| [1] |
(a) Koval, I. V. Russ. J. Org. Chem. 2005, 41, 631.
|
|
(b) Uchiro, H.; Kobayashi, S. Tetrahedron Lett. 1999, 40, 3179.
|
|
(c) Testaferri, L.; Tingoli, M.; Tiecco, M. Tetrahedron Lett. 1980, 21, 3099.
|
|
(d) Oae, S.; Togo, H. Tetrahedron Lett. 1982, 23, 4701.
|
|
(e) Hong, S.-M.; Kim, O.; Hwang, S.-H. Materials 2024, 17, 1343.
|
| [2] |
Our recently work on the synthesis of organophosphorus: (a) Zhang, J. Q.; Wang, X.; Wang, T.; Chen, T.; Han, L. B. Green Chem. 2023, 25, 9063.
|
|
(b) Ma, X.; Yan, X. Jing, Y.; Guo, J.; Bian, J.; Yan, R.; Xu, Q.; Han, L. B. Green Chem. 2025, 27, 102.
|
|
(c) Zhang, J.; Hu, W.; Chen, Z.; Wu, N.; Li, C.; Chen, T.; Han, L. B. Org. Lett. 2024, 26, 3386.
|
|
(d) Wang, J.; Xiao, J.; Tang, Z. L.; Lan, D. H.; Han, L. B. J. Org. Chem. 2024, 89, 5109.
|
|
(e) Zhang, J. Q.; Han, L. B. J. Org. Chem. 2024, 89, 2090.
|
| [3] |
Liang, J.; Yang, Y.; Liu, J.; Xu, Q.; Han, L. B. Chin. J. Org. Chem. 2024, 44, 1658 (in Chinese).
|
|
(梁家仪, 杨雅淇, 刘建平, 徐清, 韩立彪, 有机化学, 2024, 44, 1658.)
|
| [4] |
(a) Boström, J.; Brown, D.; Young, R.; Keserü G. M. Nat. Rev. Drug Discovery 2018, 717, 09.
|
|
(b) Li, G.; Lou, H.-X. Med. Res. Rev. 2018, 38, 1255.
|
|
(c) Trivedi, M. V.; Laurence, J. S.; Siahaan, T. Curr. Protein Pept. Sci. 2009, 10, 614.
|
|
(d) Vericat, C.; Vela, M. E.; Benitez, G.; Carro, P.; Salvarezza, R. C. Chem. Soc. Rev. 2010, 39, 1805.
|
|
(e) Feng, M.; Tang, B.; Liang, S. H.; Jiang, X. Curr. Top. Med. Chem. 2016, 16, 1200.
|
| [5] |
Examples of thiophenol conversion to thioether: (a) Eduardo, J.-R.; Hugo, V.; Simon, H.-O.; Rosa, M.; Marcel, S.; David, M.-M. J. Catal. 2023, 426, 247.
|
|
(b) Jati, A.; Dam, S.; Kumar, S.; Kumar, K.; Maji, B. Chem. Sci. 2023, 14, 8624.
|
|
(c) Ji, H.; Cao, H.; Wang, G.; Xing, F.; Szostak, M.; Liu, C. Org. Chem. Front. 2023, 10, 4275.
|
|
(d) Oechsner, R. M.; Lindenmaier, I. H.; Fleischer, I. Org. Lett. 2023, 25, 1655.
|
|
(e) Xu, T.; Zhou, X.; Xiao, X.; Yuan, Y.; Liu, L.; Huang, T.; Li, C.; Tang, Z.; Chen, T. Q. J. Org. Chem. 2022, 87, 8672.
|
| [6] |
Examples of thiophenol conversion to sulfoxides: (a) Liu, Q.; Wang, L.; Yue, H.; Li, J.-S.; Luo, Z.; Wei, W. Green Chem. 2019, 21, 1609.
|
|
(b) Hou, Y.-J.; Li, Y.; Zhao, Z.-W.; Fan, T.-G.; Sun, B.-X.; Wang, X.-N.; Li, Y.-M. Org. Lett. 2023, 25, 517.
|
|
(c) Kim, D. H.; Lee, J.; Lee, A. Org. Lett. 2018, 20, 764.
|
| [7] |
Shyam, P. K.; Kim, Y. K.; Lee, C.; Jang, H.-Y. Adv. Synth. Catal. 2016, 358, 56.
|
| [8] |
Examples of thiophenol conversion to sulfoxides: (a) Laudadio, G.; Bartolomeu, A.; Verwijlen, L. M. H. M.; Cao, Y.; de, Oliveira, K. T.; Noel, T. J. Am. Chem. Soc. 2019, 141, 11832.
|
|
(b) Wang, L.; Cornella, J. Angew. Chem., Int. Ed. 2020, 59, 23510.
|
|
(c) Yamahara, S.; Salem, M. S. H.; Kawai, T.; Watanabe, M.; Sakamoto, Y.; Okada, T.; Kimura, Y.; Takizawa, S.; Kirihara, M. ACS Sustainable Chem. Eng. 2024, 12, 12135.
|
| [9] |
Deryagina, E. N.; Sukhomasova, E. N.; Levanova, E. P.; Papernaya, L. K.; Korchevin, N. A. Russ. J. Org. Chem. 2005, 41, 1624.
|
| [10] |
Dougherty, G.; Hammond, P. D. J. Am. Chem. Soc. 1935, 57, 117.
|
| [11] |
Fan, B.; Zhang, Z.; Liao, Z.; Lv, X.; Tao, M.; Yuan, J.CN 108863867A, 2018.
|
| [12] |
Example of Matal promote reductive cleavage of the S—S: Zhang, M.; Ryckman, D.; Chen, G. E.; MacMillan, J.; Duquette, J. Synthesis 2003, 0112.
|
|
(b) Erlandsson, M.; Hällbrink, M. Int. J. Pept. Res. Ther. 2005, 11, 261.
|
|
(c) Sridhar, M.; Vadivel, S. K.; Bhalerao, U. T. Synth. Commun. 1997, 27, 1347.
|
| [13] |
Selected example of reductive cleavage of the S—S with hydrides: (a) Brown, H. C.; Nazer, B.; Cha, J. S. Synthesis 1984, 6, 498.
|
|
(b) Yoon, N. M.; Gyoung, Y. S. J. Org. Chem. 1985, 50, 2443.
|
|
(c) Ookawa, A.; Yokoyama, S.; Soai, K. Synth. Commun. 1986, 16, 819.
|
|
(d) Kolmakov, K. A.; Kresge, A. J. Can. J. Chem. 2008, 86, 119.
|
|
(e) Kong, F.; Zhou, X. Synth. Commun. 1989, 19, 3143.
|
| [14] |
Maiti, S. N.; Spevak, P.; Singh, M.; Micetich, R. G.; Reddy, A. V. N. Synth. Commun. 1988, 18, 575.
|
| [15] |
(a) Overman, L. E.; Matzinger, D.; O’Connor, E. M.; Overman, J. D. J. Am. Chem. Soc. 1974, 96, 6081.
|
|
(b) Overman, L. E.; Petty, S. T. J. Org. Chem. 1975, 40, 2779.
|
| [16] |
Bai, L.; Jiang, X. CCS Chem. 2025, 7, 1889.
|
| [17] |
(a) Calais, C.; Lacroix, M.; Geantet, C.; Breysse, M. J. Catal. 1993, 144, 160.
|
|
(b) McLaughlin, L.; Novakova, E.; Burchand, R.; Hardacre, C. Appl. Catal., A 2008, 340, 162.
|
|
(c) Novakova, E.; McLaughlin, L.; Burch, R.; Crawford, P.; Griffin, K.; Hardacre, C.; Hu, P.; Rooney, D. J. Catal. 2007, 249, 93.
|
| [18] |
Arisawa, M.; Sugata, C.; Yamaguchi, M. Tetrahedron Lett. 2005, 46, 6097.
|
| [19] |
(a) Arisawa, M.; Yamaguchi, M. Molecules 2020, 25, 3595.
|
|
(b) Arisawa, M.; Suwa, A.; Fujimoto, K.; Yamaguchi, M. Adv. Synth. Catal. 2003, 345, 560.
|
| [20] |
(a) Malviya, B. K.; Hansen, E. C.; Kong, C. J.; Imbrogno, J.; Verghese, J.; Guinness, S. M.; Salazar, C. A.; Desrosiers, J. N.; Kappe, C. O.; Cantillo, D. Chem.-Eur. J. 2023, 29, e202302664.
|
|
(b) Kong, F.; Zhou, X. Synth. Commun. 1989, 19, 3143.
|
|
(c) Jiang, Y.; Qin, Y.; Xie, S.; Zhang, X.; Dong, J.; Ma, D. Org. Lett. 2009, 11, 5250.
|
|
(d) Bergman, J.; Pettersson, B.; Hasimbegovic, V.; Svensson, P. J. Org. Chem. 2011, 76, 1546.
|
| [21] |
Chen, X.; Zhou, S.; Qian, C. J. Sulfur Chem. 2012, 33, 179.
|
| [22] |
(a) Martin, D. P.; Cohen, S. M. Chem. Commun. 2012, 48, 5259.
|
|
(b) Katz, L.; Karger, L. S.; Schroeder, W.; Cohen, M. S. J. Org. Chem. 1953, 18, 1380.
|
| [23] |
Liu, Y.; Kim, J.; Seo, H.; Park, S.; Chae, J. Adv. Synth. Catal. 2015, 357, 2205.
|
| [24] |
(a) Chaudhary, S.; Marilyn, D. M.; Garg, P. A ChemistrySelect 2017, 2, 650.
|
|
(b) Jetti, R. K. R.; Boese, R.; Thakur, T. S.; Vangala, V. R.; Desiraju, G. R. Chem. Commun. 2004, 2526.
|
)
