5,7‐Membered Cyclometallated Gold(III) Complexes with Pyridine‐Phenyl‐Oxazoline N^C^N Ligands as Catalysts for Organic Transformation Reactions Under Silver‐Free Conditions

A series of 5,7‐membered cyclometallated gold(III) complexes with N^C^N tridentate ligands are developed as catalysts, which are prepared via transmetalation of pyridine‐phenyl‐oxazoline ligand‐containing organomercury compounds with potassium gold(III) chloride (KAuCl 4 ) with up to 86% yields. Investigation on the synthesis and catalytic activity of the newly developed gold(III) complexes under silver‐free conditions results in >90% conversion for propargylamines and up to >99% conversion for bifunctional modification of oligosaccharides via three‐component (A 3 )‐coupling reactions. Employment of the tridentate gold(III) complexes also successfully catalyzes the carboalkoxylation reaction of acetal alkynes. These results reveal potential applications of such 5,7‐membered tridentate gold(III) complexes as catalysts for organic transformation reactions and modification of biomolecules.

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Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2025-08-21
DOI
https://doi.org/10.1002/adsc.70038
Primary Topic
Catalytic Alkyne Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

5,7‐Membered Cyclometallated Gold(III) Complexes with Pyridine‐Phenyl‐Oxazoline N^C^N Ligands as Catalysts for Organic Transformation Reactions Under Silver‐Free Conditions

Man‐Kin Wong, Karen Ka‐Yan Kung, A. Chan, Nathanael Chun‐Him Lai et al.
Advanced Synthesis & Catalysis
Catalytic Alkyne Reactions
article

5,7‐Membered Cyclometallated Gold(III) Complexes with Pyridine‐Phenyl‐Oxazoline N^C^N Ligands as Catalysts for Organic Transformation Reactions Under Silver‐Free Conditions

Man‐Kin Wong, Karen Ka‐Yan Kung, A. Chan, Nathanael Chun‐Him Lai, Yosephine Tania Limanto
article en

Abstract

A series of 5,7‐membered cyclometallated gold(III) complexes with N^C^N tridentate ligands are developed as catalysts, which are prepared via transmetalation of pyridine‐phenyl‐oxazoline ligand‐containing organomercury compounds with potassium gold(III) chloride (KAuCl 4 ) with up to 86% yields. Investigation on the synthesis and catalytic activity of the newly developed gold(III) complexes under silver‐free conditions results in >90% conversion for propargylamines and up to >99% conversion for bifunctional modification of oligosaccharides via three‐component (A 3 )‐coupling reactions. Employment of the tridentate gold(III) complexes also successfully catalyzes the carboalkoxylation reaction of acetal alkynes. These results reveal potential applications of such 5,7‐membered tridentate gold(III) complexes as catalysts for organic transformation reactions and modification of biomolecules.

Advanced Synthesis & CatalysisVol. 367(17)
Hong Kong Polytechnic University (HK)
Hong Kong Polytechnic University
Openalex Percentile: Top 84%
Catalytic Alkyne Reactions
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