Recent Developments in the Syntheses of C-20-Oxygenated ent-Kaurane Diterpenoids

被引:2
|
作者
Yue, Guizhou [1 ]
Liu, Bo [2 ]
机构
[1] Sichuan Agr Univ, Coll Sci, Xinkang Rd 46, Yaan 625014, Sichuan, Peoples R China
[2] Sichuan Univ, Coll Chem, 29 Wangjiang Rd, Chengdu 610064, Sichuan, Peoples R China
来源
CHEMPLUSCHEM | 2024年 / 89卷 / 06期
关键词
natural product; diterpenoid; ent-kaurane; semi-synthesis; total synthesis; ANTI-HIV PRINCIPLE; TRIPTERYGIUM-WILFORDII; UNIFIED STRATEGY; NATURAL-PRODUCTS; AIDS AGENTS; ISODON; LACTONES; KAURENE; ORIDONIN;
D O I
10.1002/cplu.202300676
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Ent-kaurane diterpenes are a large group of natural products, with more than 1,000 compounds since their discovery. Due to their excellent biological activities and complex polycyclic structures, these compounds have attracted organic synthesis chemists around the world to be devoted to achieve their total synthesis. At present, the isolated C-20-oxygenated ent-kaurane diterpenes are the most abundant of these natural products, reaching more than 350 in number. However, only total syntheses of 3,20-epoxy, 7,20-epoxy and 19,20-lactone ent-kaurane diterpenes have been reported. In this review, we elaborate the synthesis of these three types of C-20 oxygenated ent-kaurane natural products, discuss these synthetic strategies in detail, and provide good guidance and reference for the synthesis of other C-20 oxygenated compounds.
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页数:11
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