4.8 Article

Cover Picture: Expedient Synthesis of Bridged Bicyclic Nitrogen Scaffolds via Orthogonal Tandem Catalysis (Angew. Chem. Int. Ed. 40/2021)

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 60, Issue 40, Pages 21597-21597

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202109132

Keywords

alkenylation; bridged bicyclic nitrogen scaffolds; normorphan; remote functionalization; tandem catalysis

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Increasing saturation is beneficial for successful drug development, while bridged nitrogen heterocycles show great potential in drug discovery despite the need for long synthetic sequences. New efficient and selective organic synthesis methods are highly desired.
Escape from flatland. Increased saturation (fraction of sp(3)) is more likely to be successful when moving compounds through the drug development pipeline. Bridged nitrogen heterocycles have a huge potential in drug discovery, although long synthetic sequences are typically required. New step-economic and selective organic syntheses are therefore highly sought after. Bert U. W. Maes et al. describe in their Research Article on page 21988 the synthesis of the normorphan skeleton through challenging tandem catalysis. Cover design by Joris Snaet.+

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