Division of Organic Chemistry, Combi Chem-Bio Resource Center, National Chemical Laboratory, Pune, 411008, India.
Org Biomol Chem. 2011 Sep 7;9(17):5951-9. doi: 10.1039/c1ob05056g. Epub 2011 Apr 12.
Propargyl 1,2-O-orthoesters are exploited for the synthesis of 1,2-trans O-glycosides of protected amino acids. N-Fmoc- and N-Cbz protected serine/threonine - benzyl/methyl esters reacted well with glucosyl-, galactosyl-, mannosyl- and lactosyl- derived propargyl 1,2-orthoesters affording respective 1,2-trans glycosides in good yields under AuBr(3)/4 Å MS Powder/CH(2)Cl(2)/rt. t-Boc serine derivative gave serine 1,2-orthoester and glycosyl carbamate. Optimized conditions enabled preparation of new glycosyl carbamates from N-Boc protected amines in a single step using gold catalysts and propargyl 1,2-orthoesters in excellent yields.
炔丙基 1,2-O-原酸酯被用于合成保护的氨基酸的 1,2-顺式 O-糖苷。N-Fmoc-和 N-Cbz 保护的丝氨酸/苏氨酸-苄基/甲酯与葡萄糖基、半乳糖基、甘露糖基和乳糖基衍生的炔丙基 1,2-原酸酯反应良好,在 AuBr(3)/4 Å MS 粉末/CH(2)Cl(2)/rt 下分别以良好的收率得到相应的 1,2-顺式糖苷。t-Boc 丝氨酸衍生物得到丝氨酸 1,2-原酸酯和糖基氨基甲酸酯。优化条件使使用金催化剂和炔丙基 1,2-原酸酯可以从 N-Boc 保护的胺一步制备新的糖基氨基甲酸酯,收率优异。