Bio-inspired formal total synthesis of (±)-bisabosqual A

被引:1
|
作者
Du, Xuanxuan [1 ]
Liu, Hainan [1 ]
Wu, Yumeng [1 ]
Tang, Yu [1 ,2 ]
机构
[1] Ocean Univ China, Sch Med & Pharm, Key Lab Marine Drugs, Chinese Minist Educ, Qingdao 266003, Peoples R China
[2] Pilot Natl Lab Marine Sci & Technol, Lab Marine Drugs & Bioprod, Qingdao 266237, Peoples R China
基金
中国国家自然科学基金;
关键词
SQUALENE SYNTHASE INHIBITORS; CYCLOADDITION APPROACH; BIOMIMETIC SYNTHESIS; TETRACYCLIC CORE; BISABOSQUALS; SYSTEM;
D O I
10.1039/d2qo01697d
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A new approach was developed to construct a hexahydrobenzofurobenzopyran ring system (6/6/5/6) by an oxa-[3 + 3] cycloaddition, intramolecular hetero-Diels-Alder reaction, oxidative aromatization, and oxidative cyclization cascade starting from 5-(hydroxymethyl)cyclohexane-1,3-dione and (2E,6E)-farnesal. This strategy provides a new solution for preparing tetracyclic hexahydrobenzofurobenzopyran rings with different functional groups at C-3 '-C4 '. As a synthetic application, the bio-inspired formal total synthesis of bisabosqual A was achieved.
引用
收藏
页码:1042 / 1046
页数:5
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