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放线内酯B的可扩展全合成

Scalable Total Synthesis of Acremolactone B.

作者信息

Ba Mengyu, He Fengqi, Ren Lu, Whittingham William G, Yang Peng, Li Ang

机构信息

College of Chemistry and Henan Institute of Advanced Technology, Zhengzhou University, Zhengzhou, 450001, China.

State Key Laboratory of Chemical Biology, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai, 200032, China.

出版信息

Angew Chem Int Ed Engl. 2024 Jul 15;63(29):e202314800. doi: 10.1002/anie.202314800. Epub 2024 Jun 17.

Abstract

Acremolactone B is a pyridine-containing azaphilone-type polyketide. The first total synthesis of this molecule was achieved on a gram scale, based on an aza-6π electrocyclization-aromatization strategy for construction of the tetra-substituted pyridine ring. A bicyclic intermediate was expeditiously prepared by using [2+2] photocycloaddition and chemoselective Baeyer-Villiger oxidation, which was further elaborated to a densely substituted aza-triene. An electrocyclization-aromatization cascade was utilized to forge the tetracyclic core of this natural product, and the side chain was introduced through diastereoselective acylation and reduction.

摘要

阿克莫内酯B是一种含吡啶的氮杂稠酮型聚酮化合物。基于构建四取代吡啶环的氮杂6π电环化-芳构化策略,首次实现了该分子的克级全合成。通过[2+2]光环化加成和化学选择性拜耳-维利格氧化快速制备了一个双环中间体,该中间体进一步转化为一个高度取代的氮杂三烯。利用电环化-芳构化串联反应构建了该天然产物的四环核心,并通过非对映选择性酰化和还原引入了侧链。

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