Simple pyridylmethylamines: Efficient and robust N,N-ligands for Suzuki-Miyaura coupling reactions

Tetrahedron Letters

Volumn 51, Issue 41, 2010, Pages 5392-5394

  Gunawan, Maria Agatha ^a,b   Qiao, Chunjing ^a,b   Abrunhosa Thomas, Isabelle ^a,b   Puget, Bertrand ^a,b   Roblin, Jean Philippe ^a,b   Prim, Damien ^c   Troin, Yves ^a,b  

^a UNIVERSITÉ CLERMONT AUVERGNE   (France)

^b Ensemble Scientifique des Cézeaux   (France)

^c UNIVERSITÉ DE VERSAILLES SAINT QUENTIN EN YVELINES   (France)

Author keywords

N,N Ligands; Pyridylmethylamines; Suzuki Miyaura

Indexed keywords

LIGAND; METHYLAMINE; N,N BIDENDATE LIGAND; PALLADIUM; PYRIDYLMETHYLAMINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CHEMICAL BOND; SUZUKI REACTION; SYNTHESIS;

EID: 79961065644     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2010.07.151     Document Type: Article

References (28)

1. N. Miyaura, and A. Suzuki Chem. Rev. 95 1995 2457 2483
2. M. Miura Angew. Chem., Int. Ed. 43 2004 2201 2203
3. For recent review see: J.-P. Corbet, and G. Mignani Chem. Rev. 106 2006 2651 2710
4. For recent example see: P. Liu, M. Yan, and R. He Appl. Organomet. Chem. 24 2010 131 134
5. T. Mino, Y. Shirae, M. Sakamoto, and T. Fujita J. Org. Chem. 70 2005 2191 2194
6. For recent example see: A. da Conceiao Silva, J.S. Dias Senra, L.C. Sequeira, A.B.C. Simas, A.L.F. de Souza, L.F. Brum Malta, and O.A.C. Antunes Tetrahedron Lett. 51 2010 3883 3885
7. Y. Kitamura, S. Sako, A. Tsutsui, Y. Monguchi, T. Maegawa, Y. Kitade, and H. Sajiki Adv. Synth. Catal. 352 2010 718 730
8. A.E. Smith, K.M. Clapham, A.S. Batsanov, M.R. Bryce, and B. Tarbit Eur. J. Org. Chem. 2008 1458 1463
9. J.S. Siddle, A.S. Batsanov, and M.R. Bryce Eur. J. Org. Chem. 2008 2746 2750
10. O. Adidou, C. Goux-Henry, M. Safi, M. Soufiaoui, and E. Framery Tetrahedron Lett. 49 2008 7217 7219
11. P. Conelly-Espinosa, and D. Morales-Morales Inorg. Chim. Acta 363 2010 1311 1315
12. Y. Kitamura, A. Sakurai, T. Udzu, T. maegawa, Y. Monguchi, and H. Sajiki Tetrahedron 63 2007 10596 10602
13. I.V. Kuchurov, A.V. Vasil'ev, and S.G. Zlotin Mendeleev Commun. 20 2010 140 142
14. V. Cal, A. Nacci, A. Monopoli, and F. Montingelli J. Org. Chem. 70 2009 6040 6044
15. M. Lamblin, L. Nassar-Hardy, J.-C. Hierso, E. Fouquet, and F.-X. Felpin Adv. Synth. Catal. 352 2010 33 79
16. S. Shylesh, L. Wang, and W.R. Thiel Adv. Synth. Catal. 352 2010 425 432
17. E. Sin, S.-S. Yi, and Y.-S. Lee J. Mol. Catal. A 315 2010 99 104
18. E. Alacid, and C. Najera J. Organomet. Chem. 694 2009 1658 1665
19. S. Jana, S. Haldar, and S. Koner Tetrahedron Lett. 50 2009 4820 4823
20. D. Saha, K. Chattopadhyay, and B.C. Ranu Tetrahedron Lett. 50 2009 1003 1006
21. M.D. Astruc Inorg. Chem. 46 2007 1884 1894
22. Trilla, R. Pleixats, C. Bied, M. Wong Chi Man, and J.J. Moreau Tetrahedron Lett. 47 2006 2399 2403
23. S. Nishimura Handbook of Heterogeneous Catalytic Hydrogenation for Organic Synthesis 2001 Wiley-VCH New York, NY
24. For recent example see: A. Ohtaka, Y. Tamaki, Y. Igawa, K. Egami, O. Shimomura, and R. Nomura Tetrahedron 66 2010
25. For recent example see: J.L. Bolliger, and C.M. Frech Adv. Synth. Catal. 352 2010 1075 1080
26. V.F. Slagt, A.H.M. de Vries, J.G. de Vries, and R.M. Kellog Org. Process Res. Dev. 14 2010 30 47
27. B. Puget, J.-P. Roblin, D. Prim, and Y. Troin Tetrahedron Lett. 49 2008 1706 1709
28. V. Terrasson, D. Prim, and J. Marrot Eur. J. Inorg. Chem. 2008 2739 2745