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

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Abstract

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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Drouin, M., & Paquin, J. F. (2017). Recent progress in the Racemic and enantioselective synthesis of monofluoroalkene-based dipeptide isosteres. Beilstein Journal of Organic Chemistry, 13, 2637–2658. https://doi.org/10.3762/bjoc.13.262

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