Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1324089 | Journal of Organometallic Chemistry | 2005 | 9 Pages |
The Sonogashira coupling reaction of aryl halides with a masked acetylene, leading to the formation of diarylethynes is reviewed. The process is either run in a sequential coupling–deprotection–coupling manner, or sometimes it is carried out in one-pot, a reaction we coined domino coupling. The procedures were also extended to the synthesis of compound libraries.
Graphical abstractThe Sonogashira coupling reaction of aryl halides with a masked acetylene, leading to the formation of diarylethynes is reviewed. The process is either run in a sequential coupling–deprotection–coupling manner, or sometimes it is carried out in one-pot, a reaction we coined domino coupling. The procedures were also extended to the synthesis of compound libraries.Figure optionsDownload full-size imageDownload as PowerPoint slide