Palladium on carbon-bromobenzene mediated esterification and transesterification

Tetrahedron Letters

Volumn 54, Issue 42, 2013, Pages 5690-5694

  Aavula, Sanjeev Kumar ^a   Chikkulapalli, Anil ^a   Hanumanthappa, N ^a   Jyothi, Indira ^a   Vinod Kumar, C H ^a   Manjunatha, Sulur G ^a  

^a ASTRAZENECA   (United Kingdom)

Author keywords

Bromobenzene; Esterification; Palladium; Transesterification

Indexed keywords

ALCOHOL DERIVATIVE; ALIPHATIC CARBOXYLIC ACID; AROMATIC CARBOXYLIC ACID; BROMOBENZENE; CARBON; HYDROBROMIC ACID; PALLADIUM;

ARTICLE; CATALYSIS; CHEMICAL ENVIRONMENT; HYDROGENATION; TRANSESTERIFICATION;

EID: 84883775046     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2013.08.009     Document Type: Article

References (38)

1. E. Fischer, and A. Speier Chem. Ber. 28 1895 3252
2. T.W. Greene, and P.G.M. Wuts Protective Groups in Organic Synthesis 3rd ed. 1999 Wiley New York
3. K. Ishihara, S. Ohara, and H. Yamamoto Tetrahedron 58 2002 8179
4. N. Bhatt, A. Patel, P. Selvam, and K.J. Sidhpuria Mol. Catal. 275 2007 14
5. A. Corma, H. Garcia, S. Iborra, and J. Primo J. Catal. 120 1989 78
6. J. Aracil, M. Martinez, N. Sanchez, and A. Corma Zeolites 12 1992 233
7. N. Sanchez, M. Martinez, J. Aracil, and A. Corma J. Am. Oil Chem. Soc. 69 1992 1150
8. E. Heykants, W.H. Verrelst, R.F. Parton, and P.A. Jacobs Stud. Surf. Sci. Catal. 105 1997 1277 1284
9. J. Inanaga, K. Hirata, H. Saeki, T. Katsuki, and M. Yamaguchi Bull. Chem. Soc. Jpn. 52 1979 1989 1993
10. O. Mitsunobu, and M. Yamada Bull. Chem. Soc. Jpn. 40 1967 2380 2382
11. O. Mitsunobu Synthesis 1981 1 28
12. K.C.K. Swamy, N.N.B. Kumar, E. Balaraman, and K.V.P.P. Kumar Chem. Rev. 109 2009 2551 2651
13. T. Yuen, S. Sze But, and P.H. Toy J. Am. Chem. Soc. 128 2006 9636 9637
14. E.A. Veliz, and P.A. Beal Tetrahedron Lett. 47 2006 3153 3156
15. A.M. Balint, A. Bodor, A. Gomory, K. Vkey, D. Szabo, and J. Rabai J. Fluorine Chem. 126 2005 1524 1530
16. D. Szabo, A.M. Bonto, I. Kovesdi, A. Gomory, and J. Rabai J. Fluorine Chem. 126 2005 641 652
17. A.M. Harned, H.S. He, P.H. Toy, D.L. Flynn, and P.R. Hanson J. Am. Chem. Soc. 127 2005 52 53
18. S. Dandapani, and D.P. Curran Chem. -Eur. J. 10 2004 3130 3138
19. R. Dembinski Eur. J. Org. Chem. 13 2004 2763 2772
20. S. Dandapani, and D.P. Curran Tetrahedron 58 2002 3855 3864
21. A.P. Dobbs, and C. McGregor-Johnson Tetrahedron Lett. 43 2002 2807 2810
22. J.C. Pelletier, and S. Kincaid Tetrahedron Lett. 41 2000 797 800
23. N. Iranpoor, H. Firouzabadi, D. Khalili, and S. Motevalli J. Org. Chem. 73 2008 4882 4887
24. S.P. Morcillo, L. Alvarez de, J.C. Antonio, M.J. Justicia, and R. Robles J. Org. Chem. 76 2011 2277 2281
25. J.S. Pizey Synthetic Reagents 1974 Horwood New York p 65
26. S.W. Fenton, A.E. DeWald, and R.T. Arnold J. Am. Chem. Soc. 77 1955 979 984
27. C.G. Overberger, and J.P. Anselme J. Org. Chem. 28 1963 592 593
28. S.T. Heller, and R. Sarpong Org. Lett. 12 2010 4572 4575
29. W. Pereira, V.A. Close, W. Patton, and B. Halpern J. Org. Chem. 34 1969 2032
30. Y. Masaki, N. Tanaka, and T. Miura Chem. Lett. 1997 55
31. B.C. Ranu, P. Dutta, and A. Sarkar J. Org. Chem. 63 1998 6027
32. B.C. Ranu, P. Dutta, and A. Sarkar Perkin Trans. 1 2000 2223
33. P. Baumhof, R. Mazitschek, and A. Giannis Angew. Chem., Int. Ed. 40 2001 3672
34. K. Ramalinga, P. Vijayalakshmi, and T.N.B. Kaimal Tetrahedron Lett. 43 2002 879
35. G.A. Grasa, R.M. Kissling, and S.P. Nolan Org. Lett. 4 2002 3583
36. G.W. Nyce, J.A. Lamboy, E.F. Connor, R.M. Waymouth, and J.L. Hedrick Org. Lett. 4 2002 3587
37. G.A. Grasa, T. Gueveli, R. Singh, and S.P. Nolan J. Org. Chem. 68 2003 2812
38. R. Singh, R.M. Kissling, M.A. Letellier, and S.P. Nolan J. Org. Chem. 69 2004 209