An alternative stereoselective total synthesis of (-)-pyrenophorol
收藏Taylor & Francis Group2019-08-06 更新2026-04-16 收录
下载链接：
https://tandf.figshare.com/articles/An_alternative_stereoselective_total_synthesis_of_-_-pyrenophorol/7981820/1
下载链接
链接失效反馈官方服务：
资源简介：
The total synthesis of 16-membered C<sub>2</sub>–Symmetric dilactone (-)-Pyrenophorol was accomplished starting from commercially available (<i>S</i>)<i>-</i>epoxide prepared by hydrolytic kinetic resolution of (±) – epoxide with key steps of Grignard reaction, Swern oxidation, Wittig reaction and cyclization was achieved by intermolecular Mitsunobu cyclization. The synthesis of (-)-Pyrenophorol accomplished from cheaply available starting material, easily work-up procedures and reduction of cost in industrial process were major advantages of this route.
提供机构：
Rudraraju Ramesh Raju; Choragudi Chandrasekhar; Gurrala Alluraiah; Reddymasu Sreenivasulu
创建时间：
2019-04-11
