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

González, Jorge A; Arribas, Andrés; Tian, Puyang; Díaz‐Alonso, Sergio; Mascareñas, José Luis; López, Fernando; Nevado, Cristina (2024). Gold(III) Auracycles Featuring C(sp$^3$)‐Au‐C(sp$^2$) Bonds: Synthesis and Mechanistic Insights into the Cycloauration Step. Angewandte Chemie Internationale Edition, 63(36):e202402798.

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.

Additional indexing

Item Type:Journal Article, refereed, original work
Communities & Collections:07 Faculty of Science > Department of Chemistry
Dewey Decimal Classification:540 Chemistry
Scopus Subject Areas:Physical Sciences > Catalysis
Physical Sciences > General Chemistry
Language:English
Date:2 September 2024
Deposited On:09 Feb 2025 16:07
Last Modified:10 Feb 2025 21:04
Publisher:Wiley-VCH Verlag
ISSN:1433-7851
OA Status:Hybrid
Publisher DOI:https://doi.org/10.1002/anie.202402798
PubMed ID:38776235
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  • Language: English
  • Licence: Creative Commons: Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)

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