Gold-Catalyzed Migratory Insertion of Alkynes

Migratory insertion is a key elementary step within organometallic chemistry, frequently encountered with most transition metals. However, in the realm of gold catalysis, the migratory insertion step has remained elusive for a long time. Herein, we disclose the migratory insertion of alkynes into Au(III)–C bonds in a catalytic fashion. Experimental results suggest that the migratory insertion pathway predominates over the π-activation pathway, a finding further supported by the Density Functional Theory (DFT) calculations. The observed regioselectivity underscores the distinct advantages and complementarity of gold catalysis in comparison with palladium catalysis. Furthermore, the utility of the protocol has been demonstrated for the synthesis of various Polycyclic Aromatic Hydrocarbons (PAHs) via Scholl’s reaction.

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Publication Details

Journal
ACS Catalysis
Published
2025-04-29
DOI
https://doi.org/10.1021/acscatal.5c01141
Citations
4
Primary Topic
Catalytic Alkyne Reactions
Type
article
Field-Weighted Citation Impact
3.74

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article

Gold-Catalyzed Migratory Insertion of Alkynes

Nitin T. Patil, Avishek Das, Vincent Gandon, Biswajit Biswas
4 citations
ACS Catalysis
Catalytic Alkyne Reactions
3.74
article

Gold-Catalyzed Migratory Insertion of Alkynes

Nitin T. Patil, Avishek Das, Vincent Gandon, Biswajit Biswas
article en
4 citations

Abstract

Migratory insertion is a key elementary step within organometallic chemistry, frequently encountered with most transition metals. However, in the realm of gold catalysis, the migratory insertion step has remained elusive for a long time. Herein, we disclose the migratory insertion of alkynes into Au(III)–C bonds in a catalytic fashion. Experimental results suggest that the migratory insertion pathway predominates over the π-activation pathway, a finding further supported by the Density Functional Theory (DFT) calculations. The observed regioselectivity underscores the distinct advantages and complementarity of gold catalysis in comparison with palladium catalysis. Furthermore, the utility of the protocol has been demonstrated for the synthesis of various Polycyclic Aromatic Hydrocarbons (PAHs) via Scholl’s reaction.

ACS CatalysisVol. 15(10)
Centre National de la Recherche Scientifique (FR), Université Paris-Saclay (FR), Indian Institute of Science Education and Research, Bhopal (IN), Institut de Chimie Moléculaire et des Matériaux d'Orsay (FR)
University Grants Commission, Centre National de la Recherche Scientifique, Université Paris-Saclay, Indian Institute of Science Education and Research Bhopal, Science and Engineering Research Board
Openalex Percentile: Top 8%
Catalytic Alkyne Reactions
3.74
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