Enantioselective Recognition of a Chiral Quaternary Ammonium Ion by C3 Symmetric Cyclic Hexapeptides

Heinrichs, Guido; Vial, Laurent; Lacour, Jérôme; Kubik, Stefan

doi:10.1039/b302092d

Scientific article

English

Enantioselective Recognition of a Chiral Quaternary Ammonium Ion by C3 Symmetric Cyclic Hexapeptides

ContributorsHeinrichs, Guido; Vial, Laurent; Lacour, Jérôme

; Kubik, Stefan

Published inChemical communications, vol. 38, no. 11, p. 1252-1253

Publication date2003

Abstract

Cyclic hexapeptides containing aromatic amino acid subunits represent the first class of artificial cation hosts with which a significant level of enantioselective recognition of chiral quaternary ammonium ions can be achieved.

Affiliation entities

Faculté des sciences / Section de chimie et biochimie / Département de chimie organique

Citation (ISO format)

HEINRICHS, Guido et al. Enantioselective Recognition of a Chiral Quaternary Ammonium Ion by C3 Symmetric Cyclic Hexapeptides. In: Chemical communications, 2003, vol. 38, n° 11, p. 1252–1253. doi: 10.1039/b302092d

Article

Identifiers

PID : unige:6963
DOI : 10.1039/b302092d

Journal ISSN1359-7345

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Enantioselective Recognition of a Chiral Quaternary Ammonium Ion by C3 Symmetric Cyclic Hexapeptides

Cyclic hexapeptides containing aromatic amino acid subunits represent the first class of artificial cation hosts with which a significant level of enantioselective recognition of chiral quaternary ammonium ions can be achieved.

Technical informations