Copper-catalyzed cyanoalkylarylation of activated alkenes with AIBN: A convenient and efficient approach to cyano-containing oxindoles

RSC Advances

Volumn 4, Issue 89, 2014, Pages 48535-48538

  Wei, Wei ^a   Wen, Jiangwei ^a   Yang, Daoshan ^a   Guo, Mengyuan ^a   Tian, Laijin ^a   You, Jinmao ^a   Wang, Hua ^a  

^a QUFU NORMAL UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ACTIVATED ALKENES; OXINDOLES;

EID: 84907997109     PISSN: None     EISSN: 20462069     Source Type: Journal    
DOI: 10.1039/c4ra09022e     Document Type: Article

References (44)

1. B. Jacques and K. MuÇiz, in Catalyzed Carbon-Heteroatom Bond Formation, ed., A. K.Yudin, Wiley-VCH, Weinheim, 2010, p. 119
2. P. A. Sibbald, Palladium-catalyzed oxidative difunctionalization of alkenes: New reactivity and new mechanisms, ProQuest, UMI Dissertation Publishing, 2011
3. R. I. McDonald G. Liu S. S. Stahl Chem. Rev. 2011 111 2981
4. A. Minatti K. MuÇiz Chem. Soc. Rev. 2007 36 1142
5. K. H. Jensen M. S. Sigman Org. Biomol. Chem. 2008 6 4083
6. K. MuÇiz Angew. Chem., Int. Ed. 2009 48 9412
7. M.-B. Zhou R.-J. Song X.-H. Ouyang Y. Liu W.-T. Wei G.-B. Deng J.-H. Li Chem. Sci. 2013 4 2690
8. H. Wang L.-N. Guo X.-H. Duan Adv. Synth. Catal. 2013 355 2222
9. K. Matcha R. Narayan A. P. Antonchick Angew. Chem., Int. Ed. 2013 52 7985
10. X. H. Wei Y. Li A. X. Zhou T. T. Yang S. D. Yang Org. Lett. 2013 15 4158
11. J. Qiu R. Zhang Org. Biomol. Chem. 2014 12 4329
12. X. Li X. Xu P. Hu X. Xiao C. Zhou J. Org. Chem. 2013 78 7343
13. W. Wei J. Wen D. Yang J. Du J. You H. Wang Green Chem. 2014 16 2988
14. T. Shen Y. Yuan S. Song N. Jiao Chem. Commun. 2014 50 4115
15. X. Mu T. Wu H. Y. Wang Y. L. Guo G. S. Liu J. Am. Chem. Soc. 2012 134 878
16. H. Egami R. Shimizu S. Kawamura M. Sodeoka Angew. Chem., Int. Ed. 2013 52 4000
17. P. Xu J. Xie Q. C. Xue C. D. Pan Y. X. Cheng C. J. Zhu Chem.-Eur. J. 2013 19 14039
18. W. Kong M. Casimiro E. Merino C. Nevado J. Am. Chem. Soc. 2013 135 14480
19. W. Wei J. Wen D. Yang X. Liu M. Guo R. Dong H. Wang J. Org. Chem. 2014 79 4225
20. Y.-M. Li X.-H. Wei X.-A. Li S.-D. Yang Chem. Commun. 2013 49 11701
21. T. Shen Y. Z. Yuan N. Jiao Chem. Commun. 2014 50 554
22. Y.-M. Li M. Sun H.-L. Wang Q.-P. Tia S.-D. Yang Angew. Chem., Int. Ed. 2013 52 3972
23. J. Xie P. Xu H. Li Q. Xue H. Jin Y. Cheng C. Zhu Chem. Commun. 2013 49 5672
24. W.-T. Wei M.-B. Zhou J.-H. Fan W. Liu R.-J. Song Y. Liu M. Hu P. Xie J.-H. Li Angew. Chem., Int. Ed. 2013 52 3638
25. L.-N. Guo H. Wang X.-H. Duan Chem. Commun. 2013 49 7540
26. X. Xu Y. Tang X. Li G. Hong M. Fang X. Du J. Org. Chem. 2014 79 446
27. H. Lin S. J. Danishefsky Angew. Chem., Int. Ed. 2003 42 36
28. C. V. Galliford K. A. Scheidt Angew. Chem., Int. Ed. 2007 46 8748
29. R. Dalpozzo G. Bartoli G. Bencivenni Chem. Soc. Rev. 2012 41 7247
30. G. S. Singh Z. Y. Desta Chem. Rev. 2012 112 6104
31. K. Shen X. Liu L. Lin X. Feng Chem. Sci. 2012 3 327
32. L. Hong R. Wang Adv. Synth. Catal. 2013 355 1023
33. A. J. Fatiadi, in Preparation and Synthetic Applications of Cyano Compounds, ed., S.Patai, and, Z.Rappaport, Wiley, New York, 1983
34. R. C. Larock, Comprehensive Organic Transformations, VCH, New York, 1989
35. A. Pinto Y. Jia L. Neuville J. Zhu Chem.-Eur. J. 2007 13 961
36. Y. Yasui H. Kamisaki Y. Takemoto Org. Lett. 2008 10 3303
37. Y. Yasui H. Kamisaki T. Ishida Y. Takemoto Tetrahedron 2010 66 1980
38. H. Zhang P. Chen G. Liu Synlett 2012 23 2749
39. Y. Wu G. Liu Tetrahedron Lett. 2011 52 6450
40. T. Wu X. Mu G. Liu Angew. Chem., Int. Ed. 2011 50 12578
41. W. Wei C. Liu Da. Yang J. Wen J. You Y. Suo H. Wang Chem. Commun. 2013 49 10239
42. R. Spaccini N. Pastori A. Clerici C. Punta O. Porta J. Am. Chem. Soc. 2008 130 18018
43. M. N. C. Balili T. Pintauer Inorg. Chem. 2009 48 9018
44. M. N. C. Balili T. Pintauer Inorg. Chem. 2010 49 5642