Total synthesis of natural products containing benzofuran rings

被引:141
作者
Heravi, Majid M. [1 ]
Zadsirjan, Vahideh [1 ]
Hamidi, Hoda [1 ]
Amiri, Parvin Hajiabbas Tabar [1 ]
机构
[1] Alzahra Univ, Dept Chem, Sch Sci, Tehran, Iran
基金
新加坡国家研究基金会;
关键词
FISCHER CARBENE COMPLEXES; 1ST TOTAL-SYNTHESIS; RESISTANT STAPHYLOCOCCUS-AUREUS; N-PHENYLPYRAZOLE DERIVATIVES; PALLADIUM-CATALYZED REACTION; PHOTO-FRIES REARRANGEMENT; CROSS-COUPLING REACTIONS; FUNGUS PHELLINUS-RIBIS; CARBON BOND FORMATION; ONE-POT SYNTHESIS;
D O I
10.1039/c7ra03551a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Research on natural products containing benzofuran has remarkably increased during the past few decades. Newly isolated natural products with complex structures are being studied, characterized and screened for possible biological activities. Several of such compounds have exhibited various biological activities, thus their total syntheses have attracted much attention from synthetic organic chemists. In this review, we aim to highlight the origins, structures, biological potencies, and synthetic approaches of those natural products bearing at least one benzofuran in their complex structures. Furthermore, we especially focus on the step in which this key heterocycle is installed during the total synthesis of a natural product as the desired target.
引用
收藏
页码:24470 / 24521
页数:52
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