Robust Acenaphthoimidazolylidene Palladacycles: Highly Efficient Catalysts for the Amination of N-Heteroaryl Chlorides

Chemistry - An Asian Journal - Germany
doi 10.1002/asia.201701055
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Wiley

Related search

Highly Efficient Low-Temperature N-Doped TiO2 Catalysts for Visible Light Photocatalytic Applications

Materials
Materials ScienceCondensed Matter Physics
2018English

Bimetallic Ag-Pt Sub-Nanometer Supported Clusters as Highly Efficient and Robust Oxidation Catalysts

Angewandte Chemie - International Edition
CatalysisChemistry
2017English

Water-Soluble Palladacycles as Precursors to Highly Recyclable Catalysts for the Suzuki Coupling of Aryl Bromides in Aqueous Solvents

English

N-Boc-O-Tosyl Hydroxylamine as a Safe and Efficient Nitrogen Source for the N-Amination of Aryl and Alkyl Amines: Electrophylic Amination

Synlett
Organic Chemistry
2011English

A Highly Active Catalyst for Pd-Catalyzed Amination Reactions: Cross-Coupling Reactions Using Aryl Mesylates and the Highly Selective Monoarylation of Primary Amines Using Aryl Chlorides

Journal of the American Chemical Society
BiochemistryColloidCatalysisChemistrySurface Chemistry
2008English

Mild and General Methods for the Palladium-Catalyzed Cyanation of Aryl and Heteroaryl Chlorides

English

H3PW12O40: Highly Efficient Catalysts for the Synthesis of Novel 1,3,5- Triaryl-2-Pyrazoline Derivatives

The Open Catalysis Journal
2010English

Supported Gold(III) Catalysts for Highly Efficient Three-Component Coupling Reactions

Angewandte Chemie
2008English

Highly Efficient Ruthenium Catalysts for the Formation of Tetrasubstituted Olefins via Ring-Closing Metathesis.

ChemInform
2007English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy