Issue 16, 2020

Non-biaryl atropisomerism at the C–B bond in sterically hindered aminoarylboranes

Abstract

Sterically hindered aminoarylboranes featuring atropisomerism about the C–B bond were prepared by addition of organomagnesium species onto readily accessible dialkylamine–borane complexes. Some of these aminoarylboranes, isosteres of vinyl styrene derivatives, were resolved by HPLC on the chiral stationary phase. They are the first examples of a non-biaryl type system which display slow rotation about a C–B bond.

Graphical abstract: Non-biaryl atropisomerism at the C–B bond in sterically hindered aminoarylboranes

Supplementary files

Article information

Article type
Communication
Submitted
26 Feb 2020
Accepted
31 Mar 2020
First published
31 Mar 2020

Org. Biomol. Chem., 2020,18, 3007-3011

Non-biaryl atropisomerism at the C–B bond in sterically hindered aminoarylboranes

M. Birepinte, F. Robert, S. Pinet, L. Chabaud and M. Pucheault, Org. Biomol. Chem., 2020, 18, 3007 DOI: 10.1039/D0OB00421A

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