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Collect. Czech. Chem. Commun. 2007, 72, 1697-1706
https://doi.org/10.1135/cccc20071697

Synthesis of N-[(3-Amino-1,2-dicarba-closo-dodecaboran-1-yl)acetyl] Derivatives of α-Amino Acids

Galina L. Levita,*, Victor P. Krasnova, Dmitriy A. Gruzdeva, Alexander M. Demina, Iliya V. Bazhova, Liliya Sh. Sadretdinovaa, Valentina A. Olshevskayab, Valery N. Kalininb, Chan Seong Cheongc, Oleg N. Chupakhina and Valery N. Charushina

a Postovsky Institute of Organic Synthesis of Russian Academy of Sciences (Ural Division), 620041 Ekaterinburg, Russian Federation
b Laboratory of Fine Organic Synthesis, A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 119991 Moscow, Russian Federation
c Life Sciences Division, Korea Institute of Science and Technology, 130-650 Seoul, Korea

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  • Telegina A. A., Gruzdev D. A., Levit G. L., Krasnov V. P.: Synthesis of a novel planar-chiral nido-carborane amino acid. Russ Chem Bull 2021, 70, 539. <https://doi.org/10.1007/s11172-021-3121-7>
  • Gruzdev Dmitry A., Levit Galina L., Krasnov Victor P., Charushin Valery N.: Carborane-containing amino acids and peptides: Synthesis, properties and applications. Coordination Chemistry Reviews 2021, 433, 213753. <https://doi.org/10.1016/j.ccr.2020.213753>
  • Cheng Ruofei, Zhang Jie, Zhang Huifang, Qiu Zaozao, Xie Zuowei: Ir-catalyzed enantioselective B−H alkenylation for asymmetric synthesis of chiral-at-cage o‑carboranes. Nat Commun 2021, 12. <https://doi.org/10.1038/s41467-021-27441-y>
  • Rodríguez-Rey José Luis, Esteban-Gómez David, Platas-Iglesias Carlos, Sousa-Pedrares Antonio: Electronic versus steric control in palladium complexes of carboranyl phosphine-iminophosphorane ligands. Dalton Trans. 2019, 48, 486. <https://doi.org/10.1039/C8DT04006K>
  • Gruzdev Dmitry A., Ustinova Veronika O., Chulakov Evgeny N., Ol'shevskaya Valentina A., Slepukhin Pavel A., Levit Galina L., Krasnov Victor P., Charushin Valery N.: Preparation of enantiomerically pure derivatives of (3-amino-1,2-dicarba-closo-dodecaboran-1-yl)acetic acid. Journal of Organometallic Chemistry 2018, 876, 50. <https://doi.org/10.1016/j.jorganchem.2018.08.018>
  • Cheng Ruofei, Li Bowen, Wu Jie, Zhang Jie, Qiu Zaozao, Tang Wenjun, You Shu-Li, Tang Yong, Xie Zuowei: Enantioselective Synthesis of Chiral-at-Cage o-Carboranes via Pd-Catalyzed Asymmetric B–H Substitution. J. Am. Chem. Soc. 2018, 140, 4508. <https://doi.org/10.1021/jacs.8b01754>
  • Gruzdev Dmitry A., Nuraeva Alla S., Slepukhin Pavel A., Levit Galina L., Zelenovskiy Pavel S., Shur Vladimir Ya., Krasnov Victor P.: Piezoactive amino acid derivatives containing fragments of planar-chiral ortho-carboranes. J. Mater. Chem. C 2018, 6, 8638. <https://doi.org/10.1039/C8TC02266F>
  • Gruzdev D. A., Levit G. L., Olshevskaya V. A., Krasnov V. P.: Synthesis of ortho-carboranyl derivatives of (S)-asparagine and (S)-glutamine. Russ J Org Chem 2017, 53, 769. <https://doi.org/10.1134/S1070428017050190>
  • Nuraeva A. S., Vasileva D. S., Vasilev S. G., Zelenovskiy P. S., Gruzdev D. A., Krasnov V. P., Olshevskaya V. A., Kalinin V. N., Shur V. Ya.: Piezoelectric and ferroelectric properties of organic single crystals and films derived from chiral 2-methoxy and 2-amino acids. Ferroelectrics 2016, 496, 1. <https://doi.org/10.1080/00150193.2016.1155037>
  • Scholz Matthias, Hey-Hawkins Evamarie: Carbaboranes as Pharmacophores: Properties, Synthesis, and Application Strategies. Chem. Rev. 2011, 111, 7035. <https://doi.org/10.1021/cr200038x>
  • Gruzdev D. A., Levit G. L., Bazhov I. V., Demin A. M., Sadretdinova L. Sh., Ol’shevskaya V. A., Kalinin V. N., Krasnov V. P., Chupakhin O. N.: Synthesis of novel carboranyl derivatives of α-amino acids. Russ Chem Bull 2010, 59, 110. <https://doi.org/10.1007/s11172-010-0052-0>