Divergent Synthesis of 17-nor-Cephalotane Diterpenoids through Developed Ynol-diene Cyclization
点击次数:
影响因子:16.1
DOI码:10.1002/anie.202407757
发表刊物:Angew. Chem. Int. Ed.
摘要:17-nor-Cephalotane diterpenoids include two categories, Cephalotaxus troponoids and tropone-free 17-nor-cephalotane diterpenoids, which possess polycyclic frameworks with seven-membered A ring bearing different oxidation states. We report herein a novel ynoldiene cyclization as a rapid access to tropone unit. Combining with a bioinspired stereoselective dual hydrogenation, the first divergent strategy to both categories of 17-nor-cephalotane diterpenoids has been successfully established, which enabled the total synthesis of Cephalotaxus troponoids, (+)-3-deoxyfortalpinoid F and (+)-harringtonolide, and tropone-free 17-nor-cephalotane diterpenoids, (−)-fortalpinoids M/N/P and analog (−)-20-deoxocephinoid P, in 14-17 linear longest steps starting from commercially available materials.
论文类型:期刊论文
页面范围:e202407757
是否译文:否
收录刊物:SCI
发布期刊链接:https://onlinelibrary.wiley.com/doi/full/10.1002/anie.202407757
通讯作者:胡向东