Enantioselective C-H amination catalyzed by homoleptic iron salox complexes.

Iron complexes bearing chiral salicyloxazoline (Salox) ligands catalyze the enantioselective intramolecular C-H bond amination of alkyl azides, reaching 58-76% ee for benzylic C-H bonds. Further, for the first time aliphatic C-H bond amination is demonstrated (∼40% ee). This class of catalysts even activates primary aliphatic C-H bonds, albeit with moderate ee.

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Publication Details

Journal
Open Access CRIS of the University of Bern
Published
2025-09-08
DOI
https://doi.org/10.48620/91196
Primary Topic
Geochemistry and Geologic Mapping
Type
article
Field-Weighted Citation Impact
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article

Enantioselective C-H amination catalyzed by homoleptic iron salox complexes.

Open Access CRIS of the University of Bern
Geochemistry and Geologic Mapping
article

Enantioselective C-H amination catalyzed by homoleptic iron salox complexes.

article en

Abstract

Iron complexes bearing chiral salicyloxazoline (Salox) ligands catalyze the enantioselective intramolecular C-H bond amination of alkyl azides, reaching 58-76% ee for benzylic C-H bonds. Further, for the first time aliphatic C-H bond amination is demonstrated (∼40% ee). This class of catalysts even activates primary aliphatic C-H bonds, albeit with moderate ee.

Open Access CRIS of the University of Bern
GP Forschungsgruppe (DE), Pharmaceutical Biotechnology (Czechia) (CZ)
Openalex Percentile: Top 49%
Geochemistry and Geologic Mapping
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Enantioselective C-H amination catalyzed by homoleptic iron salox complexes. · Open Access CRIS of the University of Bern (2025) | TGRS Research Map | TGRS