Boron Heterocycles via Direct Activation of Nitriles & Carbodiimides by alpha-Heteroboronates

13 January 2026, Version 1
This content is an early or alternative research output and has not been peer-reviewed by Cambridge University Press at the time of posting.

Abstract

Boron heterocycles can be formed at ambient temperature through the reaction of alpha-thio or alpha-amino boronates with nitriles or carbodiiimides. The chemistry can be applied to a wide range of unactivated nitriles. A range of amino acid and peptide analogues containing novel boron heterocycles were generated using these reactions.

Keywords

Boron
Nitriles
Heterocycles
Frustrated Lewis Pairs
Sulfur
Nitrogen

Supplementary materials

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Description
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Supporting Information
Description
Experimental procedures and characterisation data for all compounds, and 1H/13C/11B/19F NMR spectra for novel compounds.
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