Busnel Olivier, Bi Lanrong, Dali Hayet, Cheguillaume Arnaud, Chevance Soizic, Bondon Arnaud, Muller Sylviane, Baudy-Floc'h Michèle
Groupe Ciblage et Auto-Assemblages Fonctionnels, UMR CNRS 6510, Institut de Chimie, Université de Rennes I, Av. du Général Leclerc, F-35042 Rennes Cédex, France.
J Org Chem. 2005 Dec 23;70(26):10701-8. doi: 10.1021/jo051585o.
[structure: see text] A solid-phase fluorenylmethyloxycarbonyl (Fmoc)-based synthesis strategy is described for "mixed" aza-beta3-peptides as well as a convenient general approach for their required building blocks, the aza-beta3-amino acid residues (aza-beta3-aa). These monomers allow the synthesis of relatively large quantities of pure mixed aza-beta3-peptides. The required Fmoc-substituted aza-beta3-amino acids are accessible by convenient synthesis, and a number of monomers including those containing side chains with functional groups have been synthesized. The method was applied toward the solid-phase synthesis of aza-beta3-peptide mimetics of a biologically active histone H4 sequence.
[结构:见文本] 描述了一种基于固相芴甲氧羰基(Fmoc)的合成策略,用于合成“混合”氮杂-β3-肽,以及一种制备其所需构建块——氮杂-β3-氨基酸残基(氮杂-β3-aa)的简便通用方法。这些单体能够合成相对大量的纯混合氮杂-β3-肽。所需的Fmoc取代的氮杂-β3-氨基酸可通过简便的合成方法获得,并且已经合成了许多单体,包括那些含有带官能团侧链的单体。该方法应用于生物活性组蛋白H4序列的氮杂-β3-肽模拟物的固相合成。