![New trends and applications in cyanation isotope chemistry - Derdau - 2018 - Journal of Labelled Compounds and Radiopharmaceuticals - Wiley Online Library New trends and applications in cyanation isotope chemistry - Derdau - 2018 - Journal of Labelled Compounds and Radiopharmaceuticals - Wiley Online Library](https://analyticalsciencejournals.onlinelibrary.wiley.com/cms/asset/d0843014-ac44-4fd9-b45d-e33212937f23/jlcr3630-fig-0009-m.jpg)
New trends and applications in cyanation isotope chemistry - Derdau - 2018 - Journal of Labelled Compounds and Radiopharmaceuticals - Wiley Online Library
![Recent advances and prospects in the palladium-catalyzed cyanation of aryl halides - RSC Advances (RSC Publishing) DOI:10.1039/D0RA05960A Recent advances and prospects in the palladium-catalyzed cyanation of aryl halides - RSC Advances (RSC Publishing) DOI:10.1039/D0RA05960A](https://pubs.rsc.org/image/article/2020/RA/d0ra05960a/d0ra05960a-s37_hi-res.gif)
Recent advances and prospects in the palladium-catalyzed cyanation of aryl halides - RSC Advances (RSC Publishing) DOI:10.1039/D0RA05960A
![An overview of microwave assisted cyanation reactions - Fairoosa - 2021 - Applied Organometallic Chemistry - Wiley Online Library An overview of microwave assisted cyanation reactions - Fairoosa - 2021 - Applied Organometallic Chemistry - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/688a1009-7f45-4135-aceb-38e2c7221857/aoc6356-fig-0006-m.jpg)
An overview of microwave assisted cyanation reactions - Fairoosa - 2021 - Applied Organometallic Chemistry - Wiley Online Library
![Controllable cyanation of carbon-hydrogen bonds by zeolite crystals over manganese oxide catalyst | Nature Communications Controllable cyanation of carbon-hydrogen bonds by zeolite crystals over manganese oxide catalyst | Nature Communications](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fncomms15240/MediaObjects/41467_2017_Article_BFncomms15240_Fig1_HTML.jpg)
Controllable cyanation of carbon-hydrogen bonds by zeolite crystals over manganese oxide catalyst | Nature Communications
![New trends and applications in cyanation isotope chemistry - Derdau - 2018 - Journal of Labelled Compounds and Radiopharmaceuticals - Wiley Online Library New trends and applications in cyanation isotope chemistry - Derdau - 2018 - Journal of Labelled Compounds and Radiopharmaceuticals - Wiley Online Library](https://analyticalsciencejournals.onlinelibrary.wiley.com/cms/asset/262e4955-d5ec-4543-adc4-ec3257af4629/jlcr3630-fig-0025-m.jpg)
New trends and applications in cyanation isotope chemistry - Derdau - 2018 - Journal of Labelled Compounds and Radiopharmaceuticals - Wiley Online Library
![A mild and efficient palladium-catalyzed cyanation of aryl chlorides with K4[Fe(CN)6]. | Semantic Scholar A mild and efficient palladium-catalyzed cyanation of aryl chlorides with K4[Fe(CN)6]. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/861f9c3deb3dc91f7afcf7091bed27b2ed59c45c/2-Figure1-1.png)
A mild and efficient palladium-catalyzed cyanation of aryl chlorides with K4[Fe(CN)6]. | Semantic Scholar
![PDF) ChemInform Abstract: Synthesis of Phthalonitriles Using a Palladium Catalyst | zafar Iqbal - Academia.edu PDF) ChemInform Abstract: Synthesis of Phthalonitriles Using a Palladium Catalyst | zafar Iqbal - Academia.edu](https://0.academia-photos.com/attachment_thumbnails/52644849/mini_magick20190122-25333-1v9pggt.png?1548202069)
PDF) ChemInform Abstract: Synthesis of Phthalonitriles Using a Palladium Catalyst | zafar Iqbal - Academia.edu
![Catalysts | Free Full-Text | Solid-Supported Palladium Catalysts in Sonogashira Reactions: Recent Developments | HTML Catalysts | Free Full-Text | Solid-Supported Palladium Catalysts in Sonogashira Reactions: Recent Developments | HTML](https://www.mdpi.com/catalysts/catalysts-08-00202/article_deploy/html/images/catalysts-08-00202-g015.png)
Catalysts | Free Full-Text | Solid-Supported Palladium Catalysts in Sonogashira Reactions: Recent Developments | HTML
![A General, Practical Palladium‐Catalyzed Cyanation of (Hetero)Aryl Chlorides and Bromides - Senecal - 2013 - Angewandte Chemie International Edition - Wiley Online Library A General, Practical Palladium‐Catalyzed Cyanation of (Hetero)Aryl Chlorides and Bromides - Senecal - 2013 - Angewandte Chemie International Edition - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/1cd8eaaf-ebfa-4965-82d5-03d7a9513e19/mcontent.jpg)
A General, Practical Palladium‐Catalyzed Cyanation of (Hetero)Aryl Chlorides and Bromides - Senecal - 2013 - Angewandte Chemie International Edition - Wiley Online Library
![General and Mild Nickel-Catalyzed Cyanation of Aryl/Heteroaryl Chlorides with Zn(CN)2: Key Roles of DMAP. | Semantic Scholar General and Mild Nickel-Catalyzed Cyanation of Aryl/Heteroaryl Chlorides with Zn(CN)2: Key Roles of DMAP. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/694765de0330b885e7a7ddb72042f5b0ea1499bb/2-Table1-1.png)
General and Mild Nickel-Catalyzed Cyanation of Aryl/Heteroaryl Chlorides with Zn(CN)2: Key Roles of DMAP. | Semantic Scholar
![Microwave-enhanced cyanation of aryl halides with a dimeric ortho-palladated complex catalyst | SpringerLink Microwave-enhanced cyanation of aryl halides with a dimeric ortho-palladated complex catalyst | SpringerLink](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs11243-011-9525-8/MediaObjects/11243_2011_9525_Sch3_HTML.gif)
Microwave-enhanced cyanation of aryl halides with a dimeric ortho-palladated complex catalyst | SpringerLink
![C–CN bond formation: an overview of diverse strategies - Chemical Communications (RSC Publishing) DOI:10.1039/D0CC07783F C–CN bond formation: an overview of diverse strategies - Chemical Communications (RSC Publishing) DOI:10.1039/D0CC07783F](https://pubs.rsc.org/image/article/2021/CC/d0cc07783f/d0cc07783f-s6_hi-res.gif)
C–CN bond formation: an overview of diverse strategies - Chemical Communications (RSC Publishing) DOI:10.1039/D0CC07783F
![A general, practical palladium-catalyzed cyanation of (hetero)aryl chlorides and bromides. | Semantic Scholar A general, practical palladium-catalyzed cyanation of (hetero)aryl chlorides and bromides. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/f1e4f4046f199a5a4f85667494db048a55bb3c4b/11-Table1-1.png)
A general, practical palladium-catalyzed cyanation of (hetero)aryl chlorides and bromides. | Semantic Scholar
![Catalysts | Free Full-Text | Microwave-Assisted Palladium-Catalyzed Cross-Coupling Reactions: Generation of Carbon–Carbon Bond | HTML Catalysts | Free Full-Text | Microwave-Assisted Palladium-Catalyzed Cross-Coupling Reactions: Generation of Carbon–Carbon Bond | HTML](https://www.mdpi.com/catalysts/catalysts-10-00004/article_deploy/html/images/catalysts-10-00004-sch007.png)