| Literature DB >> 33466558 |
Vera V Voinova1, Nikita A Selivanov1, Ivan V Plyushchenko2, Mikhail F Vokuev2, Alexander Yu Bykov1, Ilya N Klyukin1, Alexander S Novikov3, Andrey P Zhdanov1, Mikhail S Grigoriev4, Igor A Rodin2, Konstantin Yu Zhizhin1, Nikolay T Kuznetsov1.
Abstract
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.Entities:
Keywords: QTAIM analysis; closo-decaborate; diboraoxazole; iminol; intramolecular ring-closure reaction
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Year: 2021 PMID: 33466558 PMCID: PMC7796516 DOI: 10.3390/molecules26010248
Source DB: PubMed Journal: Molecules ISSN: 1420-3049 Impact factor: 4.411