Exploring the selectivity of the Suzuki–Miyaura cross-coupling reaction in the synthesis of arylnaphthalenes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference19 articles.
1. The Palladium-Catalyzed Cross-Coupling Reaction of Phenylboronic Acid with Haloarenes in the Presence of Bases
2. Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds
3. Synthesis of Biaryls and Polyaryls by Ligand-Free Suzuki Reaction in Aqueous Phase
4. Computational Characterization of the Role of the Base in the Suzuki−Miyaura Cross-Coupling Reaction
5. A survey of Hammett substituent constants and resonance and field parameters
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1. Highlights on the General Preference for Multi-Over Mono-Coupling in the Suzuki–Miyaura Reaction;Catalysts;2023-05-24
2. Synthesis, conformational stability and molecular structure of 4-aryl- and 4,5-diaryl-1,8-bis(dimethylamino)naphthalenes;Organic & Biomolecular Chemistry;2023
3. 1,8‐Diarylnaphthalenes: Synthesis, Properties, and Applications;European Journal of Organic Chemistry;2022-12-20
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5. C(sp2)-C(sp2) Suzuki cross-coupling of arylammonium salts catalyzed by a stable Pd–NHC complex;Tetrahedron;2021-10
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