___

• [1] Fernandes, G. F. S., Denny, W. A., & Dos Santos, J. L. (2019). Boron in drug design: Recent advances in the development of new therapeutic agents. Eur J Med Chem, 179, 791-804.
• [2] Frankland E., D. B. (1860). Justus Liebigs Annalen der Chem, 115(3), 319-322.
• [3] Hall, D. G. (2011). Structure, Properties, and Preparation of Boronic Acid Derivatives Overview of Their Reactions and Applications. Boronic Acids: Preparation and Applications in Organic Synthesis, Medicine and Materials, Second Edition, 1-133.
• [4] Kilic, A., Balci, T. E., Arslan, N., Aydemir, M., Durap, F., Okumuş, V., & Tekin, R. (2020). Synthesis of cis 1,2‐diol‐type chiral ligands and their dioxaborinane derivatives: Application for the asymmetric transfer hydrogenation of various ketones and biological evaluation. Applied Organometallic Chemistry, 34(10), e5835.
• [5] Nishiyabu, R., Kubo, Y., James, T. D., & Fossey, J. S. (2011). Boronic acid building blocks: tools for self assembly. Chem Commun, 47(4), 1124-1150.
• [6] Heleg-Shabtai, V., Aizen, R., Orbach, R., Aleman-Garcia, M. A., & Willner, I. (2015). Gossypol-cross-linked boronic acid-modified hydrogels: a functional matrix for the controlled release of an anticancer drug. Langmuir, 31(7), 2237-2242.
• [7] Sek, J. P., Kaczmarczyk, S., Gunka, K., Kowalczyk, A., Borys, K. M., Kasprzak, A., & Nowicka, A. M. (2021). Boronate-appended polymers with diol-functionalized ferrocene: an effective and selective method for voltammetric glucose sensing. Dalton Trans, 50(3), 880-889.
• [8] Tanaka, K., Chujo, Y., Ito, S., & Gon, M. (2021). Recent developments in stimuli-responsive luminescent polymers composed of boron compounds. Polym. Chem., 12(44), 6372-6380.
• [9] Cheng, F., & Jäkle, F. (2011). Boron-containing polymers as versatile building blocks for functional nanostructured materials. Polymer Chemistry, 2(10), 2122-2132.
• [10] Cambre, J. N., & Sumerlin, B. S. (2011). Biomedical applications of boronic acid polymers. Polymer, 52(21), 4631-4643.
• [11] Jakle, F. (2010). Advances in the Synthesis of Organoborane Polymers for Optical, Electronic, and Sensory Applications. Chem. Rev., 110, 3985-4022.
• [12] Ma, R., & Shi, L. (2014). Phenylboronic acid-based glucose-responsive polymeric nanoparticles: synthesis and applications in drug delivery. Polym. Chem., 5(5), 1503-1518.
• [13] Yan, Y., Zhou, L., Sun, Z., Song, D., & Cheng, Y. (2022). Targeted and intracellular delivery of protein therapeutics by a boronated polymer for the treatment of bone tumors. Bioact Mater, 7, 333-340.
• [14] Kilic, A., Sobay, B., Aytar, E., & Söylemez, R. (2020). Synthesis and effective catalytic performance in cycloaddition reactions with CO2 of boronate esters versus N-heterocyclic carbene (NHC)-stabilized boronate esters. Sustainable Energy & Fuels, 4(11), 5682-5696.
• [15] Jiménez, C. C., Farfán, N., Romero-Avila, M., Rodríguez, M., Aparicio-Ixta, L., Ramos-Ortiz, G., Maldonado, J. L., Santillan, R., Magana-Vergara, N.E., & Ochoa, M. E. (2014). Synthesis and chemical-optical characterization of novel two-photon fluorescent borinates derived from Schiff bases. Journal of Organometallic Chemistry, 755, 33-40.
• [16] Kilic, A., Savci, A., Alan, Y., & Birsen, H. (2021). Synthesis and spectroscopic properties of 4,4′-bipyridine linker bioactive macrocycle boronate esters: photophysical properties and antimicrobial with antioxidant studies. Journal of Organometallic Chemistry, 941(7), 121807.
• [17] Kilic, A., Patlak, B., Aydemir, M., & Durap, F. (2022). Preparation of catechol boronate esters enabled by N→B dative bond as efficient, stable, and green catalysts for the transfer hydrogenation of various ketones. Inorganica Chimica Acta, 534, 120812.
• [18] Schmidt, M. P., Siciliano, S. D., & Peak, D. (2021). The role of monodentate tetrahedral borate complexes in boric acid binding to a soil organic matter analogue. Chemosphere, 276, 130150.
• [19] Yuan, P., Cai, C., Tang, J., Qin, Y., Jin, M., Fu, Y., Li, Z., & Ma X. (2016). Anion acceptors diox- aborinane contained in solid state polymer electrolyte: preparation, character- ization, and DFT calculations, Adv. Funct. Mater, 26, 5930-5939.
• [20] Cheng, J., Wei, K., Ma, X., Zhou, X., & Xiang, H. (2013). Synthesis and Photophysical Properties of Colorful Salen-Type Schiff Bases. J. Phys. Chem. C, 117(32), 16552-16563.
• [21] Şen, P. (2019). Synthesis of a new boron complex with imine ligand: Synthesis, characterization and fluorescent properties. BORON, 4(1), 46-52.
• [22] SahooSaikat, S., Maiti, S., Poddar, P., & Dhara, D. (2020). Cationic cross-linked polymers containing labile disulfide and boronic ester linkages for effective triple responsive DNA release. Colloids and Surfaces B: Biointerfaces, 191, 110988.