Roomerature aerobic formation of a stable aryl-Cu(iii) complex and its reactions with nucleophiles: Highly efficient and diverse arene C-H functionalizations of azacalix[1]arene[3]pyridine

Chemical Communications

Volumn , Issue 20, 2009, Pages 2899-2901

  Yao, Bo ^a   Wang, De Xian ^a   Huang, Zhi Tang ^a   Wang, Mei Xiang ^a  

^a INSTITUTE OF GEOLOGY AND GEOPHYSICS   (China)

Author keywords

[No Author keywords available]

Indexed keywords

CALIXARENE; COPPER COMPLEX; NUCLEOPHILE; POLYCYCLIC AROMATIC HYDROCARBON; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE; PYRIDINE DERIVATIVE;

AEROBIC CAPACITY; ARTICLE; COMPLEX FORMATION; CRYSTAL STRUCTURE; MOLECULAR STABILITY; QUANTUM YIELD; REACTION TIME; ROOM TEMPERATURE; X RAY CRYSTALLOGRAPHY;

EID: 67449091161     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b902946j     Document Type: Article

References (36)

1. Handbook of C-H Transformations, ed., G. Dyker, Wiley-VCH Verlag GmbH & Co. KgaA, Weinheim, Germany, 2005
2. J. A. Labinger J. E. Bercaw Nature 2002 417 507
3. A. R. Dick M. S. Sanford Tetrahedron 2006 62 2439
4. B.-J. Li S.-D. Yang Z.-J. Shi Synlett 2008 947
5. A. R. Dick K. L. Hull M. S. Sanford J. Am. Chem. Soc. 2004 126 2300
6. W. C. P. Tsang N. Zheng S. L. Buchwald J. Am. Chem. Soc. 2005 127 14560
7. W. C. P. Tsang R. H. Munday G. Brasche N. Zheng S. L. Buchwald J. Org. Chem. 2008 73 7603
8. K. Inamoto C. Hasegawa K. Hiroya T. Doi Org. Lett. 2008 10 5147
9. X. Wan Z. Ma B. Li K. Zhang S. Cao S. Zhang Z. Shi J. Am. Chem. Soc. 2006 128 7416
10. G.-W. Wang T.-T. Yuan X.-L. Wu J. Org. Chem. 2008 73 4717
11. X. Chen X.-S. Hao C. E. Goodhue J.-Q. Yu J. Am. Chem. Soc. 2006 128 6790
12. G. Brasche S. L. Buchwald Angew. Chem., Int. Ed. 2008 47 1932
13. S. Ueda H. Nagasawa Angew. Chem., Int. Ed. 2008 47 6411
14. T. Uemura S. Imoto N. Chatani Chem. Lett. 2006 35 842
15. X. Ribas D. A. Jackon B. Donnadieu J. Mahia T. Parella R. Xifra B. Hedman K. O. Hodgson A. Llobet T. D. P. Stack Angew. Chem., Int. Ed. 2002 41 2991
16. R. Xifra X. Ribas A. Llobet A. Poater M. Duran M. Solà T. D. P. Stack J. Benet-Buchholz B. Donnadieu J. Mahía T. Parella Chem.-Eur. J. 2005 11 5146
17. L. M. Huffman S. S. Stahl J. Am. Chem. Soc. 2008 130 9196
18. M.-X. Wang Chem. Commun. 2008 4541
19. W. Maes W. Dehaen Chem. Soc. Rev. 2008 37 2393
20. H. Tsue K. Ishibashi R. Tamura Top. Heterocycl. Chem. 2008 17 73
21. B. König M. H. Fonseca Eur. J. Inorg. Chem. 2000 2303
22. N. Morohashi F. Narumi N. Iki T. Hattori S. Miyano Chem. Rev. 2006 106 5291
23. M. Vysotsky, K. Saadioui and V. Böhmer, in Calixarenes 2001, ed., Z. Asfarai, V. Böhmer, J. Harrowfield, and, J. Vicens, Kluwer, Dordrecht/Boston/London, 2001, pp. 250-265
24. M. Maekawa H. Konaka T. Minematsu T. Kuroda-Sowa M. Munakata S. Kitagawa Chem. Commun. 2007 5179
25. H.-Y. Gong X.-H. Zhang D.-X. Wang H.-W. Ma Q.-Y. Zheng M.-X. Wang Chem.-Eur. J. 2006 12 9262
26. H.-Y. Gong Q.-Y. Zheng X.-H. Zhang D.-X. Wang M.-X. Wang Org. Lett. 2006 8 4895
27. H.-Y. Gong D.-X. Wang J.-F. Xiang Q.-Y. Zheng M.-X. Wang Chem.-Eur. J. 2007 13 7791
28. S.-Q. Liu D.-X. Wang Q.-Y. Zheng M.-X. Wang Chem. Commun. 2007 3856
29. H.-Y. Gong D.-X. Wang Q.-Y. Zheng M.-X. Wang Tetrahedron 2009 65 87
30. M.-X. Wang H.-B. Yang J. Am. Chem. Soc. 2004 126 15412
31. B.-Y. Hou D.-X. Wang H.-B. Yang Q.-Y. Zheng M.-X. Wang J. Org. Chem. 2007 72 5218
32. H.-B. Yang D.-X. Wang Q.-Q. Wang M.-X. Wang J. Org. Chem. 2007 72 3757
33. B.-Y. Hou Q.-Y. Zheng D.-X. Wang Z.-T. Huang M.-X. Wang Chem. Commun. 2008 3864
34. Q.-Q. Wang D.-X. Wang Q.-Y. Zheng M.-X. Wang Org. Lett. 2007 9 2847
35. W. Van Rossom W. Maes L. Kishore M. Ovaere L. Van Meervelt W. Dehaen Org. Lett. 2008 10 585
36. D.-X. Wang Q.-Y. Zheng Q.-Q. Wang M.-X. Wang Angew. Chem., Int. Ed. 2008 47 7485