagni. Synlett 108 (2001).
19. A. Sharifi, M. Mirzaei, M. R. Naimi-Jamal. J. Chem. Res. 628 (2002).
20. A. Sharifi, M. Mirzaei, M. R. Naimi-Jamal. Chem. Monthly 137, 213 (2006).
21. D. Wang, J. Li, N. Li, T. Gao, S. Hou, B. Chen. Green Chem. 12, 45 (2010).
22. S. Feldbæk Nielsen, D. Peters, O. Axelsson. Synth. Commun. 30, 3501 (2000).
23. L. M. Klingensmith, N. E. Leadbeater. Tetrahedron Lett. 44, 765 (2003).
24. F. Schneider, B. Ondruschka. ChemSusChem 1, 622 (2008)
25. F. Schneider, A. Stolle, B. Ondruschka, H. Hopf. Org. Process Res. Dev. 13, 44 (2009).
26. R. Luque, D. J. Macquarrie. Org. Biomol. Chem. 7, 1627 (2009).
27. IUPAC. Compendium of Chemical Terminology, 2nd ed. (the "Gold Book"). Compiled by A. D. McNaught and A. Wilkinson. Blackwell Scientific Publications, Oxford (1997). XML on-line corrected version: doi:10.1351/goldbook (2006-) created by M. Nic, J. Jirat, B. Kosata; updates compiled by A. Jenkins (accessed 09-2010).
28. S. S. Palimkar, P. H. Kumar, N. R. Jogdand, T. Daniel, R. J. Lahoti, K. V. Srinivasan. Tetrahedron Lett. 47, 5527 (2006).
29. S. S. Palikmar, V. S. More, K. V. Srinivasan. Synth. Commun. 38, 1456 (2008).
30. F. Toda, Y. Tokumaru. Chem. Lett. 19, 987 (1990).
31. F. Schneider, T. Szuppa, A. Stolle, B. Ondruschka, H. Hopf. Green Chem. 11, 1894 (2009).
32. R. Trotzki, M. M. Hoffmann, B. Ondruschka. Green Chem. 10, 767 (2008).
33. R. Thorwirth, F. Bernhardt, A. Stolle, B. Ondruschka, J. Asghari. Chem.-Eur. J. 16, 13236 (2010).
34. L. Fomina, B. Vazquez, E. Tkatchouk, S. Fomine. Tetrahedron 58, 6741 (2002).