References
- (a) Thansandote, P.; Lautens, M. Chem.-Eur. J. 2009, 15, 5874. https://doi.org/10.1002/chem.200900281
- Collet, F.; Dodd, R. H.; Dauban, P. Chem. Commun. 2009, 5061.
- (c) Cho, S. H.; Kim, J. Y.; Kwak, J.; Chang, S. Chem. Soc. Rev. 2011, 40, 5068. https://doi.org/10.1039/c1cs15082k
- (d) Samanta, R.; Matcha, K.; Antonchick, A. P. Eur. J. Org. Chem. 2013, 5769.
- (e) Louillat, M.-L.; Patureau, F. W. Chem. Soc. Rev. 2014, 43, 901. https://doi.org/10.1039/c3cs60318k
- Youn, S. W.; Bihn, J. H.; Kim, B. S. Org. Lett. 2011, 13, 3738. https://doi.org/10.1021/ol201416u
- Trost, B. M.; Dake, G. R. J. Am. Chem. Soc. 1997, 119, 7595. https://doi.org/10.1021/ja971238z
- (a) Abreu, A. S.; Silva, N. O.; Ferreira, P. M. T.; Queiroz, M.-J. R. P. Tetrahedron Lett. 2003, 44, 3377. https://doi.org/10.1016/S0040-4039(03)00564-1
- (b) Abreu, A. S.; Ferreira, P. M. T.; Queiroz, M.-J. R. P.; Ferreira, I. C. F. R.; Calhelha, R. C.; Estevinho, L. M. Eur. J. Org. Chem. 2005, 2951.
- (c) Stokes, B. J.; Dong, H.; Leslie, B. E.; Pumphrey, A. L.; Driver, T. G. J. Am. Chem. Soc. 2007, 129, 7500. https://doi.org/10.1021/ja072219k
- (d) Inamoto, K.; Saito, T.; Hiroya, K.; Doi, T. Synlett 2008, 3157.
- (e) Li, J.-J.; Mei, T.-S.; Yu, J.-Q. Angew. Chem. Int. Ed. 2008, 47, 6452. https://doi.org/10.1002/anie.200802187
- (f) Mei, T.-S.; Wang, X.; Yu, J.-Q. J. Am. Chem. Soc. 2009, 131, 10806. https://doi.org/10.1021/ja904709b
- (g) He, G.; Lu, C.; Zhao, Y.; Nack, W. A.; Chen, G. Org. Lett. 2012, 14, 2944. https://doi.org/10.1021/ol301352v
- (h) Mei, T.-S.; Leow, D.; Xiao, H.; Laforteza, B. N.; Yu, J.-Q. Org. Lett. 2013, 15, 3058. https://doi.org/10.1021/ol401246u
- (i) Inamoto, K.; Saito, T.; Katsuno, M.; Sakamoto, T.; Hiroya, K. Org. Lett. 2007, 9, 2931. https://doi.org/10.1021/ol0711117
- (j) Li, X.; He, L.; Chen, H.; Wu, W.; Jiang, H. J. Org. Chem. 2013, 78, 3636. https://doi.org/10.1021/jo400162d
- (k) Zhang, T.; Bao, W. J. Org. Chem. 2013, 78, 1317. https://doi.org/10.1021/jo3026862
- (l) Miura, M.; Tsuda, T.; Satoh, T.; Pivsa-Art, S.; Nomura, M. J. Org. Chem. 1998, 63, 5211. https://doi.org/10.1021/jo980584b
- (m) Inamoto, K.; Saito, T.; Hiroya, K.; Doi, T. J. Org. Chem. 2010, 75, 3900. https://doi.org/10.1021/jo100557s
- (n) Kim, B. S.; Lee, S. Y.; Youn, S. W. Chem. Asian J. 2011, 6, 1952. https://doi.org/10.1002/asia.201100024
- (o) Wang, L.; Guo, W.; Zhang, X.-X.; Xia, X.-D.; Xiao, W.-J. Org. Lett. 2012, 14, 740. https://doi.org/10.1021/ol203275b
- (a) Du, Y.; Liu, R.; Linn, G.; Zhao, K. Org. Lett. 2006, 8, 5919. https://doi.org/10.1021/ol062288o
- (b) Li, X.; Du, Y.; Liang, Z.; Li, X.; Pan, Y.; Zhao, K. Org. Lett. 2009, 11, 2643. https://doi.org/10.1021/ol9006663
- (c) Zheng, Y.; Li, X.; Ren, C.; Zhang-Negrerie, D.; Du, Y.; Zhao, K. J. Org. Chem. 2012, 77, 10353. https://doi.org/10.1021/jo302073e
Cited by
- Synthesis of Indole-2-carboxylate Derivatives via Palladium-Catalyzed Aerobic Amination of Aryl C–H Bonds vol.18, pp.15, 2016, https://doi.org/10.1021/acs.orglett.6b01592
- -Ts-Anilines and Styrenes vol.129, pp.23, 2017, https://doi.org/10.1002/ange.201702205
- Cross-Aldol Reaction of Activated Carbonyls with Nitrosocarbonyl Intermediates: Stereoselective Synthesis toward α-Hydroxy-β-amino Esters and Amides vol.19, pp.14, 2017, https://doi.org/10.1021/acs.orglett.7b01721
- -Ts-Anilines and Styrenes vol.56, pp.23, 2017, https://doi.org/10.1002/anie.201702205
- A Divergent Approach to Indoles and Oxazoles from Enamides by Directing-Group-Controlled Cu-Catalyzed Intramolecular C–H Amination and Alkoxylation vol.82, pp.17, 2017, https://doi.org/10.1021/acs.joc.7b01667
- Synthesis of indoles, indolines, and carbazoles via palladium-catalyzed C-H activation vol.2, pp.2, 2021, https://doi.org/10.1016/j.gresc.2021.02.001