Literature DB >> 30394634

A Local-Desymmetrization-Based Divergent Synthesis of Quinine and Quinidine.

Jaehoo Lee1, David Y-K Chen1.   

Abstract

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.
© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  alkaloids; desymmetrization; natural products; quinine; total synthesis

Year:  2018        PMID: 30394634     DOI: 10.1002/anie.201811530

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  2 in total

1.  Enantioselective total synthesis of the unnatural enantiomer of quinine.

Authors:  Shinya Shiomi; Remi Misaka; Mayu Kaneko; Hayato Ishikawa
Journal:  Chem Sci       Date:  2019-09-27       Impact factor: 9.825

2.  Early and Late Steps of Quinine Biosynthesis.

Authors:  Francesco Trenti; Kotaro Yamamoto; Benke Hong; Christian Paetz; Yoko Nakamura; Sarah E O'Connor
Journal:  Org Lett       Date:  2021-02-24       Impact factor: 6.005

  2 in total

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