摘要
以D-甘露糖为原料,通过乙酰化、去乙酰化、苯亚甲基化、硅基化等8步反应合成了6-氧-叔丁基二甲基硅基-2,4-二-氧-苯甲酰基-3-氧-对甲氧基苄基-α-D-甘露吡喃糖乙硫苷,总收率21.7%,其结构经~1H NMR,^(13)C NMR,IR和LC-MS(ESI)确证。
Ethyl-2,4-di-O-benzoyl-3-O-p-methoxybenzyl-6-O-tert-butyldimethyl silyl-1-thio-α-D-mannopyranoside was synthesized from D-Mannose by eight-step of acetylation,deactylation,benzylidenation,silylation,etc,with an overall yield of 21. 7%. The structure was confirmed by^1H NMR,^13C NMR,IR and LC-MS(ESI).
作者
张飞
周颖钰
储悦
雷进才
杨劲松
ZHANGFei;ZH;CHUYue;LEI Jin-cai;YANG Jin-song(West China School of Pharmacy,Sichuan University,Chengdu 610041,China)
出处
《合成化学》
CAS
CSCD
北大核心
2018年第7期490-493,共4页
Chinese Journal of Synthetic Chemistry
基金
国家自然科学基金资助项目(21372166)