Amino oxazolines as easily accessible water stable ligands for palladium catalysed aqueous Heck reaction

Journal of Chemical Research

Volumn 35, Issue 7, 2011, Pages 408-411

  Saiyed, Akeel S ^a   Joshi, Reshma S ^a   Bedekar, Ashutosh V ^a  

^a M S UNIVERSITY OF BARODA   (India)

Author keywords

Amino oxazolines; Heck reaction; palladium; water stable ligands

Indexed keywords

EID: 80051941911     PISSN: 03082342     EISSN: None     Source Type: Journal    
DOI: 10.3184/174751911X13100589976564     Document Type: Article

References (31)

1. R.F. Heck and J.P. Nolly, J. Org. Chem., 1972, 37, 2320.
2. T. Mizoroki, K. Mori and A. Ozaki, Bull. Chem. Soc. Jpn, 1971, 44, 581.
3. A. De Meijere and F.E. Meyer Angew. Chem., Int. Ed. Engl. 1994; 33: 2379.
4. W. Cabri, W. and I. Candiani, Acc. Chem. Res., 1995, 28, 2.
5. G.T. Crisp, Chem. Soc. Rev., 1998, 27, 427.
6. W.A. Hermann, K. Ofele, D. von Preysing and S.K. Schneider, J. Organomet. Chem., 2003, 687, 229.
7. V. Farina, Adv. Synth. Catal., 2004, 346, 1553.
8. W. Cabri, I. Candiani, A. Bedeschi, and R. Santi, J. Org. Chem., 1993, 58, 7421.
9. Q.-L. Zhou and A. Pfaltz, Tetrahedron, 1994, 50, 4407.
10. P. Braunstein and F Naud Angew. Chem., Int. Ed. Engl. 2001; 40: 680.
11. F Fache, E. Schulz, M.L. Tommasino and M. Lamaire, Chem. Rev., 2000, 100, 2159.
12. J.D. Senra, L.F.B. Malta, A.L.F. de Souza, M.E. Medeiros, L.C.S. Aguiar and O.A.C. Antunes, Tetrahedron Lett., 2007, 48, 8153.
13. B.H. Lipshutz and B.R. Taft, Org. Lett., 2008, 10, 1329.
14. S. Bhattacharya, A. Srivastava and S. Sengupta, Tetrahedron Lett., 2005, 46, 3557.
15. A.S. Gajare, N.S. Shaikh, G.K. Jnaneshwara, V.H. Deshpande, T. Ravindranathan, and A.V. Bedekar, J. Chem. Soc., Perkin Trans, 1 2000, 999.
16. S.A. Patel, K.N. Patel, S. Sinha, B.V. Kamath and A.V. Bedekar, J. Mol. Cat A: Chem., 2010, 332, 70.
17. T. Kawano, T. Shinomaru and I. Ueda, Org. Lett., 2002, 4, 2545.
18. R.B. Bedford, C.S.J. Cazin and D. Holder, Coord. Chem. Rev., 2004, 248, 2283.
19. C. Amatore and A. Jutand, Acc. Chem. Res., 2000, 33, 314.
20. Z. Zhang, Z. Zha, C. Gan, C. Pan, Y. Zhou. Z. Wang and M.-M. Zhou, J. Org. Chem., 2006, 71, 4339.
21. V.D. Filimonov, M. Trusova, P. Postnikov, E.A. Krasnokutskaya, Y.M. Lee, H.Y., Hwang, H. Kim and K.-W. Chi, Org. Lett., 2008, 10, 3961.
22. N. Duguet, A. Harrison-Marchand, J. Maddaluno and K. Tomioka Org. Lett., 2006, 8, 5745.
23. W.H. Laarhaoven, Th J.M. Cuppen and R.J.F. Niyard, Tetrahedron Lett., 1970, 26, 1069.
24. H. Marcel and S. Guy, J. Org. Chem., 1980, 45, 5393.
25. M.-S. Wu, D.K. Rayabarapu and C.-H. Cheng, J. Org. Chem., 2004, 69, 8407.
26. P. Wan, M.J. Davis and M.A. Teo, J. Org. Chem., 1989, 54, 1354.
27. A. Lansky, O. Reiser, O. and A. de Meijere, Synlett., 1990, 7, 405.
28. J.J. Heynekamp, W.M. Weber, L.A. Hunsaker, A.M. Gonzales, R.A. Orlando, L.M. Deck and L.M. Vander Jagt, J. Med. Chem., 2006, 49, 7182.
29. W. Bonarth, U. Letinois, T. Netscher and J. Schutz, Mizorok-Heck reaction, ed. M. Oestreich, A John-Wiley and Sons Ltd., West Sussex, 2009, pp. 495-521.
30. C. Bolm, K. Weickhardt, M. Zehnder and T. Ranff Chem. Ber., 1991, 124, 1173.
31. N. Romain, C. K. Jin, A.F. Coffey, J.W. Davies and M. Bradley Chem. Commun., 2007, 5031.