Total Synthesis of a Marine Macrolide Natural Product, Iriomoteolide-2a: The Fundamental Role of Total Synthesis in Natural Product Chemistry

被引:2
作者
Sakamoto, Keita [1 ]
Fuwa, Haruhiko [1 ]
机构
[1] Chuo Univ, Dept Appl Chem, Bunkyo Ku, 1-13-27 Kasuga, Tokyo 1128551, Japan
关键词
marine natural product; macrolide; structure determination; biological evaluation; CROSS-COUPLING REACTIONS; UNIVERSAL NMR DATABASES; STEREOCHEMICAL ASSIGNMENT; STRUCTURE REVISION; DESERTOMYCIN/OASOMYCIN CLASS; ABSOLUTE-CONFIGURATION; BIOLOGICAL EVALUATION; STRUCTURAL REVISION; ACYCLIC COMPOUNDS; PRACTICAL METHOD;
D O I
10.5059/yukigoseikyokaishi.77.831
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Marine macrolide natural products are an important source of new chemotherapeutics and their lead compounds. Although in recent years significant advances of NMR instruments have enabled structure determination of natural products at sub-microgram scale, complex macrolides are still challenging targets for structure assignment because many of them contain multiple stereogenic centers along conformationally flexible macrocyclic backbone. Accordingly, total synthesis plays a conclusive role in structure determination of complex tnacrolides. Furthermore, biological assessment of synthetic material is indispensable for validating the biological activity/potency of natural products. In this paper, we delineate our total synthesis of a marine macrolide iriomoteolide-2a as a case study that demonstrates the significance of total synthesis in natural product chemistry.
引用
收藏
页码:831 / 840
页数:10
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