Issue 20, 2015

Fluorine containing amino acids: synthesis and peptide coupling of amino acids containing the all-cis tetrafluorocyclohexyl motif

Abstract

A synthesis of two (S)-phenylalanine derivatives is described which have the all-cis, 2,3,5,6-tetrafluorocyclohexyl motif attached to the aromatic ring at the meta and para positions; the para substituted isomer is elaborated into illustrative dipeptides via the free amine and carboxylate respectively demonstrating its utility as a novel amino acid for peptide synthesis and offering a vehicle for incorporation of this unique and facially polarized ring system into bioactive compounds.

Graphical abstract: Fluorine containing amino acids: synthesis and peptide coupling of amino acids containing the all-cis tetrafluorocyclohexyl motif

Supplementary files

Article information

Article type
Communication
Submitted
01 Apr 2015
Accepted
15 Apr 2015
First published
15 Apr 2015

Org. Biomol. Chem., 2015,13, 5621-5624

Author version available

Fluorine containing amino acids: synthesis and peptide coupling of amino acids containing the all-cis tetrafluorocyclohexyl motif

M. S. Ayoup, D. B. Cordes, A. M. Z. Slawin and D. O'Hagan, Org. Biomol. Chem., 2015, 13, 5621 DOI: 10.1039/C5OB00650C

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