Literature DB >> 33955153

Synthesis of Morphinans through Anodic Aryl-Aryl Coupling.

Nina Vierengel1, Leander Geske1, Eisuke Sato1, Till Opatz1.   

Abstract

The morphinans are an important class of structurally fascinating and physiologically important natural products as exemplified by the famous opium alkaloids of the morphine family. Although this class of secondary metabolites from the juice of the opium poppy capsule was already used for medicinal purposes thousands of years ago, chemical modifications are still being applied to the core structure today in order to achieve the most specific effect on the various receptor subtypes possible with the fewest possible side effects. The unusual architecture of the morphinan core has also proven to be a highly challenging target for total synthesis. This review highlights electrosynthetic approaches towards natural and semisynthetic morphinan alkaloids. The historical progress in applying anodic aryl-aryl couplings to the construction of the morphinan framework is described in chronological order while particular benefits and challenges concerning the electrochemical transformations are grouped together, including the influence of substitution patterns, protecting groups, and reaction conditions.
© 2021 The Authors. Published by The Chemical Society of Japan & Wiley-VCH GmbH.

Entities:  

Keywords:  Electrochemistry; anodic oxidation; aryl-aryl coupling; morphinans; total synthesis

Year:  2021        PMID: 33955153     DOI: 10.1002/tcr.202100078

Source DB:  PubMed          Journal:  Chem Rec        ISSN: 1528-0691            Impact factor:   6.771


  1 in total

1.  A General Electro-Synthesis Approach to Amaryllidaceae Alkaloids.

Authors:  Dennis Pollok; Luca M Großmann; Torsten Behrendt; Till Opatz; Siegfried R Waldvogel
Journal:  Chemistry       Date:  2022-07-13       Impact factor: 5.020

  1 in total

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