药学研究
藥學研究
약학연구
Journal of Pharmaceutical Research
2015年
12期
741-743
,共3页
5 - 氧 - 烯丙基 - 2,3,4 - 三 - 氧 - 苄基 - D - 核糖醇%合成%抗体%核糖 - 核糖醇
5 - 氧 - 烯丙基 - 2,3,4 - 三 - 氧 - 芐基 - D - 覈糖醇%閤成%抗體%覈糖 - 覈糖醇
5 - 양 - 희병기 - 2,3,4 - 삼 - 양 - 변기 - D - 핵당순%합성%항체%핵당 - 핵당순
5 - Allyloxy - 2,3,4 - tris(benzyloxy)pentan - 1 - ol%Synthesis%Antibody%Ribose - ribitol
目的:合成5-氧-烯丙基-2,3,4-三-氧-苄基- D -核糖醇。方法以 D -核糖为原料,经甲苷化、苄基化、水解、肟保护、烯丙基化、脱肟、还原7步反应得到5-氧-烯丙基-2,3,4-三-氧-苄基- D -核糖醇。结果与讨论总收率55%,目标产物结构经核磁共振氢谱确认。该合成路线步骤少,绿色环保,适合工业化生产。
目的:閤成5-氧-烯丙基-2,3,4-三-氧-芐基- D -覈糖醇。方法以 D -覈糖為原料,經甲苷化、芐基化、水解、肟保護、烯丙基化、脫肟、還原7步反應得到5-氧-烯丙基-2,3,4-三-氧-芐基- D -覈糖醇。結果與討論總收率55%,目標產物結構經覈磁共振氫譜確認。該閤成路線步驟少,綠色環保,適閤工業化生產。
목적:합성5-양-희병기-2,3,4-삼-양-변기- D -핵당순。방법이 D -핵당위원료,경갑감화、변기화、수해、우보호、희병기화、탈우、환원7보반응득도5-양-희병기-2,3,4-삼-양-변기- D -핵당순。결과여토론총수솔55%,목표산물결구경핵자공진경보학인。해합성로선보취소,록색배보,괄합공업화생산。
Objective To synthesize 5 - allyloxy - 2,3,4 - tris(benzyloxy)pentan - 1 - ol. Methods With D - ri-bose as the starting material,5 - allyloxy - 2,3,4 - tris(benzyloxy)pentan - 1 - ol was obtained by glycosidation,benzyla-tion,hydrolyzation,oxime protection,allylation,deoximation and reduction. Results and Conclusion The overall yield of this method was 55% ,and the structure of product was characterized by 1H - NMR. The synthetic route was short and envi-ronmentally friendly,suitable for the industrial production.