Department of Chemistry, Seoul National University, Gwanak-1 Gwanak-ro, Gwanak-gu, Seoul, 08826, South Korea.
Angew Chem Int Ed Engl. 2019 Jan 8;58(2):488-493. doi: 10.1002/anie.201811530. Epub 2018 Dec 6.
Herein we report a novel synthetic entry to the legendary quinuclidine natural products quinine and quinidine. The developed strategy is based on the use of a symmetrical and nonstereogenic precursor to access quinine and quinidine through a "local-desymmetrization" approach, in stark contrast conceptually to the preparation of stereodefined disubstituted piperidines (or their acyclic precursors) as featured in all past syntheses. The developed strategy also provided quinine and quinidine derivatives that could not be readily obtained through previous total syntheses or by modification of the naturally occurring substances.
在此,我们报告了一种新型的合成方法,用于制备传奇的奎宁啶类天然产物奎宁和奎尼丁。所开发的策略基于使用对称且非手性的前体,通过“局部去对称化”方法来制备奎宁和奎尼丁,这与所有过去的合成方法中所采用的制备立体定义的二取代哌啶(或其无环前体)的概念形成鲜明对比。所开发的策略还提供了以前的全合成或对天然物质进行修饰无法轻易获得的奎宁和奎尼丁衍生物。