Institut für Organische Chemie, Gottfried Wilhelm Leibniz Universität Hannover, Schneiderberg 1B, 30167 Hannover, Germany.
Macromol Biosci. 2010 Sep 9;10(9):1028-33. doi: 10.1002/mabi.201000094.
In this paper we report the first synthesis of novel polysialic acid derivatives which is initiated by treatment of polysialic acid with EDC-HCl to yield the inter-residual delta-lactone. Subsequent reaction with amines or hydrazine gives the corresponding polysialic acid amides and hydrazide. Alkylation of the tetrabutylammonium salt of polysialic acid yields polysialic acid esters. In contrast a variety of N-derivatives of polysialic acid can be prepared starting from deacetylated polysialic acid. The N-derivatives prepared in this communication can be used for the Cu-catalyzed as well as Cu-free "click" chemistry.
本文首次报道了新型唾液酸衍生物的合成方法,该方法通过用 EDC-HCl 处理唾液酸来生成中间体 δ-内酸酐,然后与胺或肼反应得到相应的唾液酸酰胺和酰肼。用四丁基铵盐对唾液酸进行烷基化可得到唾液酸酯。相比之下,从去乙酰化的唾液酸可以制备各种唾液酸的 N-衍生物。本通讯中制备的 N-衍生物可用于铜催化和无铜“点击”化学。