![Application of Chan-Lam cross coupling for the synthesis of N-heterocyclic carbene precursors bearing strong electron donating or withdrawing groups | Scientific Reports Application of Chan-Lam cross coupling for the synthesis of N-heterocyclic carbene precursors bearing strong electron donating or withdrawing groups | Scientific Reports](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fsrep12431/MediaObjects/41598_2015_Article_BFsrep12431_Fig2_HTML.jpg)
Application of Chan-Lam cross coupling for the synthesis of N-heterocyclic carbene precursors bearing strong electron donating or withdrawing groups | Scientific Reports
![A room temperature one-pot Knoevenagel-Chan-Evans-Lam coupling reaction for synthesis of N-aryl-2-Iminocoumarins in bio-mass-derived green solvent 2-methylTHF - ScienceDirect A room temperature one-pot Knoevenagel-Chan-Evans-Lam coupling reaction for synthesis of N-aryl-2-Iminocoumarins in bio-mass-derived green solvent 2-methylTHF - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0040403919306926-gr7.jpg)
A room temperature one-pot Knoevenagel-Chan-Evans-Lam coupling reaction for synthesis of N-aryl-2-Iminocoumarins in bio-mass-derived green solvent 2-methylTHF - ScienceDirect
![Visible‐Light‐Mediated Chan–Lam Coupling Reactions of Aryl Boronic Acids and Aniline Derivatives - Yoo - 2015 - Angewandte Chemie International Edition - Wiley Online Library Visible‐Light‐Mediated Chan–Lam Coupling Reactions of Aryl Boronic Acids and Aniline Derivatives - Yoo - 2015 - Angewandte Chemie International Edition - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/6d2d9d1f-c092-4426-bf17-fc745b88afeb/msch001.jpg)
Visible‐Light‐Mediated Chan–Lam Coupling Reactions of Aryl Boronic Acids and Aniline Derivatives - Yoo - 2015 - Angewandte Chemie International Edition - Wiley Online Library
![A Review on the Latest Progress of Chan‐Lam Coupling Reaction - Chen - 2020 - Advanced Synthesis & Catalysis - Wiley Online Library A Review on the Latest Progress of Chan‐Lam Coupling Reaction - Chen - 2020 - Advanced Synthesis & Catalysis - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/4e557460-b903-41a1-bce5-4283e30c645d/adsc202000495-gra-0025.png)
A Review on the Latest Progress of Chan‐Lam Coupling Reaction - Chen - 2020 - Advanced Synthesis & Catalysis - Wiley Online Library
![Autocatalytic photoredox Chan-Lam coupling of free diaryl sulfoximines with arylboronic acids | Nature Communications Autocatalytic photoredox Chan-Lam coupling of free diaryl sulfoximines with arylboronic acids | Nature Communications](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fs41467-021-21156-w/MediaObjects/41467_2021_21156_Fig1_HTML.png)
Autocatalytic photoredox Chan-Lam coupling of free diaryl sulfoximines with arylboronic acids | Nature Communications
![A Review on the Latest Progress of Chan‐Lam Coupling Reaction - Chen - 2020 - Advanced Synthesis & Catalysis - Wiley Online Library A Review on the Latest Progress of Chan‐Lam Coupling Reaction - Chen - 2020 - Advanced Synthesis & Catalysis - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/8008f887-3312-43cf-81f8-2fe15eea6e14/adsc202000495-fig-5002-m.png)
A Review on the Latest Progress of Chan‐Lam Coupling Reaction - Chen - 2020 - Advanced Synthesis & Catalysis - Wiley Online Library
![Advances in Cu and Ni-catalyzed Chan–Lam-type coupling: synthesis of diarylchalcogenides, Ar 2 –X (X = S, Se, Te) - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/D0OB02035D Advances in Cu and Ni-catalyzed Chan–Lam-type coupling: synthesis of diarylchalcogenides, Ar 2 –X (X = S, Se, Te) - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/D0OB02035D](https://pubs.rsc.org/image/article/2020/OB/d0ob02035d/d0ob02035d-f3_hi-res.gif)
Advances in Cu and Ni-catalyzed Chan–Lam-type coupling: synthesis of diarylchalcogenides, Ar 2 –X (X = S, Se, Te) - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/D0OB02035D
![Oxidative cross-coupling processes inspired by the Chan–Lam reaction - Chemical Communications (RSC Publishing) DOI:10.1039/D1CC00213A Oxidative cross-coupling processes inspired by the Chan–Lam reaction - Chemical Communications (RSC Publishing) DOI:10.1039/D1CC00213A](https://pubs.rsc.org/image/article/2021/CC/d1cc00213a/d1cc00213a-f1_hi-res.gif)
Oxidative cross-coupling processes inspired by the Chan–Lam reaction - Chemical Communications (RSC Publishing) DOI:10.1039/D1CC00213A
Chemoselective Chan–Lam Coupling Reactions between Benzimidazoline-2-thiones and Arylboronic Acids | The Journal of Organic Chemistry
![Spectroscopic Studies of the Chan–Lam Amination: A Mechanism-Inspired Solution to Boronic Ester Reactivity | Journal of the American Chemical Society Spectroscopic Studies of the Chan–Lam Amination: A Mechanism-Inspired Solution to Boronic Ester Reactivity | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/jacs.6b12800/asset/images/medium/ja-2016-128008_0023.gif)
Spectroscopic Studies of the Chan–Lam Amination: A Mechanism-Inspired Solution to Boronic Ester Reactivity | Journal of the American Chemical Society
![A Review on the Latest Progress of Chan‐Lam Coupling Reaction - Chen - 2020 - Advanced Synthesis & Catalysis - Wiley Online Library A Review on the Latest Progress of Chan‐Lam Coupling Reaction - Chen - 2020 - Advanced Synthesis & Catalysis - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/5dd047bd-8f5d-4beb-a53b-60b12caaa7a3/adsc202000495-fig-5001-m.png)