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Cyclic β-Peptoids

Authors :
Claude Taillefumier
Sophie Faure
Claude Didierjean
Vincent Théry
Olivier Roy
Synthèse et étude de systèmes à intêret biologique (SEESIB)
Université Blaise Pascal - Clermont-Ferrand 2 (UBP)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)
Cristallographie, Résonance Magnétique et Modélisations (CRM2)
Université de Lorraine (UL)-Centre National de la Recherche Scientifique (CNRS)
Université Blaise Pascal - Clermont-Ferrand 2 (UBP)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)
Source :
Organic Letters, Organic Letters, 2008, 10, pp.921-924, Organic Letters, American Chemical Society, 2008, 10, pp.921-924, HAL
Publication Year :
2008
Publisher :
American Chemical Society (ACS), 2008.

Abstract

The first synthesis of functionalized beta-peptoid macrocycles is reported. X-ray crystallographic structure of tetramer 9 reveals a C2-symmetrical derivative with unexpected all-cis-amide bonds and spatial disposition of the appendages toward the two opposite faces of the ring. Quantum calculations suggest that 9 is locked in this layout. These macrocycles constitute novel promising templates for multimeric ligation of biologically active ligands. The concept was exemplified by chemical decoration of tetramer 9 via "click" reactions.

Details

ISSN :
15237052 and 15237060
Volume :
10
Database :
OpenAIRE
Journal :
Organic Letters
Accession number :
edsair.doi.dedup.....e899f6386ac0a6a5ace46cabf2af7126