Results 21 to 30 of about 538,570 (408)

Visible-Light Assisted Covalent Surface Functionalization of Reduced Graphene Oxide Nanosheets with Arylazo Sulfones [PDF]

open access: yes, 2023
We present an environmentally benign methodology for the covalent functionalization (arylation) of reduced graphene oxide (rGO) nanosheets with arylazo sulfones. A variety of tagged aryl units were conveniently accommodated at the rGO surface via visible light irradiation of suspensions of carbon nanostructured materials in aqueous media. Mild reaction
arxiv   +1 more source

Aryl radical-mediated N-heterocyclic carbene catalysis

open access: yesNature Communications, 2021
There have been significant advancements in radical reactions using organocatalysts in modern organic synthesis. Recently, NHC-catalyzed radical reactions initiated by single electron transfer processes have been actively studied.
Yuki Matsuki   +6 more
semanticscholar   +1 more source

Efficient Copper-Catalyzed N-Arylation of Sulfoximines with Aryl Iodides and Aryl Bromides [PDF]

open access: yesThe Journal of Organic Chemistry, 2005
Two simple and inexpensive systems for copper-catalyzed N-arylations of sulfoximines with aryl bromides and aryl iodides have been developed. Using 10 mol % of a copper(I) salt in combination with 20 mol % of a 1,2-diamine and Cs2CO3 provides N-arylated sulfoximines in high yields. Various functional groups and heteroatoms are tolerated.
Joerg Sedelmeier, Carsten Bolm
openaire   +4 more sources

Anti-Proliferative and Cytoprotective Activity of Aryl Carbamate and Aryl Urea Derivatives with Alkyl Groups and Chlorine as Substituents

open access: yesMolecules, 2022
Natural cytokinines are a promising group of cytoprotective and anti-tumor agents. In this research, we synthesized a set of aryl carbamate, pyridyl urea, and aryl urea cytokinine analogs with alkyl and chlorine substitutions and tested their ...
Maxim Oshchepkov   +8 more
doaj   +1 more source

Potent Reductants via Electron-Primed Photoredox Catalysis: Unlocking Aryl Chlorides for Radical Coupling.

open access: yesJournal of the American Chemical Society, 2020
We describe a new catalytic strategy to transcend the energetic limitations of visible light by electrochemically priming a photocatalyst prior to excitation.
Nicholas G W Cowper   +3 more
semanticscholar   +1 more source

Nickel-catalyzed electrochemical carboxylation of unactivated aryl and alkyl halides with CO2

open access: yesNature Communications, 2021
Electrochemical catalytic reductive cross couplings are powerful and sustainable methods to construct C−C bonds by using electron as the clean reductant. However, activated substrates are used in most cases.
Guo-Quan Sun   +7 more
semanticscholar   +1 more source

ChemInform Abstract: Palladium‐Catalyzed α‐Arylation of Aryl Nitromethanes. [PDF]

open access: yesChemInform, 2015
AbstractThe straightforward reaction tolerates various aryl and hetaryl substituents except ortho‐substituted aryl groups.
Kelsey F. VanGelder, Marisa C. Kozlowski
openaire   +3 more sources

Synthesis of 2-aryl-benzothiazoles via Ni-catalyzed coupling of benzothiazoles and aryl sulfamates

open access: yesHeterocyclic Communications, 2020
2-Aryl-benzothiazoles have been successfully synthesized via a simple coupling reaction between benzothiazoles and aryl sulfamates using a nickel catalyst. The nickel catalyst is inexpensive, reusable and commercially available.
Yu Xiaofeng   +4 more
doaj   +1 more source

Visible-Light Photocatalytic Reduction of Aryl Halides as a Source of Aryl Radicals

open access: yesMolecules, 2022
Aryl- and heteroaryl units are present in a wide variety of natural products, pharmaceuticals, and functional materials. The method for reduction of aryl halides with ubiquitous distribution is highly sought after for late-stage construction of various ...
Jihong Lan   +4 more
doaj   +1 more source

Nickel-Mediated Hydrogenolysis of C–O Bonds of Aryl Ethers: What Is the Source of the Hydrogen? [PDF]

open access: yes, 2012
Mechanistic studies of the hydrogenolysis of aryl ethers by nickel were undertaken with (diphosphine)aryl methyl ethers. A Ni(0) complex containing Ni–arene interactions adjacent to the aryl–O bond was isolated.
Agapie, Theodor   +4 more
core   +3 more sources

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