Abstract
AbstractAn efficient stereoselective semi-synthesis of (+)-digitoxigenin has been achieved by a nine-step sequence with a 20.4% overall yield. The key features of the synthesis include a Saegusa–Ito oxidation reaction, a direct C14β-hydroxylation, and a Stille cross-coupling.
Funder
Fundamental Research Funds for the Central Universitie
National Natural Science Foundation of China
Cited by
2 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献