A concise synthetic approach towards hydroxytetraphenylenes

Synlett

Volumn , Issue 7, 2011, Pages 1018-1022

  Cui, Jian Fang ^a   Huang, Hui ^a   Wong, Henry N C ^a,b  

^a SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

^b CHINESE UNIVERSITY OF HONG KONG   (Hong Kong)

Author keywords

biaryls; copper; cross coupling; metalation; tetraphenylene

Indexed keywords

2,2' DIIODOBIPHENYL; ANILINE; BIPHENYL; COPPER; HYDROXYTETRAPHENYLENE; PHENAZONE; TETRAPHENYLENE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL ANALYSIS; CHEMICAL STRUCTURE; CROSS COUPLING REACTION; MOLECULAR DYNAMICS;

EID: 79954615436     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0030-1259708     Document Type: Article

References (28)

1. Rapson W S., Shuttleworth R G., Niekerk J N., J. Chem. Soc. 1943 326
2. Irngartinger H, Reibel W R. K., Acta Crystallogr., Sect. B: Struct. Sci. 1981 37 1724
3. Mak T C. W., Wong H N. C., In Comprehensive Supramolecular Chemistry Vol. 6 MacNicol D D. Toda F Bishop P Pergamon Press Oxford 1996 351
4. Mak T C. W., Wong H N. C., Top. Curr. Chem. 1987 140 141
5. Hou X.-L, Huang H, Wong H N. C., Synlett 2005 1073
6. Rajca A, Rajca S, Pink M, Miyasaka M, Synlett 2007 1799
7. Hisaki I, Sonoda M, Tobe Y, Eur. J. Org. Chem. 2006 833
8. Wang C, Xi Z, Chem. Commun. 2007 5119
9. Marsella M J., Rahbarnia S, Wilmot N, Org. Biomol. Chem. 2007 5 391
10. Huang H, Hau C.-K, Law C C. M., Wong H N. C., Org. Biomol. Chem. 2009 7 1249
11. Bachrach S M., J. Org. Chem. 2009 74 3609
12. Rajca A, Rajca S, Angew. Chem. Int. Ed. 2010 39 672
13. Wen J.-F, Hong W, Yuan K, Mak T C. W., Wong H N. C., J. Org. Chem. 2003 68 8918
14. Lai C W., Lam C K., Lee H K., Mak T C. W., Wong H N. C., Org. Lett. 2003 5 823
15. Hui C W., Mak T C. W., Wong H N. C., Tetrahedron 2004 60 3523
16. Peng H.-Y, Lam C.-K, Mak T C. W., Cai Z, Ma W.-T, Li Y.-X, Wong H N. C., J. Am. Chem. Soc. 2005 127 9603
17. Wu A.-H, Hau C.-K, Wong H N. C., Adv. Synth. Catal. 2007 349 601
18. Huang H, Stewart S, Gutmann M, Ohhara T, Niimura N, Li Y.-X, Wen J.-F, Bau R, Wong H N. C., J. Org. Chem. 2009 74 359
19. Rathore R, Magueres P L., Lindeman S V., Kochi J, Angew. Chem. Int. Ed. 2000 39 809
20. Rajca A, Wang H, Bolshov P, Rajca S, Tetrahedron 2001 57 3725
21. Kabir S M. H., Hasegawa M, Kuwatani Y, Yoshida M, Matsuyama H, Iyoda M, J. Chem. Soc., Perkin Trans. 1 2001 159
22. Shibata T, Chiba T, Hirashima H, Ueno Y, Endo K, Angew. Chem. Int. Ed. 2009 48 8066
23. Ooi T, Takahashi M, Yamada M, Tayama E, Omoto K, Maruoka K, J. Am. Chem. Soc. 2004 126 1150
24. Ferrer P, Avendaño C, Söllhuber M, Liebigs Ann. 1995 1895
25. Fourquez J M., Godard A, Marsais F, Quéguiner G, J. Heterocycl. Chem. 1995 32 1165
26. Seganish W M., DeShong P, J. Org. Chem. 2004 69 6790
27. Miyake Y, Wu M, Rahman J, Kuwatani Y, Iyoda M, J. Org. Chem. 2006 71 6110
28. Chan K L., Watkins S E., Mak C S. K., McKiernan M J., Towns C R., Pascu S I., Holmes A B., Chem. Commun. 2005 5766