An expedient, mild and aqueous method for Suzuki–Miyaura diversification of (hetero)aryl halides or (poly)chlorinated pharmaceuticals
Author:
Affiliation:
1. School of Chemistry and BSRC, University of St Andrews, St Andrews, KY16 9ST, UK
Abstract
Funder
FP7 Ideas: European Research Council
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2021/QO/D1QO00919B
Reference28 articles.
1. Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds
2. Selected Patented Cross-Coupling Reaction Technologies
3. Palladium-catalyzed alkylations in aqueous media
4. Mixed phosphine/N-heterocyclic carbene palladium complexes: synthesis, characterization and catalytic use in aqueous Suzuki–Miyaura reactions
5. Palladium-catalyzed Suzuki reaction in aqueous solvents applied to unprotected nucleosides and nucleotides
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2. The role of phosphines in the activations of coupled substrates in the Suzuki—Miyaura reaction;Russian Chemical Bulletin;2024-03
3. Replacing polar aprotic solvents with water in organic synthesis;Current Opinion in Green and Sustainable Chemistry;2023-04
4. Active Pd intermediates of the Suzuki-Miyaura reaction with low reactive aryl chlorides under “ligand-free” conditions;Molecular Catalysis;2023-04
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