Pd-catalyzed protecting-group-free cross-couplings of iodophenols with atom-economic triarylbismuth reagents
作者:Maddali L.N. Rao、Suresh Meka
DOI:10.1016/j.tetlet.2019.151512
日期:2020.2
An efficient protocol for the protecting-group-free synthesis of unsymmetrical hydroxybiaryls via the Pd-catalyzedcross-couplings of unprotected iodophenols with triarylbismuth reagents is described. The presented protocols exhibits good to high yields of hydroxybiaryls.
[EN] METHODS FOR PREPARING BRIDGED BI-AROMATIC LIGANDS<br/>[FR] PROCÉDÉS DE PRÉPARATION DE LIGANDS BI-AROMATIQUES PONTÉS
申请人:UNIVATION TECH LLC
公开号:WO2016172044A1
公开(公告)日:2016-10-27
New methods for preparing bridged bi-aromatic ligands are disclosed. The methods employ aryl coupling of unprotected phenols. The ligands may be used to prepare transition metal compounds useful as catalysts in olefin polymerization.
New methods for preparing bridged bi-aromatic ligands are disclosed. The methods employ aryl coupling of unprotected phenols. The ligands may be used to prepare transition metal compounds useful as catalysts in olefin polymerization.
Aryloxide ions (Ar'O-) behave as C-nucleophiles towards diazosulfides (ArN=NSR; R = Ph, But) leading to unsymmetrical hydroxybiaryls (ArAr'OH) via C-C coupling. The reaction is particularly suited for the synthesis of terms which contain electron-withdrawing groups on the Ar moiety. The SRN1 mechanism is proposed on the grounds of experimental evidences.