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Original Articles

ADVANCES AT THE INTERFACE OF POLYHEDRAL BORANE CHEMISTRY AND MEDICINE

Pages 153-163 | Published online: 25 Nov 2010

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Zbigniew J. Leśnikowski. (2016) Recent developments with boron as a platform for novel drug design. Expert Opinion on Drug Discovery 11:6, pages 569-578.
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Articles from other publishers (16)

Katia Messner, Billy Vuong & Geoffrey K. Tranmer. (2022) The Boron Advantage: The Evolution and Diversification of Boron’s Applications in Medicinal Chemistry. Pharmaceuticals 15:3, pages 264.
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Chun-hua Tan, Bao-kai Zhang, Jie Chen, Lin-na Zhang, Xu-guang Huang & Hong-yun Meng. (2019) Study of Hydrolysis Kinetic of New Laser Material [anti-B18H22]. Russian Journal of Inorganic Chemistry 64:11, pages 1359-1364.
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Baokai Zhang, Jie Chen, Linli Xiong, Linna Zhang, Chunhua Tan, Xuguang Huang & Hongyun Meng. (2019) Hydrolysis Kinetic of New Laser Material n- B 18 H 22 . IOP Conference Series: Earth and Environmental Science 242, pages 022040.
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Chen-Hao Lin, Vladimir N. Nesterov & Michael G. Richmond. (2018) Synthesis and redox properties of fac-BrRe(CO)3[1,2-(PPh2)2-closo-1,2-C2B10H10]: The first structurally characterized rhenium carbonyl containing a carboranyl-based diphosphine ligand. Journal of Molecular Structure 1156, pages 397-402.
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Mikhail M. Vinogradov, Yulia V. Nelyubina, Alexander A. Pavlov, Valentin V. Novikov, Nikita V. Shvydkiy & Alexander R. Kudinov. (2017) Polyhedral Rearrangements in the Complexes of Rhodium and Iridium with Isomeric Carborane Anions [7,8-Me 2 -X-SMe 2 -7,8- nido -C 2 B 9 H 8 ] − (X = 9 and 10) . Organometallics 36:4, pages 791-800.
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Yuanbin Zhang, Yuji Sun, Furong Lin, Jiyong Liu & Simon Duttwyler. (2016) Rhodium(III)-Catalyzed Alkenylation-Annulation of closo -Dodecaborate Anions through Double B?H Activation at Room Temperature . Angewandte Chemie International Edition 55:50, pages 15609-15614.
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Yuanbin Zhang, Yuji Sun, Furong Lin, Jiyong Liu & Simon Duttwyler. (2016) Rhodium(III)-Catalyzed Alkenylation-Annulation of closo -Dodecaborate Anions through Double B−H Activation at Room Temperature . Angewandte Chemie 128:50, pages 15838-15843.
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Zbigniew J. Leśnikowski. (2016) Challenges and Opportunities for the Application of Boron Clusters in Drug Design. Journal of Medicinal Chemistry 59:17, pages 7738-7758.
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Muddamarri Hanumantha Rao & Krishnamurthi Muralidharan. (2016) closo-Dodecaborate (B12H12)2− salts with nitrogen based cations and their energetic properties. Polyhedron 115, pages 105-110.
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René Frank, Verena Ahrens, Solveig Boehnke, Sven Hofmann, Martin Kellert, Stefan Saretz, Souvik Pandey, Menyhárt Sárosi, Ágota Bartók, Annette G. Beck-Sickinger & Evamarie Hey-Hawkins. (2015) Carbaboranes – more than just phenyl mimetics. Pure and Applied Chemistry 87:2, pages 163-171.
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Jan U. Kahlert, Aditya Rawal, James M. Hook, Louis M. Rendina & Mohammad Choucair. (2014) Carborane functionalization of the aromatic network in chemically-synthesized graphene. Chemical Communications 50:77, pages 11332.
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Antonio Toppino, Afaf R. Genady, Mohamed E. El-Zaria, James Reeve, Fargol Mostofian, Jeff Kent & John F. Valliant. (2013) High Yielding Preparation of Dicarba- closo -dodecaboranes Using a Silver(I) Mediated Dehydrogenative Alkyne-Insertion Reaction . Inorganic Chemistry 52:15, pages 8743-8749.
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J. Liu, X. Zhang, D.E. Bowen, E.A. Eastwood & N. Bowler. (2013) Plasticization and reinforcement in a boron cage compound polyurethane nanocomposite: A dielectric study. Journal of Non-Crystalline Solids 371-372, pages 6-13.
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Clara Viñas i Teixidor. (2013) The uniqueness of boron as a novel challenging element for drugs in pharmacology, medicine and for smart biomaterials. Future Medicinal Chemistry 5:6, pages 617-619.
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Anika S. Louie, Laura E. Harrington & John F. Valliant. (2012) The preparation and characterization of functionalized carboranes and Re/Tc-metallocarboranes as platforms for developing molecular imaging probes: Structural and cage isomerism studies. Inorganica Chimica Acta 389, pages 159-167.
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René Frank, Solveig Boehnke, Almaz Aliev & Evamarie Hey-Hawkins. (2012) From ortho-carbaborane-9-thiol towards new building blocks. Polyhedron 39:1, pages 9-13.
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