Ligand-free copper-catalyzed O-arylation of arenesulfonamides with phenols: An unusual approach to biaryl ether synthesis

References

• Evans, D. A.; Wood, M. R.; Trotter, B. W.; Richardson, T. I.; Barrow, J. C.; Katz, J. L. Angew. Chem. Int. Ed. Engl. 1998, 37, 2700-2704. DOI: 10.1002/(SICI)1521-3773(19981016)37:19<2700::AID-ANIE2700>3.0.CO;2-P.
   PubMed Web of Science ®Google Scholar
• Ley, S. V.; Thomas, A. W. Angew. Chem. Int. Ed. Engl. 2003, 42, 5400-5449. DOI: 10.1002/anie.200300594.
   PubMed Web of Science ®Google Scholar
• In, J.-K.; Lee, M.-S.; Yang, J.-E.; Kwak, J.-H.; Lee, H.; Boovanahalli, S. K.; Lee, K.; Kim, S. J.; Moon, S. K.; Lee, S.; et al. Bioorg. Med. Chem. Lett. 2007, 17, 1799-1802. DOI: 10.1016/j.bmcl.2006.12.048.
   PubMed Web of Science ®Google Scholar
• Zenitani, S.; Tashiro, S.; Shindo, K.; Nagai, K.; Suzuki, K.; Imoto, M.. J. Antibiot. 2003, 56, 617-621. DOI: 10.7164/antibiotics.56.617.
   PubMed Web of Science ®Google Scholar
• Beletskaya, I. P.; Cheprakov, A. V. Coord. Chem. Rev. 2004, 248, 2337-2764. DOI: 10.1016/j.ccr.2004.09.014.
   Web of Science ®Google Scholar
• Monnier, F.; Taillefer, M. Angew. Chem. Int. Ed. Engl. 2008, 47, 3096-3099. DOI: 10.1002/anie.200703209.
   PubMed Web of Science ®Google Scholar
• Ullmann, F. Ber. Dtsch. Chem. Ges. 1904, 37, 853-854. DOI: 10.1002/cber.190403701141.
   Google Scholar
• Wolfe, J. P.; Wagaw, S.; Marcoux, J.-F.; Buchwald, S. L. Acc. Chem. Res. 1998, 31, 805-818. DOI: 10.1021/ar9600650.
   Web of Science ®Google Scholar
• Shelby, Q.; Kataoka, N.; Mann, G.; Hartwig, J. J. Am. Chem. Soc. 2000, 122, 10718-10719. DOI: 10.1021/ja002543e.
   Web of Science ®Google Scholar
• Harkel, S.; Kumar, K.; Michalik, D.; Zapf, A.; Jackstell, R.; Rataboul, F.; Riemeier, T.; Monsees, A.; Beller, M. Tetrahedron Lett. 2005, 46, 3237-3240. DOI: 10.1016/j.tetlet.2005.03.033.
   Web of Science ®Google Scholar
• D.; Mann, G, B.; Hartwig, J. F. Curr. Org. Chem. 1997, 1, 287-305.
   Web of Science ®Google Scholar
• Marcoux, J.-F.; Doye, S.; Buchwald, S. L. J. Am. Chem. Soc. 1997, 119, 10539-10540. DOI: 10.1021/ja971901j.
   Web of Science ®Google Scholar
• Ma, D.; Cai, Q. Org. Lett. 2003, 5, 3799-3802. DOI: 10.1021/ol0350947.
   PubMed Web of Science ®Google Scholar
• Cai, Q.; Zou, B.; Ma, D. Angew. Chem. Int. Ed. Engl. 2006, 45, 1276-1279. DOI: 10.1002/anie.200503538.
   PubMed Web of Science ®Google Scholar
• Altman, R. A.; Buchwald, S. L. Org. Lett. 2007, 9, 643-646. DOI: 10.1021/ol062904g.
   PubMed Web of Science ®Google Scholar
• Lv, X.; Bao, W. J. Org. Chem. 2007, 72, 3863-3867. DOI: 10.1021/jo070443m.
   PubMed Web of Science ®Google Scholar
• Zhang, Q.; Wang, D.; Wang, X.; Ding, K. J. Org. Chem. 2009, 74, 7187-7190. DOI: 10.1021/jo9012157.
   PubMed Web of Science ®Google Scholar
• Tye, J. W.; Weng, Z.; Giri, R.; Hartwig, J. F. Angew. Chem. Int. Ed. Engl. 2010, 49, 2185-2189. DOI: 10.1002/anie.200902245.
   PubMed Web of Science ®Google Scholar
• Yong, F.-F.; Teo, Y.-C.; Yan, Y.-K.; Chua, G.-L. Synlett. 2012, 101-106.
   Web of Science ®Google Scholar
• Zheng, X.; Ding, J.; Chen, J.; Gao, W.; Liu, M.; Wu, H. Org. Lett. 2011, 13, 1726-1729. DOI: 10.1021/ol200251x.
   PubMed Web of Science ®Google Scholar
• Mondal, M.; Bharadwaj, S. K.; Bora, U. New J. Chem. 2015, 39, 31-37. DOI: 10.1039/C4NJ01293C.
   Web of Science ®Google Scholar
• Peng, D.; Yu, A.; Wang, H.; Wu, Y.; Chang, J. Tetrahedron 2013, 69, 6884-6889. DOI: 10.1016/j.tet.2013.05.112.
   Web of Science ®Google Scholar
• Chen, J.; Wang, X.; Zheng, X.; Ding, J.; Liu, M.; Wu, H. Tetrahedron 2012, 68, 8905-8907. DOI: 10.1016/j.tet.2012.08.032.
   Web of Science ®Google Scholar
• Phan, N. T. S.; Nguyen, T. T.; Nguyen, V. T.; Nguyen, K. D. ChemCatChem. 2013, 5, 2374-2381. DOI: 10.1002/cctc.201300032.
   Web of Science ®Google Scholar
• Wang, H.; Yu, A.; Cao, A.; Chang, J.; Wu, Y. Appl. Organomet. Chem. 2013, 27, 611-614.
   Web of Science ®Google Scholar
• Maity, T.; Bhunia, S.; Das, S.; Koner, S. RSC Adv. 2016, 6, 33380-33386. DOI: 10.1039/C6RA04409C.
   Web of Science ®Google Scholar
• Wenkert, E.; Ferreira, T. W.; Michelotti, E. L. J. Chem. Soc. Chem. Commun. 1979, 637-638. DOI: 10.1039/C39790000637.
   Google Scholar
• Okamura, H.; Miura, M.; Takei, H. Tetrahedron Lett. 1979, 20, 43-46. DOI: 10.1016/S0040-4039(01)85876-7.
   Google Scholar
• Clayden, J. J.; Cooney, A. Julia, J. Chem. Soc, Perkin Trans. 1 1995, 7-14. DOI: 10.1039/p19950000007.
   Google Scholar
• Cho, C.-H.; Yun, H.-S.; Park, K. J. Org. Chem. 2003, 69, 3017-3025. DOI: 10.1021/jo026449n.
   Google Scholar
• Milburn, R. R.; Snieckus, V. Angew. Chem. Int. Ed. 2004, 43, 888-891. DOI: 10.1002/anie.200352633.
   PubMed Web of Science ®Google Scholar
• Chen, J.; Zhang, K.; Zhao, Y.; Pu, S. Synth. Commun. 2018, 48, 1316-1323. DOI: 10.1080/00397911.2018.1441420.
   Web of Science ®Google Scholar
• Strieter, E. R.; Blackmond, D. G.; Buchwald, S. L. J. Am. Chem. Soc. 2005, 127, 4120-4121. DOI: 10.1021/ja050120c.
   PubMed Web of Science ®Google Scholar