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.
Supplementary materials
Title
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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