Acceleration of Batch-type Heterogeneous Ligand-free Suzuki-Miyaura Reactions with Polymer Composite Supported Pd Catalyst
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-017-06499-z.pdf
Reference42 articles.
1. Miyaura, N., Yamada, K. & Suzuki, A. A new stereospecific cross-coupling by the palladium-catalyzed reaction of 1-alkenylboranes with 1-alkenyl or 1-alkynyl halides. Tetrahedron Lett. 20, 3437–3440 (1979).
2. Miyaura, N. & Suzuki, A. Stereoselective synthesis of arylated (E)-alkenes by the reaction of alk-1-enylboranes with aryl halides in the presence of palladium catalyst. Chem. Comm. 19, 866–867 (1979).
3. Suzuki, A. Synthetic Studies via the cross-coupling reaction of organoboron derivatives with organic halides. Pure Appl. Chem. 63, 419–422 (1991).
4. Miyaura, N. & Suzuki, A. Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds. Chem. Rev. 95, 2457–2483 (1995).
5. Suzuki, A. Recent advances in the cross-coupling reactions of organoboron derivatives with organic electrophiles. J. Organomet. Chem. 576, 147–168 (1999).
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