C–H functionalization of aromatic amines for azidation catalyzed by Betti base coordinated copper(ii) complexes under ultrasonication DOI

G. Premkumar,

Toka Swu,

Richa Gupta

и другие.

New Journal of Chemistry, Год журнала: 2023, Номер 47(33), С. 15677 - 15685

Опубликована: Янв. 1, 2023

Five new Betti base copper( ii ) complexes (C1–C5) are successfully synthesized and characterized spectroscopically.

Язык: Английский

An Efficient Supported Cu(I) Catalyst for the Amination of Aryl Halides with Sodium Azide DOI

Somayeh Fekri,

Yagoub Mansoori, Yüksel Akınay

и другие.

ChemNanoMat, Год журнала: 2024, Номер 10(6)

Опубликована: Март 27, 2024

Abstract We present the synthesis and characterization of a new Cu(I) complex supported on SBA‐15 as catalyst for preparing anilines from reaction aryl halides with sodium azide. The support was modified by treating it sequentially (3‐aminopropyl) triethoxysilane (APTES), cyanuric chloride, 2‐aminothiazole (AT). mesoporous silica, SBA‐15@BAT, then treated CuI solution in acetonitrile to give SBA‐15@BAT‐Cu(I). underwent thorough using conventional methods. X‐Ray photoelectron spectroscopy (XPS) analysis corroborated presence copper +1 oxidation state catalyst. sufficiently catalyzed amination iodo‐, bromo‐, chloroarenes NaN 3 . centrifuged, washed, applied subsequent run. investigated effects various components parameters determine optimal conditions reaction. heterogeneous exhibited noticeable stability reused over seven runs slight deactivation.

Язык: Английский

Процитировано

1

Catalysed Aryl Amine Syntheses via Azides: From Azidation of Aryl Halides to Azide Reduction and Direct Amination DOI Creative Commons
Max Roemer

ChemCatChem, Год журнала: 2024, Номер unknown

Опубликована: Май 6, 2024

Abstract This review summarises and discusses aryl amine azide syntheses from halides employing azides. The majority of the reported reactions proceed with copper catalysis or mediation. Often, an is formed in first step, which then reduced situ to a second step. occurrence reduction, depends on chosen reaction conditions substrates. formation only azides through Cu‐mediated C−N bond formations discussed, followed by mediated catalytic reduction different systems, azidation amines, viz . azidation‐amination strategies. allows for synthesis complex heterocycles multi‐step one‐pot procedures, several are summarised here. Examples application synthesising important amines employed as biologically active compounds, materials science also summarised. Finally, conducted control have been collected discussed combination mechanistic proposals. literature survey us pinpoint design criteria valuable includes choice such solvent system additives, involved metal promising

Язык: Английский

Процитировано

1

Azide-Assisted Growth of Copper Nanostructures and Their Application as a Carbon Supported Catalyst in Two-Step Three-Component Azide–Alkyne Cycloadditions DOI
Max Roemer, William Lewis

Langmuir, Год журнала: 2023, Номер 39(38), С. 13560 - 13570

Опубликована: Авг. 16, 2023

Copper nanostructures were obtained from the reduction of Cu(I) under mild conditions in ethanol/water using sodium-l-ascorbate and sodium azide while performing an amination reaction. When halobenzene substrate was reacted presence a bulk carbon black (CB) support, clustered copper sub-micrometer particles (SMPs) microparticles (MPs) form. The growth MPs optimized, supported isolated characterized by scanning electron microscopy, energy dispersive X-ray spectroscopy, thermogravimetry, inductively-coupled plasma mass spectrometry. are mobile within CB matrix proved to be active catalysts azide–alkyne cycloaddition (CuAAC). catalytic competency assessed two-step three-component benzyl bromide, azide, phenylacetylene as model reaction optimized applied for synthesis triazole compounds with varying levels functionalization. recyclability investigated, depletion modes discussed, fine-tuned reach good recyclability. This demonstrates broader applicability SMPs/MPs CuAAC-catalyst its limitations.

Язык: Английский

Процитировано

3

C–H functionalization of aromatic amines for azidation catalyzed by Betti base coordinated copper(ii) complexes under ultrasonication DOI

G. Premkumar,

Toka Swu,

Richa Gupta

и другие.

New Journal of Chemistry, Год журнала: 2023, Номер 47(33), С. 15677 - 15685

Опубликована: Янв. 1, 2023

Five new Betti base copper( ii ) complexes (C1–C5) are successfully synthesized and characterized spectroscopically.

Язык: Английский

Процитировано

0