Synthesis of α-Quaternary Aldehydes via a Dual Ni/Rh-Catalyzed Tandem Isomerization–Propargylation Reaction

A dual Ni/Rh catalysis sequence toward α-quaternary aldehydes is reported. An intramolecular approach from allyl propargyl carbonates alongside the intermolecular transformation from allylic alcohols and propargyl carbonates is described. Initial decarboxylative oxidative addition into the propargyl group by nickel generates the electrophilic Ni–allenyl species, and the resulting allylic alkoxide is isomerized into the nucleophilic Rh–enolate species. Upon recombination, the α-propargylated aldehyde is obtained. Preliminary enantioselective results are reported, with varying protocols using either a dual metal single ligand or a dual metal dual ligand system.

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Publication Details

Journal
ACS Catalysis
Published
2024-10-08
DOI
https://doi.org/10.1021/acscatal.4c05021
Citations
3
Primary Topic
Catalytic Alkyne Reactions
Type
article
Field-Weighted Citation Impact
0.75

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article

Synthesis of α-Quaternary Aldehydes via a Dual Ni/Rh-Catalyzed Tandem Isomerization–Propargylation Reaction

Eun Seo Choi, Mark Lautens, Justin Ching, Megan Jaschinski
3 citations
ACS Catalysis
Catalytic Alkyne Reactions
0.75
article

Synthesis of α-Quaternary Aldehydes via a Dual Ni/Rh-Catalyzed Tandem Isomerization–Propargylation Reaction

Eun Seo Choi, Mark Lautens, Justin Ching, Megan Jaschinski
article en
3 citations

Abstract

A dual Ni/Rh catalysis sequence toward α-quaternary aldehydes is reported. An intramolecular approach from allyl propargyl carbonates alongside the intermolecular transformation from allylic alcohols and propargyl carbonates is described. Initial decarboxylative oxidative addition into the propargyl group by nickel generates the electrophilic Ni–allenyl species, and the resulting allylic alkoxide is isomerized into the nucleophilic Rh–enolate species. Upon recombination, the α-propargylated aldehyde is obtained. Preliminary enantioselective results are reported, with varying protocols using either a dual metal single ligand or a dual metal dual ligand system.

ACS CatalysisVol. 14(20)
University of Toronto (CA)
University of Toronto, Kennarshore, Natural Sciences and Engineering Research Council of Canada
Openalex Percentile: Top 32%
Catalytic Alkyne Reactions
0.75
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