S. Liu, S. Jin, H. Wang et al.
Tetrahedron Letters 68 (2021) 152950
Adv. 2014, 4, 54409-54415. (g) Badsara, S. S.; Liu, Y.-C.; Hsieh, P.-A.; Zeng, J.-
W.; Lu, S.-Y.; Liu, Y.-W.; Lee, C.-F. Chem. Commun. 2014, 50, 11374-11377.
9] The selected examples for nickel-catalyzed C- or N-dehydrogenation: (a)
Irrgang, T.; Kempe, R. Chem. Rev. 2019, 119, 2524-2549. (b) Bera, S.; Bera, A.;
Banerjee, D. Org. Lett. 2020, 22, 6458-6463. (c) Das, J.; Vellakkaran, M.;
Banerjee, D. Chem. Commun. 2019, 55, 7530-7533. (d) Vellakkaran, M.; Das, J.;
Bera, S.; Banerjee, D. Chem. Commun. 2018, 54, 12369-12372.
Appendix A. Supplementary data
[
[
10] The selected examples for Yamaguchi’s works: Review: M. Arisawa, M.
Yamaguchi, Pure Appl. Chem. 80 (2008) 993–1003. References: Arisawa, M.;
Fujimoto, K.; Morinaka, S.; Yamaguchi, M. J. Am. Chem. Soc. 2005, 127, 12226-
References
[
1] The selected examples for thioether in the area of pharmaceutical: (a) R.K.
Cady, P.J. McAllister, E.L. Spierings, H.J. Messina, J. Carothers, P.G. Djupesland,
R.A. Mahmoud, Headache (2015) 88–100; (b) E.A. Ilardi, E. Vitaku, J.T.
[
3] The selected review for thioether in the area of polymeric material: Shen, Y.;
5] The selected examples for the synthesis of thioethers: (a) Lou, J.; Wang, Q.; Wu,
P.; Wang, H.; Zhou, Y.-G.; Yu, Z. Chem. Soc. Rev. 2020, 49, 4307-4359. (b) St
John-Campbella, S.; Bull, J. A. Adv. Synth. Catal. 2019, 361, 3662-3682. (c) Shen,
C.; Zhang, P.; Sun, Q.; Bai, S.; Hor, T. S. A.; Liu, X. Chem. Soc. Rev. 2015, 44, 291-
[
[
[
[14] The examples for our previous works: (a) Qin, G.; Chen, X.; Yang, L.; Huang, H.
ACS Catal. 2015, 5, 2882-2885. (b) Xie, P.; Xia, C.; Huang, H. Org. Lett. 2013, 15,
3370-3373. (c) Xie, P.; Xie, Y.; Qian, B.; Zhou, H.; Xia, C.; Huang, H. J. Am. Chem.
Soc. 2012, 134, 9902-9905.
3
14. (d) Chauhan, P.; Mahajan, S.; Enders, D. Chem. Rev. 2014, 114, 8807-8864.
(
e) Beletskaya, I. P.; Ananikov, V. P. Chem. Rev. 2011, 111, 1596-1636.
[15] The selected examples for hydrogen atom abstraction process: a) Tanwar, L.;
Börgel, J.; Ritter, T. J. Am. Chem. Soc. 2019, 141, 17983-17988. (b) Marko, J. A.;
Durgham, A.; Bretz, S. L.; Liu, W. Chem. Commun. 2019, 55, 937-940. (c) Lewis,
E. S.; Ogino, K. J. Am. Chem. Soc. 1976, 98, 2264-2268. (d) Totherow, W. D.;
Gleicher, G. J. J. Am. Chem. Soc. 1969, 91, 7150-7154.
[
[
6] The selected examples for transition-metal catalyzed sulfenylations of sp3 C-H
bond: (a) Huang, L.-S.; Han, D.-Y.; Xu, D.-Z. Adv. Synth. Catal. 2019, 361, 4016-
4
021. (b) Liu, C.; Szostak, M. Chem. Commun. 2018, 54, 2130-2133. (b) Yan, S.-
Y.; Liu, Y.-J.; Liu, Y.-H.; Zhang, Z.-Z.; Shi, B.-F. Chem. Commun. 2015, 51, 7341-
344. (c) Ye, X.; Petersen, J. L.; Shi, X. Chem. Commun. 2015, 51, 7863-7866. (d)
7
[16] The selected examples for Ni-catalyzed radical reactions: (a) Yuan, M.; Song,
Z.; Badir, S. O.; Molander, G. A.; Gutierrez, O. J. Am. Chem. Soc. 2020, 142,
7225-7234. (b) Wei, X.; Shu, W.; García-Domínguez, A.; Merino, E.; Nevado, C.
J. Am. Chem. Soc. 2020, 142, 13515-13522. (c) Sun, R.; Qin, Y.; Nocera, D. G.
Angew. Chem. Int. Ed. 2020, 59, 9527-9533. (d) Tang, Y.-Q.; Yang, J.-C.; Wang,
L.; Fan, M.; Guo, L.-N. Org. Lett. 2019, 21, 5178-5182. (e) Stadler, S. M.;
Göttker-Schnetmann, I.; Mecking, S. ACS Catal. 2019, 9, 2760-2767. (f) Liu, S.;
Qi, X.; Bai, R.; Lan, Y. J. Org. Chem. 2019, 84, 3321-3327. (g) Komeyama, K.;
Michiyuki, T.; Osaka, I. ACS Catal. 2019, 9, 9285-9291. (h) Zheng, S. Gutiérrez-
Bonet, Á.; Molander, G. A. Chem, 2019, 5, 339-352. (i) Angelini, L.; Davies, J.;
Simonetti, M.; Sanz, M. L.; Sheikh, N. S.; Leonori, D. Angew. Chem. Int. Ed. 2019,
58, 5003-5007. (j) Soni, V.; Khake, S. M.; Punji, B. ACS Catal. 2017, 7, 4202-
4208. (k) Qin, T.; Malins, L. R.; Edwards, J. T.; Merchant, R. R.; Novak, A. J. E.;
Zhong, J. Z.; Mills, R. B.; Yan, M.; Yuan, C.; Eastgate, M. D.; Baran, P. S. Angew.
Chem. Int. Ed. 2017, 56, 260-265. (l) Shaw, M. H.; Shurtleff, V. W.; Terrett, J. A.
Science, 2016, 352, 1304-1308. (m) Noble, A.; McCarver, S. J.; MacMillan, D. W.
C. J. Am. Chem. Soc. 2015, 137, 624-627. (n) Aihara, Y.; Tobisu, M.; Fukumoto,
Y.; Chatani, N. J. Am. Chem. Soc. 2014, 136, 15509-15512.
Lin, C.; Yao, J.; Wang, B.; Liu, Z.; Zhang, Y. Org. Lett. 2015, 17, 1340-1343. (e)
Wang, X.; Qiu, R.; Yan, C.; Reddy, V. P.; Zhu, L.; Xu, X.; Yin, S.-F. Org. Lett. 2015,
1
7] The selected reviews for transition-metal catalyzed C(sp3)-H bond
functionalization: (a) Qin, Y.; Zhu, L.; Luo, S. Chem. Rev. 2017, 117, 9433-
9
1
2
7
5
7, 1970-1973.
520. (b) He, J.; Wasa, M.; Chan, K. S. L.; Shao, Q.; Yu, J.-Q. Chem. Rev. 2017,
17, 8754-8786. (c) He, G.; Wang, B.; Nack, W. A.; Chen, G. Acc. Chem. Res.
016, 49, 635-645. (d) Miao, J.; Ge, H. Eur. J. Org. Chem. 2015, 2015, 7859-
868. (e) Xie, J.; Pan, C.; Abdukadera, A.; Zhu, C. Chem. Soc. Rev. 2014, 43,
245-5256. (f) Dastbaravardeh, N.; Christakakou, M.; Haider, M.; Schnürch, M.
Synthesis 2014, 46, 1421-1439. (g) Baudoin, O. Chem. Soc. Rev. 2011, 40, 4902-
911. (h) Jazzar, R.; Hitce, J.; Renaudat, A.; Sofack-Kreutzer, J.; Baudoin, O.
4
Chem. -Eur. J. 2010, 16, 2654-2672.
[
8] The selected examples for previous oxidative dehydrogenative coupling
reaction of alkane with sulfur reagent: (a) Pramanik, M.; Choudhuri, K.; Mal,
P. Org. Biomol. Chem. 2020, 18, 8771-8792. (b) Zhao, F.; Tan, Q.; Wang, D.;
Chen, J.; Deng, G.-J. Adv. Synth. Catal. 2019, 361, 4075-4081. (c) Du, B.; Jin, B.;
Sun, P. Org. Lett. 2014, 16, 3032-3035. (d) Zhao, J.; Fang, H.; Han, J.; Pan, Y.; Li,
G. Adv. Synth. Catal. 2014, 356, 2719-2724. (e) Yuan, J.; Ma, X.; Yi, H.; Liu, C.;
Lei, A. Chem. Commun. 2014, 50, 14386-14389. (f) Feng, J.; Lu, G.-P.; Cai, C. RSC
[17] The selected examples for the ligand exchange of M(OAc)2 with thiol: (a) Hui
Xi, Enlu Ma, Zhiping Li, Tetrahedron 72 (2016) 4111–4116; (b) T. Tamai, A.
Ogawa, J. Org. Chem. 79 (2014) 5028–5035.
5