![PDF] Palladium and visible-light mediated carbonylative Suzuki-Miyaura coupling of unactivated alkyl halides and aryl boronic acids. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/c034f60b31c3fb8bde9e474d05e355610aac1e4a/2-Table1-1.png "PDF] Palladium and visible-light mediated carbonylative Suzuki-Miyaura coupling of unactivated alkyl halides and aryl boronic acids. | Semantic Scholar")
PDF] Palladium and visible-light mediated carbonylative Suzuki-Miyaura coupling of unactivated alkyl halides and aryl boronic acids. | Semantic Scholar
Palladium-Catalyzed Hydroxylation of Aryl Halides with Boric Acid | Organic Letters
Palladium-Catalyzed Hydroxylation of Aryl Halides with Boric Acid | Organic Letters
Palladium-Catalyzed, Direct Boronic Acid Synthesis from Aryl Chlorides: A Simplified Route to Diverse Boronate Ester Derivatives | Journal of the American Chemical Society
Scheme 5 Possible side reactions with Pd catalysts in the reaction of... | Download Scientific Diagram
Suzuki-Miyaura cross-coupling of phenylboronic acid with aryl halides catalyzed by palladium and nickel species supported on alumina-based oxides - ScienceDirect
Catalysts | Free Full-Text | Microwave-Assisted Palladium-Catalyzed Cross-Coupling Reactions: Generation of Carbon–Carbon Bond
Palladium-catalyzed borylation of aryl (pseudo)halides and its applications in biaryl synthesis | BMC Chemistry | Full Text
Suzuki reaction of phenylboronic acid with aryl halides in the presence... | Download Table
Comparison between reactions. (a) aryl halide (1.1 mmol), arylboronic... | Download Scientific Diagram
A new palladium precatalyst allows for the fast Suzuki-Miyaura coupling reactions of unstable polyfluorophenyl and 2-heteroaryl boronic acids. | Semantic Scholar
Palladium‐Catalyzed Direct Arylation of (Hetero)Arenes with Aryl Boronic Acids - Yang - 2008 - Angewandte Chemie International Edition - Wiley Online Library
BJOC - Palladium(II)-catalyzed Heck reaction of aryl halides and arylboronic acids with olefins under mild conditions
Catalysts | Free Full-Text | Recent Advances in Metal-Catalyzed Alkyl–Boron (C(sp3)–C(sp2)) Suzuki-Miyaura Cross-Couplings
Suzuki coupling between phenylboronic acid and aryl halides. The... | Download Scientific Diagram
Palladium-Catalyzed Hydroxylation of Aryl Halides with Boric Acid | Organic Letters
![PDF] Room-temperature palladium-catalysed Suzuki–Miyaura coupling of arylboric acid with aryl chlorides | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/ddca6ac6a0773a85249c99e02c2f39093ca4d16e/3-Table1-1.png "PDF] Room-temperature palladium-catalysed Suzuki–Miyaura coupling of arylboric acid with aryl chlorides | Semantic Scholar")
PDF] Room-temperature palladium-catalysed Suzuki–Miyaura coupling of arylboric acid with aryl chlorides | Semantic Scholar
Suzuki cross-coupling of structurally different aryl halides and... | Download Table
Coupling of Aryl Halides with Aryl Boronic Acids with P(C6H5)(2-C6H4Cl)2 as the Supporting Ligand | Organometallics
Palladium-Catalyzed Hydroxylation of Aryl Halides with Boric Acid | Organic Letters
![PDF] Palladium and visible-light mediated carbonylative Suzuki-Miyaura coupling of unactivated alkyl halides and aryl boronic acids. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/c034f60b31c3fb8bde9e474d05e355610aac1e4a/1-Figure1-1.png "PDF] Palladium and visible-light mediated carbonylative Suzuki-Miyaura coupling of unactivated alkyl halides and aryl boronic acids. | Semantic Scholar")
PDF] Palladium and visible-light mediated carbonylative Suzuki-Miyaura coupling of unactivated alkyl halides and aryl boronic acids. | Semantic Scholar
Palladium-Catalyzed Hydroxylation of Aryl Halides with Boric Acid
Coupling of Aryl Halides with Aryl Boronic Acids with P(C6H5)(2-C6H4Cl)2 as the Supporting Ligand | Organometallics
Palladium-Catalyzed Hydroxylation of Aryl Halides with Boric Acid | Organic Letters
BJOC - Palladium-catalyzed solid-state borylation of aryl halides using mechanochemistry
Recent advances in transition metal-catalysed cross-coupling of (hetero)aryl halides and analogues under ligand-free conditions - Catalysis Science & Technology (RSC Publishing) DOI:10.1039/C9CY01331H
