Substituted Dihydropyridine Synthesis by Dearomatization of Pyridines

Heusler, Arne; Fliege, Julian; Wagener, Tobias; Glorius, Frank

Research article (journal) | Peer reviewed

Abstract

Dearomatization is an effective method to transform readily available N-heterocycles into partially saturated motifs. Manipulation of dihydro-derivatives holds great potential and provides access to a variety of semi-saturated N-heterocyclic building blocks. However, current strategies are limited in scope and the use of sensitive reagents restricts the applicability in synthetic laboratories. Herein, we report the synthesis of a broad variety of N-substituted 1,4- and 1,2-dihydropyridines by very mild and selective reduction with amine borane for the first time.

Details about the publication

JournalAngewandte Chemie International Edition (Angew. Chem. Int. Ed.)
Volume60
Issue25
Page range13793-13797
StatusPublished
Release year2021
Language in which the publication is writtenEnglish
DOI10.1002/anie.202104115
Link to the full texthttps://onlinelibrary.wiley.com/doi/10.1002/anie.202104115
Keywordsboranes; chemoselectivity; nitrogen heterocycles; reduction; synthetic methods; dearomatizations

Authors from the University of Münster

Fliege, Julian
Organic Chemistry Institute
Glorius, Frank
Professur für Organische Chemie (Prof. Glorius)
Heusler, Arne
Professur für Organische Chemie (Prof. Glorius)
Wagener, Tobias
Professur für Organische Chemie (Prof. Glorius)