摘要
目的改进单糖给体构件块的合成方法。方法单糖经过全苯甲酰基化、溴代、水解,与三氯乙腈生成三氯乙酰亚胺酯的活性给体。结果与结论合成的4种醛基糖的三氯乙酰亚胺酯的活性给体收率达到w=80%左右,其结构经过1H-NMR1、3C-NMR确证。
Objective To improve the synthetic method of monosaccharide donor moiety. Methods Four monosaccharide trichloroacetimidates donors were prepared through benzoylation, bromination, hydrolysis, and addition with trichloroacetonitrile in about 80 % yield. Rusults and Conclusions All products were determined by ^1H-NMR and ^13C-NMR. This simple method provides high yield in preparation of monosacchride donors with aldoses.
出处
《沈阳药科大学学报》
CAS
CSCD
北大核心
2005年第5期352-354,共3页
Journal of Shenyang Pharmaceutical University
基金
国家自然科学基金资助项目(30028023)