Issue 47, 2022

Stable d-xylose ditriflate in divergent syntheses of dihydroxy prolines, pyrrolidines, tetrahydrofuran-2-carboxylic acids, and cyclic β-amino acids

Abstract

Double nucleophilic displacement of D-xylo-ditriflate by amines, water and alkyl cyanoacetates, respectively, gave a series of bicyclic divergent intermediates for the synthesis of a wide range of highly functionalized targets, including hydroxylated prolines, pyrrolidines, furanoic acids, and cyclopentanes.

Graphical abstract: Stable d-xylose ditriflate in divergent syntheses of dihydroxy prolines, pyrrolidines, tetrahydrofuran-2-carboxylic acids, and cyclic β-amino acids

Supplementary files

Article information

Article type
Paper
Submitted
13 Jul 2022
Accepted
26 Oct 2022
First published
26 Oct 2022

Org. Biomol. Chem., 2022,20, 9447-9459

Stable D-xylose ditriflate in divergent syntheses of dihydroxy prolines, pyrrolidines, tetrahydrofuran-2-carboxylic acids, and cyclic β-amino acids

R. Balo, A. G. Fernández, A. Chopdat, S. E. Ayadi, A. Kato, R. J. Estévez, G. W. J. Fleet and J. C. Estévez, Org. Biomol. Chem., 2022, 20, 9447 DOI: 10.1039/D2OB01255C

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