School of Physical and Chemical Sciences, University of Canterbury, Private Bag 4800, Christchurch 8140, New Zealand.
Org Lett. 2023 Mar 24;25(11):1989-1993. doi: 10.1021/acs.orglett.3c00584. Epub 2023 Mar 13.
Unprotected sugars are selectively acetylated simply by stirring in aqueous solution in the presence of acetic anhydride and a weak base such as sodium carbonate. The reaction is selective for acetylation of the anomeric hydroxyl group of mannose, 2-acetamido, and 2-deoxy sugars and can be performed on a large scale. Competitive intramolecular migration of the 1--acetate to the 2-hydroxyl group when these two substituents are causes over-reaction and the formation of product mixtures.
未保护的糖在醋酸酐和弱碱(如碳酸钠)存在下于水溶液中搅拌即可被选择性乙酰化。该反应对甘露糖、2-乙酰氨基和 2-脱氧糖的端基羟基的乙酰化具有选择性,并且可以在大规模上进行。当这两个取代基是时,1--醋酸酯向 2-羟基的竞争分子内迁移会导致过度反应和产物混合物的形成。