Beilstein Journal of Organic Chemistry (Dec 2017)

Recent progress in the racemic and enantioselective synthesis of monofluoroalkene-based dipeptide isosteres

  • Myriam Drouin,
  • Jean-François Paquin

DOI
https://doi.org/10.3762/bjoc.13.262
Journal volume & issue
Vol. 13, no. 1
pp. 2637 – 2658

Abstract

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Monofluoroalkenes are fluorinated motifs that can be used to replace amide bonds. In order to be incorporated into peptides, it is normally necessary to first synthesize a dipeptide where the amide bond has been replaced with a monofluoroalkene. In that context, this review will present the racemic and enantioselective synthesis of monofluoroalkene-based dipeptide isosteres described since 2007. Some applications of those compounds will also be presented.

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