Chiral Triazole-Substituted Iodonium Salts in Enantioselective Halogen Bond Catalysis

Herein, we present the synthesis of chiral triazole-based diaryliodonium salts and their application as monodentate asymmetric iodine(III) derivates in halogen bond (XB) catalyzed reactions. These potential Lewis acids were successfully benchmarked in the vinylogous Mannich reaction of cyanomethyl coumarin with isatin-derived ketimine to obtain the addition product in up to 99% yield and >99:1 e.r. Furthermore, these halogen bond catalysts allowed an efficient functionalization of ketimines with various alcohols toward N,O-acetals in up to 99% yield and 90:10 e.r. Additionally, we studied the origin of the enantioselectivity based on density functional theory (DFT) and the catalyst crystal structure. These unveiled an approach of asymmetric induction facilitated by using σ-hole stabilized chiral moieties in iodine(III)-based catalysts, predominantly predicated upon XB activation.

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Publication Details

Journal
ACS Catalysis
Published
2024-12-18
DOI
https://doi.org/10.1021/acscatal.4c06895
Citations
17
Primary Topic
Oxidative Organic Chemistry Reactions
Type
article
Field-Weighted Citation Impact
4.25

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article

Chiral Triazole-Substituted Iodonium Salts in Enantioselective Halogen Bond Catalysis

Daniel Duvinage, Tim Stauch, Mattis Damrath, Tarek Scheele et al.
17 citations
ACS Catalysis
Oxidative Organic Chemistry Reactions
4.25
article

Chiral Triazole-Substituted Iodonium Salts in Enantioselective Halogen Bond Catalysis

Daniel Duvinage, Tim Stauch, Mattis Damrath, Tarek Scheele, Boris J. Nachtsheim
article en
17 citations

Abstract

Herein, we present the synthesis of chiral triazole-based diaryliodonium salts and their application as monodentate asymmetric iodine(III) derivates in halogen bond (XB) catalyzed reactions. These potential Lewis acids were successfully benchmarked in the vinylogous Mannich reaction of cyanomethyl coumarin with isatin-derived ketimine to obtain the addition product in up to 99% yield and >99:1 e.r. Furthermore, these halogen bond catalysts allowed an efficient functionalization of ketimines with various alcohols toward N,O-acetals in up to 99% yield and 90:10 e.r. Additionally, we studied the origin of the enantioselectivity based on density functional theory (DFT) and the catalyst crystal structure. These unveiled an approach of asymmetric induction facilitated by using σ-hole stabilized chiral moieties in iodine(III)-based catalysts, predominantly predicated upon XB activation.

ACS CatalysisVol. 15(1)
University of Bremen (DE), Instituto de Física Teórica (ES), Institute of Crystallography (IT)
Deutsche Forschungsgemeinschaft
Openalex Percentile: Top 5%
Oxidative Organic Chemistry Reactions
4.25
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Chiral Triazole-Substituted Iodonium Salts in Enantioselective Halogen Bond Catalysis — Daniel Duvinage, Tim Stauch, et al. · ACS Catalysis (2024) | TGRS Research Map | TGRS