Facile synthesis of 3-arylpyrroles by tandem Suzuki–dehydrogenation reaction
✍ Scribed by Chi-Wan Lee; Yong Jun Chung
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- French
- Weight
- 86 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Facile method for the synthesis of 3-arylpyrroles is described based on the palladium-catalyzed coupling of trifluoromethanesulfonic acid 1-benzyl-2,5-dihydro-1H-pyrrol-3-yl ester with aryl halides.
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Glycosyl azides, prepared in situ from glucal and trimethylsilyl azide via Ferrier rearrangement, undergo smooth coupling with alkynes under neutral conditions by means of 'Click reactions' to furnish 1,2,3-triazole-linked glycoconjugates in high yields and with moderate stereoselectivity. The metho
## Abstract magnified image The synthesis of new 3‐substituted coumarins appended to imidazolium, pyridinium, 3‐dimethylamino pyridinium, 3‐chloro pyridinium and 3‐bromo pyridinium salts is reported. These salts were prepared by tandem reactions, followed by quantitative anionic metathesis. The st