The interplay of carbophilic activation and Au (I)/Au (III) catalysis: an emerging technique for 1, 2-difunctionalization of C–C multiple bonds

VW Bhoyare, AG Tathe, A Das, CC Chintawar… - Chemical Society …, 2021 - pubs.rsc.org
Gold complexes have emerged as the catalysts of choice for various functionalization
reactions of C–C multiple bonds due to their inherent carbophilic nature. In a parallel space …

Recent advances in gold (III) chemistry: structure, bonding, reactivity, and role in homogeneous catalysis

L Rocchigiani, M Bochmann - Chemical Reviews, 2020 - ACS Publications
Over the past decade the organometallic chemistry of gold (III) has seen remarkable
advances. This includes the synthesis of the first examples of several compound classes that …

Dinuclear gold catalysis

W Wang, CL Ji, K Liu, CG Zhao, W Li… - Chemical Society Reviews, 2021 - pubs.rsc.org
Gold chemistry has developed extensively in the past decade, and a dozen good reviews
have been presented discussing this progress. Few however have paid close attention to …

Homogeneous gold redox chemistry: organometallics, catalysis, and beyond

B Huang, M Hu, FD Toste - Trends in chemistry, 2020 - cell.com
Gold redox chemistry holds the promise of unique reactivities and selectivities that are
different to other transition metals. Recent studies have utilized strain release, ligand design …

L‐Shaped Heterobidentate Imidazo[1,5‐a]pyridin‐3‐ylidene (N,C)‐Ligands for Oxidant‐Free AuI/AuIII Catalysis

P Gao, J Xu, T Zhou, Y Liu, E Bisz… - Angewandte Chemie …, 2023 - Wiley Online Library
In the last decade, major advances have been made in homogeneous gold catalysis.
However, AuI/AuIII catalytic cycle remains much less explored due to the reluctance of AuI to …

DFT-Enabled Development of Hemilabile (PN) Ligands for Gold(I/III) RedOx Catalysis: Application to the Thiotosylation of Aryl Iodides

K Muratov, E Zaripov, MV Berezovski… - Journal of the American …, 2024 - ACS Publications
Ligand-enabled oxidative addition of Csp2-X bonds to Au (I) centers has recently appeared
as a valuable strategy for the development of catalytic RedOx processes. Several cross …

A Hemilabile NHC‐Gold Complex and its Application to the Redox Neutral 1, 2‐Oxyarylation of Feedstock Alkenes

SC Scott, JA Cadge, GK Boden… - Angewandte Chemie …, 2023 - Wiley Online Library
We describe a AuI complex of a hemi‐labile (C^ N) N‐heterocyclic carbene ligand that is
able to mediate oxidative addition of aryl iodides. Detailed computational and experimental …

Gold (I)/Gold (III) Catalysis that Merges Oxidative Addition and π‐Alkene Activation

M Rigoulet, O Thillaye du Boullay… - Angewandte Chemie …, 2020 - Wiley Online Library
Heteroarylation of alkenes with aryl iodides was efficiently achieved with a (MeDalphos)
AuCl complex through AuI/AuIII catalysis. The possibility to combine oxidative addition of …

Unlocking Migratory Insertion in Gold Redox Catalysis

W Wang, M Ding, CG Zhao, S Chen… - Angewandte Chemie …, 2023 - Wiley Online Library
Exploration of elementary reactions in organometallic catalysis is an important method with
which to discover new reactions. In this article, we report a gold (I)‐catalyzed iodo …

Migratory insertion of CO into a Au–C bond

JA Cadge, PJ Gates, JF Bower… - Journal of the American …, 2022 - ACS Publications
A MeDalPhos-ligated gold (III) metallafluorene complex, generated via C–C oxidative
addition of biphenylene, reacts with CO to produce 9-fluorenone. Experimental and …