Transition metal-free synthesis of α-aryl ketones via oxyallyl cation capture with arylboronic acids

WH Huang, GB Huang, WR Zhu, J Weng… - Organic Chemistry …, 2020 - pubs.rsc.org
Herein, we describe a novel transition metal-free, umpolung strategy for the α-arylation of
ketones by capturing transient oxyallyl cations with arylboronic acids. A variety of α-arylated …

Synthesis of bis-quaternary centers at the α-positions of cyclohexanones via Copper (I)-Catalyzed Claisen rearrangement: The substituent effect from the opposing α …

SC Philkhana, JA Malone, E Armendariz-Gonzalez… - Tetrahedron, 2025 - Elsevier
We report the synthesis of bis-quaternary centers at the α-positions of cyclohexanones. In
this chemistry, ionization of an α-hydroxy allyl vinyl ether with Cu (MeCN) 4 BF 4 catalyst at …

Brønsted Acid‐Catalyzed Intramolecular α‐Arylation of Ketones with Phenolic Nucleophiles via Oxy‐Allyl Cation Intermediates

Y Aota, Y Doko, T Kano… - European Journal of …, 2020 - Wiley Online Library
Nucleophilic addition to the oxy‐allyl cation intermediate has emerged as a promising
methodology for functionalization of the α‐position of carbonyl compounds in an umpolung …

[PDF][PDF] Reversing the Regioselectivity of Indole Addition to Cyclic Unsymmetrical Oxyallyl Cations: Construction of Diaryl Quaternary Centers

TD Curry II - 2021 - repository.lsu.edu
1. Purpose The purpose of this research discussion is to first carry out a literature review on
the discovery and utility of oxyallyl cation intermediates. Oxyallyl cation intermediates …