Shamim Anwar, Souza Frederico B, Trossini Gustavo H G, Gatti Fernando M, Stefani Hélio A
Instituto de Química, Universidade de São Paulo, São Paulo, SP, Brazil.
Mol Divers. 2015 Aug;19(3):423-34. doi: 10.1007/s11030-014-9564-0. Epub 2015 Jan 14.
We have developed an efficient, CuI-catalyzed, microwave-assisted method for the synthesis of bis-1,2,3-triazole derivatives starting from a 3,4,6-tri-O-acetyl-D-glucal-derived mesylate. This mesylate was obtained from 3,4,6-tri-O-acetyl-D-glucal through C-glycosidation, deprotection of acetate groups to alcohols, and selective mesylation of the primary alcohol. This mesylate moiety was then converted to an azide through a microwave-assisted method with good yield. The azide, once synthesized, was then treated with different terminal alkynes in the presence of CuI to synthesize various bis-triazoles in high yields and short reaction times.
我们开发了一种高效的、碘化亚铜催化的、微波辅助的方法,用于从3,4,6-三-O-乙酰基-D-葡糖醛衍生的甲磺酸酯开始合成双-1,2,3-三唑衍生物。该甲磺酸酯是通过C-糖苷化、将乙酸酯基团脱保护为醇以及伯醇的选择性甲磺酰化从3,4,6-三-O-乙酰基-D-葡糖醛获得的。然后通过微波辅助方法将该甲磺酸酯部分高产率地转化为叠氮化物。一旦合成了叠氮化物,便在碘化亚铜存在下用不同的末端炔烃处理,以高产率和短反应时间合成各种双三唑。