[1] (a) McGrath, N. A.; Brichacek, M.; Njardarson, J. T. J. Chem. Educ. 2010, 87, 1348.
(b) Barreiro, E. J.; Kummerle, A. E.; Fraga, C. A. Chem. Rev. 2011, 111, 5215.
[2] For an example, see:Angell, R.; Aston, N. M.; Bamborough, P.; Buckton, J. B.; Cockerill, S.; deBoeck, S. J.; Edwards, C. D.; Holmes, D. S.; Jones, K. L.; Laine, D. I.; Patel, S.; Smee, P. A.; Smith, K. J.; Somers, D. O.; Walker, A. L. Bioorg. Med. Chem. Lett. 2008, 18, 4428.
[3] (a) Schönherr, H.; Cernak, T. Angew. Chem., Int. Ed. 2013, 52, 12256.
(b) Leung, C. S.; Leung, S. S. F.; Tirado-Rives, J.; Jorgensen, W. L. J. Med. Chem. 2012, 55, 4489.
[4] For selected recent examples, see:(a) Feng, K.; Quevedo, R. E.; Kohrt, J. T.; Oderinde, M. S.; Reilly, U.; White, M. C. Nature 2020, 580, 621.
(b) Serpier, F.; Pan, F.; Ham, W. S.; Jacq, J.; Genicot, C.; Ritter, T. Angew. Chem., Int. Ed. 2018, 57, 10697.
(c) Haydl, A. M.; Hartwig, J. F. Org. Lett. 2019, 21, 1337.
(d) Ye, W.; Yan, Z.; Wan, C.; Hou, H.; Wang, Z. Acta Chim. Sinica 2018, 76, 99(in Chinees). (叶文波, 晏子聪, 万常峰, 侯豪情, 汪志勇, 化学学报, 2018, 76, 99.)
[5] (a) Minisci, F.; Bernardi, R.; Bertini, F.; Galli, R.; Perchinummo, M. Tetrahedron 1971, 27, 3575.
(b) Ochiai, M.; Morita, K. Tetrahedron Lett. 1967, 8, 2349.
(c) Minisci, F.; Galli, R.; Cecere, M.; Malatesta, V.; Caronna, T. Tetrahedron Lett. 1968, 9, 5609.
(d) Sugimori, A.; Yamada, T.; Ishida, H.; Nose, M.; Terashima, K.; Oohata, N. Bull. Chem. Soc. Jpn. 1986, 59, 3905.
[6] For reviews of methylation methods, see:(a) Yan, G.; Borah, A. J.; Wang, L.; Yang, M. Adv. Synth. Catal. 2015, 357, 1333.
(b) Kim, J.; Cho, S. H. Synlett 2016, 27, 2525.
(c) Hu, L.; Liu, Y. A.; Liao, X. Synlett 2018, 29, 375.
[7] For selected examples, see:(a) Hu, L.; Liu, X.; Liao, X. Angew. Chem., Int. Ed. 2016, 55, 9743.
(b) Yang, C. T.; Zhang, Z. Q.; Liu, Y. C.; Liu, L. Angew. Chem., Int. Ed. 2011, 50, 3904.
(c) Agrawal, T.; Cook, S. P. Org. Lett. 2014, 16, 5080.
(d) Shang, R.; Ilies, L.; Nakamura, E. J. Am. Chem. Soc. 2015, 137, 7660.
(e) Wang, J.; Zhao, J.; Gong, H. Chem. Commun. 2017, 53, 10180.
(f) Liang, Z.; Xue, W.; Lin, K.; Gong, H. Org. Lett. 2014, 16, 5620.
(g) Shi, W.-J.; Shi, Z.-J. Chin. J. Chem. 2018, 36, 183.
[8] Uemura, T.; Yamaguchi, M.; Chatani, N. Angew. Chem., Int. Ed. 2016, 55, 3162.
[9] He, Z.-T.; Li, H.; Jaudl, A. M.; Whiteker, G. T.; Hartwig, J. F. J. Am. Chem. Soc. 2018, 140, 17197.
[10] Huihui, K. M. M.; Caputo, J. A.; Melchor, Z.; Olivares, A. M.; Spiewak, A. M.; Johnson, K. A.; DiBenedetto, T. A.; Kim, S.; Ackerman, L. K. G.; Weix, D. J. J. Am. Chem. Soc. 2016, 138, 5016.
[11] Kariofillis, S. K.; Shields, B. J.; Tekle-Smith, M. A.; Zacuto, M. J.; Doyle, A. G. J. Am. Chem. Soc. 2020, 142, 7683.
[12] (a) Xiao, Q.; Zhang, Y.; Wang, J. Acc. Chem. Res. 2013, 46, 236.
(b) Xia, Y.; Qiu, D.; Wang, J. Chem. Rev. 2017, 117, 13810.
(c) Xia, Y.; Wang, J. J. Am. Chem. Soc. 2020, 142, 10592.
[13] For selected examples for reductive coupling reactions involving metal carbene species, see:(a) Xia, Y.; Hu, F.; Liu, Z.; Qu, P.; Ge, R.; Ma, C.; Zhang, Y.; Wang, Org. Lett. 2013, 15, 1784.
(b) Xia, Y.; Hu, F.; Xia, Y.; Liu, Z.; Ye, F.; Zhang, Y.; Wang, J. Synthesis 2017, 49, 1073.
[14] For the examples of using TMSCHN2 in cross-coupling reactions, see:(a) Kudirka, R.; Van Vranken, D. L. J. Org. Chem. 2008, 73, 3585.
(b) Xu, S.; Chen, R.; Fu, Z.; Zhou, Q.; Zhang, Y.; Wang, J. ACS Catal. 2017, 7, 1993.
[15] (a) Leiendecker, M.; Hsiao, C.-C.; Guo, L.; Alandini, N.; Rueping, M. Angew. Chem., Int. Ed. 2014, 53, 12912.
(b) Zhang, W.-X.; Ding, C.-H.; Luo, Z.-B.; Hou, X.-L.; Dai, L.-X. Tetrahedron Lett. 2006, 47, 8391.
(c) Baciocchi, E.; Rol, C.; Rosato, G. C.; Sebastiani, G. V. J. Chem. Soc., Chem. Commun. 1992, 59.
[16] (a) Cai, G.; Huang, Y.; Du, T.; Zhang, S.; Yao, B.; Li, X. Chem. Commun. 2016, 52, 5425.
(b) Perez, I.; Sestelo, J. P.; Sarandeses, L. A. J. Am. Chem. Soc. 2001, 123, 4155.
[17] Mu, Q.-C.; Wang, X.-B.; Ye, F.; Sun, Y.-Li.; Bai, X.-F.; Chen, J.; Xia, C.-G.; Xu, Li.-W. Chem. Commun. 2018, 54, 12994.
[18] Tobisu, M.; Kita, Y.; Ano, Y.; Chatani, N. J. Am. Chem. Soc. 2008, 130, 15982.
[19] Suzuki, H.; Murashima, T.; Kozai, I.; Mori, T. J. Chem. Soc., Perkin Trans. 11993, 1591.
[20] Molander, G. A.; Yun, C.-S.; Ribagorda, M.; Biolatto, B. J. Org. Chem. 2003, 68, 5534.
[21] Das, M.; O'Shea, D. F. Tetrahedron 2013, 69, 6448.
[22] Kalvet, I.; Sperger, T.; Scattolin, T.; Magnin, G.; Schoenebeck, F. Angew. Chem., Int. Ed. 2017, 56, 7078.
[23] Wu, Y.; Bouvet, S.; Izquierdo, S.; Shafir, A. Angew. Chem., Int. Ed. 2019, 58, 2617.
[24] Heijnen, D.; Hornillos, V.; Corbet, B. P.; Giannerini, M.; Feringa, B. L. Org. Lett. 2015, 17, 2262.
[25] Al-Masum, M.; Welch, R. L. Tetrahedron Lett. 2014, 55, 1726.
[26] Patel, P.; Borah, G. Chem. Commun. 2017, 53, 443.
[27] Ruan, J.; Li, X.; Saidi, O.; Xiao, J. J. Am. Chem. Soc. 2008, 130, 2424.
[28] He, K.-H.; Tan, F.-F.; Zhou, C.-Z.; Zhou, G.-J.; Yang, X.-L.; Li, Y. Angew. Chem., Int. Ed. 2017, 56, 3080.
[29] Huckins, J. R.; Rychnovsky, S. D. J. Org. Chem. 2003, 68, 10135.
[30] Scala, A. D.; Garbacia, S.; Hélion, F.; Lannou, M.-I.; Namy, J.-L. Eur. J. Org. Chem. 2002, 2989.
[31] Wu, X.-F.; Neumann, H.; Beller, M. Tetrahedron Lett. 2012, 53, 582.