A highly active palladium(II)-bis(oxazoline) catalyst for Suzuki-Miyaura, Mizoroki-Heck and sonogashira coupling reactions in aqueous dimethylformamide
Author:
Affiliation:
1. Chemistry Department; King Fahd University of Petroleum & Minerals; Dhahran 31261 Saudi Arabia
2. Institut Sciences Chimiques de Rennes; UMR 6226, CNRS, Université de Rennes 1; France
Funder
Unit at King Fahd University of Petroleum & Minerals
Publisher
Wiley
Subject
Inorganic Chemistry,General Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/aoc.3305/fullpdf
Reference44 articles.
1. Palladium Nanoparticles on Graphite Oxide: A Recyclable Catalyst for the Synthesis of Biaryl Cores
2. Rapid and Amenable Suzuki Coupling Reaction in Water Using Microwave and Conventional Heating
3. Acrylic monomers and polymers with perfluoroalkylated biphenyl side groups: synthesis and phase transitions
4. Carbon–carbon bonding made easy
5. Pd(l-proline)2complex: an efficient catalyst for Suzuki-Miyaura coupling reaction in neat water
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2. A comparative study of catalytic activity on iron‐based carbon nanostructured catalysts with Pd loading: Using the Box–Behnken design (BBD) method in the Suzuki–Miyaura coupling;Applied Organometallic Chemistry;2021-09-09
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4. Recent Advances in Synthesis and Uses of Heterocycles-based Palladium(II) Complexes as Robust, Stable, and Low-cost Catalysts for Suzuki- Miyaura Crosscouplings;Current Organic Chemistry;2019-10-28
5. Efficient N-heterocyclic carbene palladium(II) catalysts for carbonylative Suzuki-Miyaura coupling reactions leading to aryl ketones and diketones;Journal of Organometallic Chemistry;2018-03
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