• Vera V. Voinova
  • Nikita A. Selivanov
  • Ivan V. Plyushchenko
  • Mikhail F. Vokuev
  • Alexander Yu Bykov
  • Ilya N. Klyukin
  • Alexander S. Novikov
  • Andrey P. Zhdanov
  • Mikhail S. Grigoriev
  • Igor A. Rodin
  • Konstantin Yu Zhizhin
  • Nikolay T. Kuznetsov

The novel members of the 1,2-diboraoxazoles family have been obtained. In the present work, we have carried out the intramolecular ring-closure reaction of borylated iminols of general type [B10H9N=C(OH)R]- (R = Me, Et, nPr, iPr, tBu, Ph, 4-Cl-Ph). This process is conducted in mild conditions with 83-87% yields. The solid-state structures of two salts of 1,2-diboraoxazoles were additionally investigated by X-ray crystallography. In addition, the phenomena of bonding interactions in the 1,2-diboraoxazole cycles have been theoretically studied by the Quantum Theory of Atoms in Molecules analysis. Several local and integral topological properties of the electron density involved in these interactions have been computed.

Original languageEnglish
Article number248
Number of pages14
JournalMolecules (Basel, Switzerland)
Volume26
Issue number1
DOIs
StatePublished - 5 Jan 2021

    Research areas

  • closo-decaborate, diboraoxazole, iminol, intramolecular ring-closure reaction, QTAIM analysis, ASTATINATION, REAGENTS, MECHANISM, COMPLEXES, CARBORANE, CLUSTER, B-H, DERIVATIVES

    Scopus subject areas

  • Drug Discovery
  • Analytical Chemistry
  • Chemistry (miscellaneous)
  • Molecular Medicine
  • Physical and Theoretical Chemistry
  • Pharmaceutical Science
  • Organic Chemistry

ID: 73921877