1. Tréguer P, Nelson DM, Bennekom AJV, DeMaster DJ, Leynaert A, Quéguiner B The Silica Balance in the World Ocean, Struyf E, Smis A, Van Damme S, Meire P, Conley DJ The Global Biogeochemical Silicon Cycle (eds) (1995) : A Rees-timate. Science 268, 375
2. (b) Struyf E, Smis A, Van Damme S, Meire P, Conley DJ The Global Biogeochemical Silicon Cycle. Silicon 1, 207 (2009)
3. Schwarz J (2016) Atypical Elements in Drug Design. Springer, Heidelberg
4. (a) Igawa K, Tomooka K Chiral Silicon Molecules, In Organosilicon Chemistry: Novel Approaches and Reactions, Hiyama E, T., Oestreich M, Wiley, Weinheim, Germany, pp. 495–532 (b), Xu L-W, Li L, Lai G-Q, Jiang J-X (2019) The Recent Synthesis and Application of Silicon-Stereogenic Silanes: A Renewed and Significant Challenge in Asymmetric Synthesis. Chem. Soc. Rev. 40, 1777–1790 (2011). (c) Bauer, J. O. & Strohmann, C. Recent Progress in Asymmetric Synthesis and Application of Difunctionalized Silicon-Stereogenic Silanes. Eur. J. Inorg. Chem. 2016, 2868–2881 (2016). (d) Wu, Y. & Wang, P. Silicon-Stereogenic Monohydrosilane: Synthesis and Applications. Angew. Chem. Int. Ed. 61, e202205382 (2022)
5. (a) Sommer LH, Stereochemistry, Mechanism and (b) Kipping, F. S. XXII. Organic Derivatives of Silicon. Part II. The Synthesis of Benzylethylpropylsilicol, its Sulphonation, and the Resolution of the Dl-sulphonic Derivative into its Optically Active Components J. Chem. Soc. 91, 209–240 (1907). (c) Sommer, L. H. & Silicon; an Introduction to the Dynamic Stereochemistry and Reaction Mechanisms of Silicon Centers; McGraw-Hill: New York, Frye CL, Rendler S, Auer G, Oestreich M Kinetic Resolution of Chiral Secondary Alcohols by Dehydrogena-tive Coupling with Recyclable Silicon-stereogenic Silanes., Rendler S, Oestreich M, Butts CP, Lloyd-Jones GC (1965) Optically Active Organosilicon Compounds Having Reactive Groups Bonded to Asymmetric Silicon. Displacement Reactions at Silicon with Pure Retention and Pure Inversion of Configuration. J. Am. Chem. Soc. 81, 4, 1013 (1959). (d) Yamamoto, K., Kawanami, Y. & Miyazawa, M. Synthesis of a Highly Enantiomerically Enriched Silyllithium Compound. J. Chem. Soc. Chem. Commun. 436 (1993). (e) Strohmann, C., Hörnig, J., & Auer, D. Synthesis of a Highly Enantiomerically Enriched Silyllithium Compound. Chem. Commun. 2, 766–767 (2002). (f) Trzoss, M., Shao, J. & Bienz, S. Preparation of a ‘Si-centered’ Chiral Auxiliary by Resolution. Tetrahedron Asymmetry 15, 1501–1505 (2004). (g) Rendler, S., Auer, G., Oestreich, M. Kinetic Resolution of Chiral Secondary Alcohols by Dehydrogena-tive Coupling with Recyclable Silicon-stereogenic Silanes. Angew. Chem. Int. Ed. 44, 7620–7624 (2005). (h) Rendler, S., Auer, G., Keller, M. & Oestreich, M. Preparation of a Privileged Silicon-stereogenic Silane: Classical Versus Kinetic Resolution. Adv. Synth. Catal. 348, 1171–1182 (2006). (i) Rendler, S., Oestreich, M., Butts, C. P., Lloyd-Jones, G. C. Intermolecular Chirality Transfer from Silicon to Carbon: Interrogation of the Two-silicon Cycle for Pd-catalyzed Hydrosilylation by Stereoisotopochemical Crossover. J. Am. Chem. Soc. 129, 502–503 (2007). (j) Igawa, K., Takada, J., Shimono, T. & Tomooka, K. Enantioselective Synthesis of Silanol. J. Am. Chem. Soc. 130, 16132–16133 (2008). (k) Igawa, K., Kokan, N. & Tomooka, K. Symmetric Synthesis of Chiral Silacarboxylic Acids and Their Ester Derivatives. Angew. Chem. Int. Ed. 49, 728–731 (2010)