A concise synthesis of herbertenolide

被引:2
|
作者
Hu, Jiadong [1 ]
Ji, Kai [2 ]
Yan, Lihong [2 ]
Yang, Siyu [2 ]
Li, Yin [2 ]
Wen, Wen [1 ]
Chen, Le [2 ]
Wu, Xiaohui [2 ]
Hu, Youcai [3 ]
Xie, Weiqing [2 ,4 ]
机构
[1] Yangling Vocat & Tech Coll, Sch Med & Chem Engn, 24 Weihui Rd, Yangling 712100, Shaanxi, Peoples R China
[2] Northwest A&F Univ, Sch Pharm & Chem, Shaanxi Key Lab Nat Prod & Chem Biol, 22 Xinong Rd, Yangling 712100, Shaanxi, Peoples R China
[3] Chinese Acad Med Sci, Peking Union Med Coll, Inst Mat Med, State Key Lab Bioact Subst & Funct Nat Med, Beijing, Peoples R China
[4] Key Lab Bot Pesticide R&D Shaanxi Prov, Yangling 712100, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
CARBON CENTERS; CONSTRUCTION; SESQUITERPENOIDS; (+/-)-HERBERTENOLIDE; GENERATION; REACTIVITY; PALLADIUM;
D O I
10.1039/d2ob00041e
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A concise synthesis of (+/-)-herbertenolide has been accomplished herein. The strategy relies on a H2O2-mediated oxidative ring contraction of all-substituted cyclic alpha-formyl ketones for the stereospecific construction of contiguous quaternary carbon centers (CQCCs). Furthermore, a Sc(OTf)(3)/chiral N,N '-dioxide catalyzed asymmetric Michael addition of benzofuranone to MVK has been optimized for forging a chiral aromatic quaternary carbon center, which enables the formal synthesis of (+)-ent-herbertenolide.
引用
收藏
页码:2205 / 2208
页数:4
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