Beilstein J. Org. Chem. 2017, 13, 1823–1827.
27.Takahashi, S.; Togo, H. Synthesis 2009, 2329.
References
1. Yoshimura, A.; Zhdankin, V. V. Chem. Rev. 2016, 116, 3328.
29.Schwekendiek, K.; Glorius, F. Synthesis 2006, 2996.
2. Zheng, Z.; Zhang-Negrerie, D.; Du, Y.; Zhao, K. Sci. China: Chem.
30.Asari, N.; Takemoto, Y.; Shinomoto, Y.; Yagyu, T.; Yoshimura, A.;
Zhdankin, V. V.; Saito, A. Asian J. Org. Chem. 2016, 5, 1314.
3. Zhdankin, V. V. Hypervalent Iodine Chemistry; Wiley: Chichester,
2014.
4. Zhdankin, V. V.; Stang, P. J. Chem. Rev. 2008, 108, 5299.
31.Saito, A.; Matsumoto, A.; Hanzawa, Y. Tetrahedron Lett. 2010, 51,
5. Brown, M.; Farid, U.; Wirth, T. Synlett 2013, 24, 424.
32.Senadi, G. C.; Guo, B.-C.; Hu, W.-P.; Wang, J.-J. Chem. Commun.
6. Yusubov, M. S.; Zhdankin, V. V. Resour.-Effic. Technol. 2015, 1, 49.
33.Liu, G.-Q.; Yang, C.-H.; Li, Y.-M. J. Org. Chem. 2015, 80, 11339.
8. Richardson, R. D.; Wirth, T. Angew. Chem., Int. Ed. 2006, 45, 4402.
34.Wang, N.; Chen, B.; Ma, S. Adv. Synth. Catal. 2014, 356, 485.
35.Senadi, G. C.; Hu, W.-P.; Hsiao, J.-S.; Vandavasi, J. K.; Chen, C.-Y.;
36.Hashmi, A. S. K.; Blanco Jaimes, M. C.; Schuster, A. M.; Rominger, F.
37.Minakata, S.; Morino, Y.; Oderaotoshi, Y.; Komatsu, M. Org. Lett. 2006,
9. Ochiai, M.; Takeuchi, Y.; Katayama, T.; Sueda, T.; Miyamoto, K.
10.Singh, F. V.; Wirth, T. Chem. – Asian J. 2014, 9, 950.
11.Romero, R. M.; Wöste, T. H.; Muñiz, K. Chem. – Asian J. 2014, 9, 972.
38.Gao, W.-C.; Hu, F.; Huo, Y.-M.; Chang, H.-H.; Li, X.; Wei, W.-L.
39.Bukšnaitienė, R.; Čikotienė, I. Synlett 2015, 26, 479.
12.Alhalib, A.; Kamouka, S.; Moran, W. J. Org. Lett. 2015, 17, 1453.
13.Rodríguez, A.; Moran, W. J. Org. Lett. 2011, 13, 2220.
40.Chao, M.; Hao, A.; Wang, H. Org. Process Res. Dev. 2009, 13, 645.
14.Rodríguez, A.; Moran, W. J. Synthesis 2012, 44, 1178.
41.Kaku, H.; Imai, T.; Kondo, R.; Mamba, S.; Watanabe, Y.; Inai, M.;
Nishii, T.; Horikawa, M.; Tsunoda, T. Eur. J. Org. Chem. 2013, 8208.
16.Parra, A.; Reboredo, S. Chem. – Eur. J. 2013, 19, 17244.
17.Liang, H.; Ciufolini, M. A. Angew. Chem., Int. Ed. 2011, 50, 11849.
18.Herkommer, D.; Thiede, S.; Wosniok, P. R.; Dreisigacker, S.; Tian, M.;
Debnar, T.; Irschik, H.; Menche, D. J. Am. Chem. Soc. 2015, 137,
License and Terms
This is an Open Access article under the terms of the
Creative Commons Attribution License
19.Bode, H. B.; Irschik, H.; Wenzel, S. C.; Reichenbach, H.; Müller, R.;
20.Célanire, S.; Wijtmans, M.; Christophe, B.; Collart, P.; de Esch, I.;
Dassesse, D.; Delaunoy, C.; Denonne, F.; Durieu, V.; Gelens, E.;
Gillard, M.; Lallemand, B.; Lamberty, Y.; Lebon, F.; Nicolas, J.-M.;
Quéré, L.; Snip, E.; Vanbellinghen, A.; Van houtvin, N.; Verbois, V.;
Timmerman, H.; Talaga, P.; Leurs, R.; Provins, L. ChemMedChem
permits unrestricted use, distribution, and reproduction in
any medium, provided the original work is properly cited.
The license is subject to the Beilstein Journal of Organic
Chemistry terms and conditions:
21.Celanire, S.; Talaga, P.; Leurs, R.; Denonne, F.; Timmerman, H.;
Lebon, F. Compounds comprising an oxazoline or thiazoline moiety,
processes for making them, and their uses. WO Patent
WO2006103057 A1, Oct 5, 2006.
The definitive version of this article is the electronic one
which can be found at:
22.Onishi, H. R.; Pelak, B. A.; Gerckens, L. S.; Silver, L. L.; Kahan, F. M.;
Chen, M.-H.; Patchett, A. A.; Galloway, S. M.; Hyland, S. A.;
Anderson, M. S.; Raetz, C. R. H. Science 1996, 274, 980.
23.Ilkgul, B.; Gunes, D.; Sirkecioglu, O.; Bicak, N. Tetrahedron Lett. 2010,
24.Brandstätter, M.; Roth, F.; Luedtke, N. W. J. Org. Chem. 2015, 80, 40.
25.Garg, P.; Chaudhary, S.; Milton, M. D. J. Org. Chem. 2014, 79, 8668.
26.Goud, D. R.; Pathak, U. Synthesis 2012, 44, 3678.
1827