Beilstein J. Org. Chem. 2014, 10, 2892–2896.
19.Tobisu, M.; Chatani, N. Angew. Chem., Int. Ed. 2006, 45, 1683–1684.
24 h), the solvent was removed by evaporation and the residue
was purified by flash column chromatography on silica gel to
give N-arylpyrrole 3.
20.Pan, S. C. Beilstein J. Org. Chem. 2012, 8, 1374–1384.
21.Peng, B.; Maulide, N. Chem. – Eur. J. 2013, 19, 13274–13287.
Supporting Information
22.Haibach, M. C.; Seidel, D. Angew. Chem., Int. Ed. 2014, 53,
Supporting Information File 1
23.Verboom, W.; van Dijk, B. G.; Reinhoudt, D. N. Tetrahedron Lett. 1983,
24.Zhang, C.; Murarka, S.; Seidel, D. J. Org. Chem. 2009, 74, 419–422.
Experimental details, analytical data, and copies of the 1H
and 13C NMR spectra of the final products.
25.Mori, K.; Ohshima, Y.; Ehara, K.; Akiyama, T. Chem. Lett. 2009, 38,
26.Vadola, P. A.; Carrera, I.; Sames, D. J. Org. Chem. 2012, 77,
Acknowledgements
Financial support from the National Natural Science Founda-
tion of China (grants 81373303 and 81473080) is gratefully
acknowledged.
27.Mori, K.; Kawasaki, T.; Akiyama, T. Org. Lett. 2012, 14, 1436–1439.
28.He, Y.-P.; Wu, H.; Chen, D.-F.; Yu, J.; Gong, L.-Z. Chem. – Eur. J.
29.Pastine, S. J.; Sames, D. Org. Lett. 2005, 7, 5429–5431.
References
1. Godula, K.; Sames, D. Science 2006, 312, 67–72.
30.Jurberg, I. D.; Peng, B.; Wöstefeld, E.; Wasserloos, M.; Maulide, N.
Angew. Chem., Int. Ed. 2012, 51, 1950–1953.
3. Alberico, D.; Scott, M. E.; Lautens, M. Chem. Rev. 2007, 107,
31.Yan, R.-L.; Luo, J.; Wang, C.-X.; Ma, C.-W.; Huang, G.-S.; Liang, Y.-M.
32.Galliford, C. V.; Scheidt, K. A. J. Org. Chem. 2007, 72, 1811–1813.
4. Davies, H. M. L.; Manning, J. R. Nature 2008, 451, 417–424.
33.Jalal, S.; Sarkar, S.; Bera, K.; Maiti, S.; Jana, U. Eur. J. Org. Chem.
5. Chen, X.; Engle, K. M.; Wang, D.-H.; Yu, J.-Q. Angew. Chem., Int. Ed.
6. Jazzar, R.; Hitce, J.; Renaudat, A.; Sofack-Kreutzer, J.; Baudoin, O.
7. Lyons, T. W.; Sanford, M. S. Chem. Rev. 2010, 110, 1147–1169.
34.Pahadi, N. K.; Paley, M.; Jana, R.; Waetzig, S. R.; Tunge, J. A.
35.Deb, I.; Das, D.; Seidel, D. Org. Lett. 2011, 13, 812–815.
36.Ramakumar, K.; Tunge, J. A. Chem. Commun. 2014, 50,
8. Yu, J.-Q.; Shi, Z. Top. Curr. Chem. 2010, 292, 1–345.
37.Du, H.-J.; Zhen, L.; Wen, X.; Xu, Q.-L.; Sun, H. Org. Biomol. Chem.
9. Davies, H. M. L.; Du Bois, J.; Yu, J.-Q. Chem. Soc. Rev. 2011, 40,
10.Brückl, T.; Baxter, R. D.; Ishihara, Y.; Baran, P. S. Acc. Chem. Res.
License and Terms
11.Ackermann, L.; Vicente, R.; Kapdi, A. R. Angew. Chem., Int. Ed. 2009,
This is an Open Access article under the terms of the
Creative Commons Attribution License
12.Seregin, I. V.; Gevorgyan, V. Chem. Soc. Rev. 2007, 36, 1173–1193.
permits unrestricted use, distribution, and reproduction in
any medium, provided the original work is properly cited.
13.Daugulis, O.; Do, H.-Q.; Shabashov, D. Acc. Chem. Res. 2009, 42,
14.Cho, S. H.; Kim, J. Y.; Kwak, J.; Chang, S. Chem. Soc. Rev. 2011, 40,
15.Kuhl, N.; Hopkinson, M. N.; Wencel-Delord, J.; Glorius, F.
Angew. Chem., Int. Ed. 2012, 51, 10236–10254.
The license is subject to the Beilstein Journal of Organic
Chemistry terms and conditions:
16.Collet, F.; Dodd, R. H.; Dauban, P. Chem. Commun. 2009, 5061–5074.
17.Arockiam, P. B.; Bruneau, C.; Dixneuf, P. H. Chem. Rev. 2012, 112,
The definitive version of this article is the electronic one
which can be found at:
18.Jordan-Hore, J. A.; Johansson, C. C. C.; Gulias, M.; Beck, E. M.;
Gaunt, M. J. J. Am. Chem. Soc. 2008, 130, 16184–16186.
2896