Double C–H bond functionalization for C–C coupling at the β-position of thiophenes using palladium-catalyzed 1,4-migration associated with direct arylation
Author:
Affiliation:
1. Univ. Rennes, 35042 Rennes, France
Abstract
Funder
Centre National de la Recherche Scientifique
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2023/QO/D3QO00018D
Reference74 articles.
1. Carboxylate-Assisted Transition-Metal-Catalyzed C−H Bond Functionalizations: Mechanism and Scope
2. Ruthenium(II)-Catalyzed C–H Bond Activation and Functionalization
3. Orthogonal Palladium-Catalyzed Direct C−H Bond Arylation of Heteroaromatics with Aryl Halides
4. Ru-catalysed C–H functionalisations as a tool for selective organic synthesis
5. Palladium-catalyzed benzofuran and indole synthesis by multiple C–H functionalizations
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1. Regiodivergent C–H alkynylation of 2-arylthiazoles switched by RuII and PdII catalysis;Chemical Communications;2024
2. Synthesis of Heteroarylated Pyridines via a Double C−H Bond Functionalization using Palladium‐catalyzed 1,4‐Migration Combined with Direct Arylation;ChemCatChem;2023-12-20
3. Palladium‐Catalyzed Heck Type Regioselective β‐Vinylation of Thiophenes Using a Bromo Substituent as Traceless Directing Group;European Journal of Organic Chemistry;2023-12-14
4. Catalyst-controlled regiodivergent C–H bond alkenylation of 2-pyridylthiophenes;Chemical Communications;2023
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