![Post-transcriptional labeling by using Suzuki-Miyaura cross-coupling generates functional RNA probes. - Abstract - Europe PMC Post-transcriptional labeling by using Suzuki-Miyaura cross-coupling generates functional RNA probes. - Abstract - Europe PMC](https://europepmc.org/articles/PMC6009664/bin/gky185fig7.jpg)
Post-transcriptional labeling by using Suzuki-Miyaura cross-coupling generates functional RNA probes. - Abstract - Europe PMC
Suzuki homo-coupling reaction based fluorescent sensors for monosaccharides - RSC Advances (RSC Publishing)
![A highly selective and sensitive boronic acid-based sensor for detecting Pd2+ ion under mild conditions - ScienceDirect A highly selective and sensitive boronic acid-based sensor for detecting Pd2+ ion under mild conditions - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0960894X20305084-ga1.jpg)
A highly selective and sensitive boronic acid-based sensor for detecting Pd2+ ion under mild conditions - ScienceDirect
![Suzuki homo-coupling reaction based fluorescent sensors for monosaccharides - RSC Advances (RSC Publishing) DOI:10.1039/C4RA07331B Suzuki homo-coupling reaction based fluorescent sensors for monosaccharides - RSC Advances (RSC Publishing) DOI:10.1039/C4RA07331B](https://pubs.rsc.org/image/article/2014/RA/c4ra07331b/c4ra07331b-s1_hi-res.gif)
Suzuki homo-coupling reaction based fluorescent sensors for monosaccharides - RSC Advances (RSC Publishing) DOI:10.1039/C4RA07331B
Immobilized boronic acid for Suzuki–Miyaura coupling: application to the generation of pharmacologically relevant molecules - RSC Advances (RSC Publishing)
![Molecules | Free Full-Text | Boronic Acids and Their Derivatives in Medicinal Chemistry: Synthesis and Biological Applications | HTML Molecules | Free Full-Text | Boronic Acids and Their Derivatives in Medicinal Chemistry: Synthesis and Biological Applications | HTML](https://www.mdpi.com/molecules/molecules-25-04323/article_deploy/html/images/molecules-25-04323-sch009.png)
Molecules | Free Full-Text | Boronic Acids and Their Derivatives in Medicinal Chemistry: Synthesis and Biological Applications | HTML
![Palladium‐Catalyzed Tandem Reaction of Quinazolinone‐Based Nitriles with Arylboronic Acids: Synthesis of 2‐(4‐Arylquinazolin‐2‐yl)anilines - Zhang - 2018 - Advanced Synthesis & Catalysis - Wiley Online Library Palladium‐Catalyzed Tandem Reaction of Quinazolinone‐Based Nitriles with Arylboronic Acids: Synthesis of 2‐(4‐Arylquinazolin‐2‐yl)anilines - Zhang - 2018 - Advanced Synthesis & Catalysis - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/f2e2c39c-ddb6-493f-b9ab-b87f8473b0c0/adsc201800615-toc-0001-m.jpg)
Palladium‐Catalyzed Tandem Reaction of Quinazolinone‐Based Nitriles with Arylboronic Acids: Synthesis of 2‐(4‐Arylquinazolin‐2‐yl)anilines - Zhang - 2018 - Advanced Synthesis & Catalysis - Wiley Online Library
![Recent Advances in the Palladium Catalyzed Suzuki–Miyaura Cross-Coupling Reaction in Water | SpringerLink Recent Advances in the Palladium Catalyzed Suzuki–Miyaura Cross-Coupling Reaction in Water | SpringerLink](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs10562-016-1707-8/MediaObjects/10562_2016_1707_Sch16_HTML.gif)
Recent Advances in the Palladium Catalyzed Suzuki–Miyaura Cross-Coupling Reaction in Water | SpringerLink
![Post-transcriptional labeling by using Suzuki-Miyaura cross-coupling generates functional RNA probes. - Abstract - Europe PMC Post-transcriptional labeling by using Suzuki-Miyaura cross-coupling generates functional RNA probes. - Abstract - Europe PMC](https://europepmc.org/articles/PMC6009664/bin/gky185fig1.jpg)
Post-transcriptional labeling by using Suzuki-Miyaura cross-coupling generates functional RNA probes. - Abstract - Europe PMC
![A novel colorimetric and fluorescent probe for the highly selective and sensitive detection of palladium based on Pd(0) mediated reaction - Tetrahedron - X-MOL A novel colorimetric and fluorescent probe for the highly selective and sensitive detection of palladium based on Pd(0) mediated reaction - Tetrahedron - X-MOL](https://xpic.x-mol.com/thesis%2FTetrahedron%2F1-s2.0-S0040402015012132-fx1.jpg)
A novel colorimetric and fluorescent probe for the highly selective and sensitive detection of palladium based on Pd(0) mediated reaction - Tetrahedron - X-MOL
![Suzuki homo-coupling reaction based fluorescent sensors for monosaccharides - RSC Advances (RSC Publishing) DOI:10.1039/C4RA07331B Suzuki homo-coupling reaction based fluorescent sensors for monosaccharides - RSC Advances (RSC Publishing) DOI:10.1039/C4RA07331B](https://pubs.rsc.org/image/article/2014/RA/c4ra07331b/c4ra07331b-f1_hi-res.gif)
Suzuki homo-coupling reaction based fluorescent sensors for monosaccharides - RSC Advances (RSC Publishing) DOI:10.1039/C4RA07331B
![Palladium-catalyzed, direct boronic acid synthesis from aryl chlorides: a simplified route to diverse boronate ester derivatives.,Journal of the American Chemical Society - X-MOL Palladium-catalyzed, direct boronic acid synthesis from aryl chlorides: a simplified route to diverse boronate ester derivatives.,Journal of the American Chemical Society - X-MOL](https://xpic.x-mol.com/paperImg%2F2020_03_12%2FJournal_of_the_American_Chemical_Society_All_img%2F10.1021_ja1089759.gif)
Palladium-catalyzed, direct boronic acid synthesis from aryl chlorides: a simplified route to diverse boronate ester derivatives.,Journal of the American Chemical Society - X-MOL
![A simple and highly selective fluorescent sensor for palladium based on benzofuran-2-boronic acid - ScienceDirect A simple and highly selective fluorescent sensor for palladium based on benzofuran-2-boronic acid - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0040403917307141-fx1.jpg)
A simple and highly selective fluorescent sensor for palladium based on benzofuran-2-boronic acid - ScienceDirect
![meta-Selective C–H functionalisation of aryl boronic acids directed by a MIDA-derived boronate ester - Chem. Sci. - X-MOL meta-Selective C–H functionalisation of aryl boronic acids directed by a MIDA-derived boronate ester - Chem. Sci. - X-MOL](https://xpic.x-mol.com/20200326%2F10.1039_D0SC00230E.jpg)
meta-Selective C–H functionalisation of aryl boronic acids directed by a MIDA-derived boronate ester - Chem. Sci. - X-MOL
![Pd(NHC)-catalyzed alkylsulfonylation of boronic acids: a general and efficient approach for sulfone synthesis - Chem. Commun. - X-MOL Pd(NHC)-catalyzed alkylsulfonylation of boronic acids: a general and efficient approach for sulfone synthesis - Chem. Commun. - X-MOL](https://xpic.x-mol.com/20171117%2F10.1039_C7CC05851A.jpg)
Pd(NHC)-catalyzed alkylsulfonylation of boronic acids: a general and efficient approach for sulfone synthesis - Chem. Commun. - X-MOL
![A simple boronic acid-based fluorescent probe for selective detection of hydrogen peroxide in solutions and living cells - X-MOL A simple boronic acid-based fluorescent probe for selective detection of hydrogen peroxide in solutions and living cells - X-MOL](https://xpic.x-mol.com/20180909%2F10.1016_j.bioorg.2018.08.036.jpg)