Catalytic Synthesis of β‐(Hetero)arylethylamines: Modern Strategies and Advances

Author:

Pozhydaiev Valentyn1,Muller Cyprien1,Moran Joseph12ORCID,Lebœuf David1ORCID

Affiliation:

1. Institut de Science et d'Ingénierie Supramoléculaires (ISIS) CNRS UMR 7006 Université de Strasbourg 8 Allée Gaspard Monge 67000 Strasbourg France

2. Institut Universitaire de France (IUF) 75005 Paris France

Abstract

Abstractβ‐(Hetero)arylethylamines appear in a myriad of pharmaceuticals due to their broad spectrum of biological properties, making them prime candidates for drug discovery. Conventional methods for their preparation often require engineered substrates that limit the flexibility of the synthetic routes and the diversity of compounds that can be accessed. Consequently, methods that provide rapid and versatile access to those scaffolds remain limited. To overcome these challenges, synthetic chemists have designed innovative and modular strategies to access the β‐(hetero)arylethylamine motif, paving the way for their more extensive use in future pharmaceuticals. This review outlines recent progresses in the synthesis of (hetero)arylethylamines and emphasizes how these innovations have enabled new levels of molecular complexity, selectivity, and practicality.

Funder

Agence Nationale de la Recherche

Publisher

Wiley

Subject

General Medicine

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