Copper‐Catalyzed Arylation of Olefins Using a Novel N,N‐Bidentate TRAM‐Based Ligand: Application in Synthesis of Functionalized Triarylmethanes[]**
Author:
Affiliation:
1. Department of Chemistry Vali-e-Asr University of Rafsanjan Rafsanjan 77176, Islamic Republic of Iran Iran
2. NMR Laboratory Faculty of Science Vali-e-Asr University of Rafsanjan Rafsanjan 77176, Islamic Republic of Iran Iran
Funder
Vali-e-Asr University of Rafsanjan
Publisher
Wiley
Subject
General Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/slct.202102158
Reference131 articles.
1. Substituted Functional Olefins Through Lateral Sequential Lithiation/Silylation/Condensation of Tertiary Aromatic Amides: A Ligand for Phosphane-Free Palladium-Catalyzed Suzuki Coupling Reactions
2. Bis-quinoline-2-carboxylic acid Copper Salt as an Efficient Catalyst for Synthesis of Aryl Olefins by Heck Reaction
3. Highly Efficient Heck Reactions of Aryl Bromides with n-Butyl Acrylate Mediated by a Palladium/Phosphine−Imidazolium Salt System
4. Triaryl phosphine-functionalized N-heterocyclic carbene ligands for Heck reaction
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3. Site-selective nucleophilic substitution reactions of pentafluoropyridine with hydroxybenzaldehydes: synthesis of triarylmethanes comprising perfluoropyridine moieties;New Journal of Chemistry;2023
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