Gold(III) Auracycles Featuring C(sp$^3$)‐Au‐C(sp$^2$) Bonds: Synthesis and Mechanistic Insights into the Cycloauration Step

The direct auration of arenes is a key step in numerous gold‐catalyzed reactions. Although reported more than 100 years ago, understanding of its underlying mechanism has been hampered by the difficulties in the isolation of relevant intermediates given the propensity of gold(III) species to undergo reductive elimination. Here, we report the synthesis and isolation of a new family of intriguing zwitterionic [C(sp$^{3}$)^C(sp$^{2}$)]‐auracyclopentanes, as well as of their alkyl‐gold(III) precursors and demonstrate their value as mechanistic probes to study the C(sp$^{2}$)‐Au bond‐forming event. Experimental investigations employing Kinetic Isotope Effects (KIE), Hammett plot, and Eyring analysis provided important insights into the formation of the auracycle. The data suggest a S$_{E}$Ar mechanism wherein the slowest step might be the π‐coordination between the arene and the gold(III) center, en route to the Wheland intermediate. We also show that these auracyclopentanes can work as catalysts in several gold‐promoted transformations.

Publication Details

Journal
Zurich Open Repository and Archive (University of Zurich)
Published
2024-09-02
DOI
https://doi.org/10.5167/uzh-274517
Primary Topic
Catalytic Alkyne Reactions
Type
article
Field-Weighted Citation Impact
0.00
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article

Gold(III) Auracycles Featuring C(sp$^3$)‐Au‐C(sp$^2$) Bonds: Synthesis and Mechanistic Insights into the Cycloauration Step

Zurich Open Repository and Archive (University of Zurich)
Catalytic Alkyne Reactions
article

Gold(III) Auracycles Featuring C(sp$^3$)‐Au‐C(sp$^2$) Bonds: Synthesis and Mechanistic Insights into the Cycloauration Step

article en

Abstract

The direct auration of arenes is a key step in numerous gold‐catalyzed reactions. Although reported more than 100 years ago, understanding of its underlying mechanism has been hampered by the difficulties in the isolation of relevant intermediates given the propensity of gold(III) species to undergo reductive elimination. Here, we report the synthesis and isolation of a new family of intriguing zwitterionic [C(sp$^{3}$)^C(sp$^{2}$)]‐auracyclopentanes, as well as of their alkyl‐gold(III) precursors and demonstrate their value as mechanistic probes to study the C(sp$^{2}$)‐Au bond‐forming event. Experimental investigations employing Kinetic Isotope Effects (KIE), Hammett plot, and Eyring analysis provided important insights into the formation of the auracycle. The data suggest a S$_{E}$Ar mechanism wherein the slowest step might be the π‐coordination between the arene and the gold(III) center, en route to the Wheland intermediate. We also show that these auracyclopentanes can work as catalysts in several gold‐promoted transformations.

Zurich Open Repository and Archive (University of Zurich)
Openalex Percentile: Top 71%
Catalytic Alkyne Reactions
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Gold(III) Auracycles Featuring C(sp$^3$)‐Au‐C(sp$^2$) Bonds: Synthesis and Mechanistic Insights into the Cycloauration Step · Zurich Open Repository and Archive (University of Zurich) (2024) | TGRS Research Map | TGRS