Palladium catalysed β-selective oxidative Heck reaction of an electron-rich olefin

Chemical Communications

Volumn 50, Issue 9, 2014, Pages 1110-1112

  Meng, Lingkui ^a   Liu, Chao ^a   Zhang, Wei ^a   Zhou, Chao ^a   Lei, Aiwen ^a,b  

^a WUHAN UNIVERSITY   (China)

^b JIANGXI NORMAL UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE; PALLADIUM; VINYL ACETATE;

ACIDITY; ARTICLE; ARYLATION; CATALYSIS; CONTROLLED STUDY; ELECTRON; HECK REACTION; SOLVENT EFFECT;

EID: 84891340898     PISSN: 13597345     EISSN: 1364548X     Source Type: Journal    
DOI: 10.1039/c3cc47045h     Document Type: Article

References (30)

1. R. F. Heck, J. Am. Chem. Soc., 1968, 90, 5535-5538
2. T. Mizoroki, K. Mori, A. Ozaki, Bull. Chem. Soc. Jpn., 1971, 44, 581
3. I. P. Beletskaya, A. V. Cheprakov, Chem. Rev., 2000, 100, 3009-3066
4. A. B. Dounay, L. E. Overman, Chem. Rev., 2003, 103, 2945-2964
5. W. Cabri, I. Candiani, Acc. Chem. Res., 1995, 28, 2-7
6. M. M. S. Andappan, P. Nilsson, H. von Schenck, M. Larhed, J. Org. Chem., 2004, 69, 5212-5218
7. J. Ruan, X. Li, O. Saidi, J. Xiao, J. Am. Chem. Soc., 2008, 130, 2424-2425
8. J. Ruan, J. Xiao, Acc. Chem. Res., 2011, 44, 614-626
9. M. Larhed, C.-M. Andersson, A. Hallberg, Tetrahedron, 1994, 50, 285-304
10. L. Xu, W. Chen, J. Ross, J. Xiao, Org. Lett., 2001, 3, 295-297
11. J. Mo, L. Xu, J. Xiao, J. Am. Chem. Soc., 2005, 127, 751-760
12. W. Pei, J. Mo, J. Xiao, J. Organomet. Chem., 2005, 690, 3546-3551
13. Z. Hyder, J. Mo, J. Xiao, Adv. Synth. Catal., 2006, 348, 1699-1704
14. J. Mo, J. Xiao, Angew. Chem., Int. Ed., 2006, 45, 4152-4157
15. L. R. Odell, J. Lindh, T. Gustafsson, M. Larhed, Eur. J. Org. Chem., 2010, 2270-2274
16. C. M. Andersson, A. Hallberg, J. Org. Chem., 1988, 53, 235-239
17. P. Nilsson, M. Larhed, A. Hallberg, J. Am. Chem. Soc., 2001, 123, 8217-8225
18. S. Chandrasekhar, C. Narsihmulu, S. S. Sultana, N. R. Reddy, Org. Lett., 2002, 4, 4399-4401
19. Y. C. Jung, R. K. Mishra, C. H. Yoon, K. W. Jung, Org. Lett., 2003, 5, 2231-2234
20. J. Tian, K. D. Moeller, Org. Lett., 2005, 7, 5381-5383
21. G. K. Datta, H. von Schenck, A. Hallberg, M. Larhed, J. Org. Chem., 2006, 71, 3896-3903
22. A. Trejos, A. Fardost, S. Yahiaoui, M. Larhed, Chem. Commun., 2009, 7587-7589
23. S. M. Bromidge, R. Arban, B. Bertani, M. Borriello, A.-M. Capelli, R. Di-Fabio, S. Faedo, M. Gianotti, L. J. Gordon, E. Granci, A. Pasquarello, S. K. Spada, A. Worby, L. Zonzini, V. Zucchelli, Bioorg. Med. Chem. Lett., 2010, 20, 7092-7096
24. V. Chandrasekhar, R. S. Narayanan, Tetrahedron Lett., 2011, 52, 3527-3531
25. Y. Terao, Y. Fukuoka, T. Satoh, M. Miura, M. Nomura, Tetrahedron Lett., 2002, 43, 101-104
26. R. Martín, S. L. Buchwald, Angew. Chem., Int. Ed., 2007, 46, 7236-7239
27. R. Martín, S. L. Buchwald, Org. Lett., 2008, 10, 4561-4564
28. G. D. Vo, J. F. Hartwig, Angew. Chem., Int. Ed., 2008, 47, 2127-2130
29. N. Chernyak, S. L. Buchwald, J. Am. Chem. Soc., 2012, 134, 12466-12469
30. M. Chen, J. Wang, Z. Chai, C. You, A. Lei, Adv. Synth. Catal., 2012, 354, 341-346