Mild and Low-Pressure<i>fac</i>-Ir(ppy)<sub>3</sub>-Mediated Radical Aminocarbonylation of Unactivated Alkyl Iodides through Visible-Light Photoredox Catalysis
作者:Shiao Y. Chow、Marc Y. Stevens、Linda Åkerbladh、Sara Bergman、Luke R. Odell
DOI:10.1002/chem.201601694
日期:2016.6.27
unactivated alkyl iodides employing a fac‐Ir(ppy)3‐catalyzed radical aminocarbonylation protocol has been developed. Using a two‐chambered system, alkyl iodides, fac‐Ir(ppy)3, amines, reductants, and CO gas (released ex situ from Mo(CO)6), were combined and subjected to an initial radical reductive dehalogenation generating alkyl radicals, and a subsequent aminocarbonylation with amines affording a
Tandem Photoredox Catalysis: Enabling Carbonylative Amidation of Aryl and Alkylhalides
作者:José A. Forni、Nenad Micic、Timothy U. Connell、Geethika Weragoda、Anastasios Polyzos
DOI:10.1002/anie.202006720
日期:2020.10.12
visible‐light‐mediated carbonylative amidation of aryl, heteroaryl, and alkyl halides. A tandem catalytic cycle of [Ir(ppy)2(dtb‐bpy)]+ generates a potent iridium photoreductant through a second catalytic cycle in the presence of DIPEA, which productively engages aryl bromides, iodides, and even chlorides as well as primary, secondary, and tertiary alkyl iodides. The versatile in situ generated catalyst is compatible
Nickel/Photoredox-Catalyzed Amidation via Alkylsilicates and Isocyanates
作者:Shuai Zheng、David N. Primer、Gary A. Molander
DOI:10.1021/acscatal.7b02795
日期:2017.11.3
A nickel/photoredox, dual-catalyzed amidationreaction between alkylsilicate reagents and alkyl/aryl isocyanates is reported. In contrast to the previously reported reductive coupling process, this protocol is characterized by mild reaction conditions and the absence of a stoichiometric reductant. A mechanistic hypothesis involving a nickel-isocyanate adduct is proposed based on literature precedent