Recent Applications of Hexamethyldisilathiane (TMS2S) in Organic Synthesis

2 For others methods for the preparation of TMS₂S, see: Curphey TJ. Phosphorus, Sulfur, Silicon Relat. Elem. 2001; 173: 123
3 Sigma-Aldrich (accessed March 16, 2023): https://www.sigmaaldrich.com/FR/en/product/aldrich/283134

For selected reviews, see:

4a Matulenko MA, Degl’Innocenti A, Capperucci A. Bis(trimethylsilyl) sulfide . In Encyclopedia of Reagents for Organic Synthesis . Paquette L. Wiley; New York: 2007
4b Degl’Innocenti A, Capperucci A, Castagnoli G, Malesci I. Synlett 2005; 1965
4c Degl’Innocenti A, Capperucci A, Nocentini T, Castagnoli G, Malesci I, Cerreti A. Phosphorus, Sulfur, Silicon Relat. Elem. 2005; 180: 1247

For recent examples, see:

5a Rojas-León I, Christmann J, Schwan S, Ziese F, Sanna S, Mollenhauer D, Rosemann NW, Dehnen S. Adv. Mater. 2022; 34: 2203351
5b Liu LJ, Zhang JW, Asas M, Whang Z.-Y, Zhang S.-Q, Mak TC. W. Chem. Commun. 2021; 57: 5586

See for examples:

6a Sato Y, Nishimura M, Kawaguchi S, Nomoto A, Ogawa A. Chem. Eur. J. 2019; 25: 6797
6b Graham CM. E, Pritchard TE, Boyle PD, Valjus J, Tuononen HM, Ragogna PJ. Angew. Chem. Int. Ed. 2017; 56: 6236
6c Graham CM. E, Macdonald CL. B, Boyle PD, Wisner JA, Ragogna PJ. Chem. Eur. J. 2018; 24: 743

For recent examples, see:

9a Jayaraman J, Ganapathy AS, Thanikachalam V, Palanivel J, Sekar P. J. Phys. Org. Chem. 2018; 31: e3796
9b Kong R, Xiao Z, Xie F, Jiang J, Ding L. New J. Chem. 2017; 41: 2895
9c Kothur RR, Patel BA, Cragg PJ. Chem. Commun. 2017; 53: 9078
9d Wójcik MM, Wróbel J, Jańczuk ZZ, Mieczkowski J, Górecka E, Choi J, Cho M, Pociecha D. Chem. Eur. J. 2017; 23: 8912
9e Rahman ML, Biswas TK, Sarkar SM, Yusoff MM, Yuvaraj AR, Kumar S. J. Colloid Interface Sci. 2016; 478: 384
9f Sun J, Li W, Xiao L, Yu G, Shi J. RSC Adv. 2016; 6: 62200
9g Olshansky JH, Ding TX, Lee YV, Leone SR, Alivisatos AP. J. Am. Chem. Soc. 2015; 137: 15567
9h Liu Y, Najafabadi BK, Fard MA, Corrigan JF. Angew. Chem. Int. Ed. 2015; 54: 4832

10 Kizling M, Dzwonek M, Nowak A, Tymecki L, Stolarczyk K, Więckowska A, Bilewicz B. Nanomaterials 2020; 10: 1434

See also:

12 Ogiwara Y, Takano K, Horikawa S, Sakai N. Molecules 2018; 23: 1339
13 Nie Z, Chiou M.-F, Cui J, Qu Y, Zhu X, Jian W, Xiong H, Li Y, Bao H. Angew. Chem. Int. Ed. 2022; 61: e202202077
14 Sakai N, Horikawa S, Ogiwara Y. Synthesis 2018; 50: 565
15 Degl’Innocenti A, Capperucci A, Cerreti A, Pollicino S, Scapecchi S, Malesci I, Castagnoli G. Synlett 2005; 3063

16a Tanini D, Borgogni C, Capperucci A. New J. Chem. 2019; 43: 6388
16b Tanini D, Barchielli G, Benelli F, Degl’Innocenti A, Capperucci A. Phosphorus, Sulfur, Silicon Relat. Elem. 2015; 190: 1265

17 For a review on ring opening of 1,6-anhydrosugars, see: Hazelard D, Compain P. Eur. J. Org. Chem. 2021; 3501
18 Zhu X, Dere RT, Jiang J, Zhang L, Wang X. J. Org. Chem. 2011; 76: 10187
19 Céspedes DávilaM. F, Schneider JP, Godard A, Hazelard D, Compain P. Molecules 2018; 23: 914
20 Tardieu D, Céspedes DávilaM. F, Hazelard D, Compain P. Synthesis 2018; 50: 3927
21 Ogiwara Y, Maeda H, Sakai N. Synlett 2018; 19: 655
22 Sakai N, Maeda H, Ogiwara Y. Synthesis 2019; 51: 2323
23 Nakajima T, Takeuchi R, Oomori K, Ishida K, Ogiwara Y, Sakai N. Synthesis 2023; 55: 779
24 Tanini D, Angeli A, Capperucci A. Phosphorus, Sulfur, Silicon Relat. Elem. 2016; 191: 156
25 Tanini D, Trapani F, Capperucci A. J. Sulfur Chem. 2020; 41: 635
26 Nakajima T, Takano K, Maeda H, Ogiwara Y, Sakai N. Chem. Asian J. 2021; 16: 4103