Recent Progress Toward Total Syntheses of Iheyamines A and B

被引:0
作者
Kim, Tae Lyn [1 ]
Jeon, Jiye [1 ]
Lee, Yong Ho [1 ]
Cheon, Cheol-Hong [1 ]
机构
[1] Korea Univ, Dept Chem, 145 Anam ro, Seoul 02841, South Korea
基金
新加坡国家研究基金会;
关键词
iheyamines A and B; total synthesis; azepinobisindoles; alkaloids; natural products; CATALYZED ALLYLIC ALKYLATION; INDOLE-3-ACETIC-ACID DERIVATIVES; SKELETON;
D O I
10.1002/ajoc.202300513
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
This perspective article describes the recent progress in the total syntheses of iheyamines A and B. Since iheyamine A possesses a highly unique unsymmetrical azepino-2,2'-bisindole scaffold, novel strategies to construct the basic scaffold have been developed, and unique total syntheses have been reported based on these strategies. In addition, because iheyamine B bears vicinal 2-oxopropyl moieties with a trans-configuration in the azepine scaffold of iheyamine A, the first asymmetric total synthesis of iheyamine B took a substantially longer time than iheyamine A to complete. Due to the unusual structure of iheyamine B and some discrepancies in the experimental data between the isolated and synthesized iheyamine B, some controversial issues regarding whether iheyamine B is a natural product or an artifact have been raised and will be discussed. This perspective provides an overview of the recent progress in the total synthesis of iheyamines A and B, including the development of novel strategies to access the unique structural features of these natural products. In addition, controversial issues regarding whether iheyamine B is a natural product or an artifact are discussed.image
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页数:11
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