Folding and self-assembly of aromatic and aliphatic urea oligomers: Towards connecting structure and function

被引:109
作者
Fischer, Lucile [2 ]
Guichard, Gilles [1 ]
机构
[1] Univ Bordeaux, CNRS, UMR 5248, Inst Europeen Chim & Biol,CBMN, F-33607 Pessac, France
[2] Univ Calif San Diego, La Jolla, CA 92093 USA
关键词
SOLID-PHASE SYNTHESIS; DE-NOVO DESIGN; VACUUM-ULTRAVIOLET-SPECTRA; BAYLIS-HILLMAN REACTION; HOST-DEFENSE PEPTIDES; ASYMMETRIC CATALYSIS; CRYSTAL-STRUCTURES; BETA-PEPTIDES; SUPRAMOLECULAR POLYMERS; ANTIMICROBIAL PEPTIDES;
D O I
10.1039/c001090a
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Folding and self-assembly of biomacromolecules has inspired the development of discrete, non-natural oligomers that fold and/or self-assemble in a controlled manner. Though aromatic and aliphatic oligoamides remain unmatched for structural diversity and synthetic versatility, oligomers based on amide bond surrogates, such as urea backbones, also demonstrated a propensity for folding and self-assembly. In this Perspective, we review the advances in the design of oligomeric aromatic and aliphatic urea sequences (essentially N,N'-linked) that fold and/or self-assemble. Whenever applicable, the relationship between structure and function will be highlighted.
引用
收藏
页码:3101 / 3117
页数:17
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