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钯催化的立体选择性氮杂-Wacker-Heck 环化反应:一步法多步策略合成四环稠合杂环。

Palladium-Catalyzed Stereoselective Aza-Wacker-Heck Cyclization: One-Pot Stepwise Strategy toward Tetracyclic Fused Heterocycles.

机构信息

School of Pharmacy, China Medical University, Taichung 406040, Taiwan.

Department of Medical Applied Chemistry, Chung Shan Medical University, Taichung 40201, Taiwan.

出版信息

Org Lett. 2020 Dec 4;22(23):9337-9341. doi: 10.1021/acs.orglett.0c03552. Epub 2020 Nov 23.

Abstract

Palladium-catalyzed intramolecular tandem cyclization reactions were conducted for the synthesis of densely /fused aza-tetracyclic structures. The process involved a palladium(II)-catalyzed aerobic aza-Wacker reaction, followed by a palladium(0)-catalyzed Heck reaction. The effects of the solvent and benzene substitution pattern on the one-pot, two-step cascade reaction were studied systematically, and a probable mechanism was proposed. Strained pentahydrobenzo[]cyclopenta[]indolizin-6-one and racemic γ-lycorane can also be synthesized rapidly using this palladium-catalyzed aza-Wacker-Heck cyclization reaction.

摘要

钯催化的分子内串联环化反应被用于合成稠合的氮杂四环结构。该过程涉及钯(II)催化的有氧氮杂-Wacker 反应,接着是钯(0)催化的 Heck 反应。系统研究了溶剂和苯取代模式对一锅两步级联反应的影响,并提出了一种可能的机理。使用这种钯催化的氮杂-Wacker-Heck 环化反应,也可以快速合成应变的五氢苯并[]环戊[]吲哚嗪-6-酮和外消旋γ-石蒜碱。

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