RECENT ADVANCES IN THE TOTAL SYNTHESIS OF CLAVILACTONES

被引：1
|
作者：
Ogura, Akihiro [1 ]
Takao, Ken-ichi [1 ]
机构：
[1] Keio Univ, Dept Appl Chem, Kohoku Ku, Yokohama, Kanagawa 2238522, Japan
来源：
HETEROCYCLES | 2020年 / 100卷 / 09期
关键词：
CATALYZED CARBONYLATION-PEROXIDATION; RING-CLOSING METATHESIS; STRUCTURE ELUCIDATION; FRAGMENTATION; CYCLIZATION; ALDEHYDES; REVISION; ACCESS;
D O I：
10.3987/REV-20-928
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
Clavilactones are meroterpenoids containing a 10-membered carbocycle fused to an alpha,beta-epoxy-gamma-lactone and a hydroquinone or benzoquinone. This review describes the total synthesis of clavilactones achieved by four research groups, focusing on their innovative synthetic strategies.
引用
收藏
页码：1355 / 1370
页数：16
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