Laboratoire des Matériaux Polymères et des Biomatériaux, Ingénierie des Matériaux Polymères, UMR CNRS 5223, Université Lyon 1, Domaine scientifique de La Doua, Bât. ISTIL, 15 Bd Latarjet, F-69622 Villeurbanne Cedex, France.
Carbohydr Res. 2010 Aug 16;345(12):1685-97. doi: 10.1016/j.carres.2010.05.010. Epub 2010 May 19.
The total chemical synthesis of the four well-defined chitodisaccharides is described using N-trichloroacetyl (TCA) and N-benzyloxycarbonyl (Z) as C-2 protecting groups for acetamido and free amino groups, respectively. The synthesis is carried out according to a strategy that paves way to the elaboration of various homo- and hetero-chitooligosaccharides, with perfect control of the number and the position of GlcN and GlcNAc units along the oligomer chain.
本文描述了使用 N-三氯乙酰基(TCA)和 N-苄氧羰基(Z)作为 C-2 乙酰氨基和游离氨基的保护基团,对四种结构明确的壳二糖进行全化学合成。该合成策略为各种同型和异型壳寡糖的制备铺平了道路,可精确控制寡糖链上 GlcN 和 GlcNAc 单元的数量和位置。