摘要
发展了一条改进的L-鸟嘌呤异核苷全合成路线.以L-核糖为起始原料,合成了3,5-O-二苄基-1-脱氧-L-核糖,再与碱基N2,N2-二叔丁氧羰基-6-氯鸟嘌呤发生关键的Mitsunobu反应来合成异核苷6.经过9步反应,以37.3%的总收率合成了L-鸟嘌呤异核苷,其中Mitsunobu反应构建异核苷键具有立体专一性、高产率、条件温和、区域选择性高等优点.该方法可以作为鸟嘌呤异核苷的通用合成路线.
An improved route for the total synthesis of iso-L-guanosine was developed. Using L-ribose as the starting material, 3,5-O-dibenzyl-1-deoxy-L-ribose was firstly synthesized. Then, Mitsunobu reaction between N2,N2-bis(tert-butyloxycarbonyl)-6-chloro-guanine and 3,5-O-dibenzyl-1-deoxy-L-ribose afforded isonucleoside 6. Finally, iso-L-guanosine was synthesized in 9 steps with 37.3% overall yield. Adopting Mitsunobu reaction as the key step, it has the merits of high steroseletivity and regioselectivity, mild reaction condition, and high yield. Currently developed approach could be used as a general synthetic strategy for the synthesis other related guanine isonucleosides.
作者
唐杰
董祥有
欧阳文良
朱云龙
丁海新
肖强
Tang Jie;Dong Xiangyou;Ouyang Wenliang;Zhu Yunlong;Ding Haixin;Xiao Qiang(Jiangxi Key Laboratory of Organic Chemistry, Institute of Organic chemistry, Jiangxi Science & Technology Normal University, Nanchang 330013)
出处
《有机化学》
SCIE
CAS
CSCD
北大核心
2019年第9期2609-2615,共7页
Chinese Journal of Organic Chemistry
基金
国家自然科学基金(Nos.21462019,21676131)
江西省科技厅重点(No.20143ACB20012)
江西科技师范大学博士启动基金(No.2018BSQD022)资助项目~~
