4.1 Article

Synthesis of Substituted Derivatives of closo-Decaborate Anion with a Peptide Bond: The Way towards Designing Biologically Active Boron-Containing Compounds

Journal

RUSSIAN JOURNAL OF INORGANIC CHEMISTRY
Volume 64, Issue 12, Pages 1499-1506

Publisher

MAIK NAUKA/INTERPERIODICA/SPRINGER
DOI: 10.1134/S003602361912012X

Keywords

closo-decaborate anion; nitrile derivatives; nucleophilic addition; dipeptides

Funding

  1. Russian Foundation for Basic Research [19-03-00218_a]
  2. Council of Russian Federation Presidential Grants [MK-2403.2019.3, NSh-2845.2018.3]

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A novel scheme of multi-step synthesis for N-borylated dipeptide R-GlyPheOEt is proposed, which is based on the nucleophilic addition of amino acid derivatives to the [2-B10H9NCCH3](-) anion. The products obtained at each step were studied by NMR, IR spectroscopy, and ESI mass spectrometry. The single-crystal structure of (NBu4)[2-B10H9NH=C((NH2CH2COOC4H9)-C-t)CH3] was identified by XRD.

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