Total Synthesis of Atisane-Type Diterpenoids: Application of Diels鈥揂lder Cycloadditions of Podocarpane-Type Unmasked ortho-Benzoquinones

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• 作者：Liqiang Song ; Guili Zhu ; Yongjiang Liu ; Bo Liu ; Song Qin
• 刊名：Journal of the American Chemical Society
• 出版年：2015
• 出版时间：October 28, 2015
• 年：2015
• 卷：137
• 期：42
• 页码：13706-13714
• 全文大小：756K
• ISSN：1520-5126

文摘

Few examples of [4 + 2] cycloaddition with unmasked ortho-benzoquinones (UMOBs) as carbodiene have been reported in complex molecule synthesis. Herein we report that this cycloaddition with podocarpane-type UMOB was developed and applied to construct fully functionalized bicyclo[2.2.2]octanes. Based on this methodology, divergent total syntheses of atisane-type diterpenoids, including (卤)-crotobarin, crotogoudin, atisane-3尾,16伪-diol, and 16S,17-dihydroxy-atisan-3-one, were accomplished in 14, 14, 12, and 16 steps, respectively. Key elements in these total syntheses include: (1) FeCl₃-catalyzed cationic cascade cyclization to construct podocarpane-type skeleton; (2) Mn(III)/Co(II)-catalyzed radical hydroxylation of alkene with high regio-, diastereo-, and chemoselectivities; (3) and a ketal-deprotection/lactone-opening/deprotonation/lactonization cascade. Additionally, the synthetic utility of the fully functionalized bicyclo[2.2.2]octane framework was further elucidated by applying ring distortion strategy to afford different skeleton-rearranged natural product-like compounds.