Synthesis of 1,4-Diarylbuta-1,3-dienes through Palladium- Catalyzed Decarboxylative Coupling of Unsaturated Carboxylic Acids
β Scribed by Mana Yamashita; Koji Hirano; Tetsuya Satoh; Masahiro Miura
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 228 KB
- Volume
- 353
- Category
- Article
- ISSN
- 1615-4150
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β¦ Synopsis
Abstract
It has been found that readily available hydroxylated cinnamic acids such as ferulic acid undergo palladiumβcatalyzed decarboxylative coupling with aryl iodides and internal alkynes in a 1:1:1 manner to produce 1,4βdiarylbutaβ1,3βdienes. The butadiene synthesis has also been achieved through the coupling of aryl halides with dienoic acids. Some of the products exhibit solidβstate fluorescence.
π SIMILAR VOLUMES
A cationic palladium complex, [Pd(PPh 3 ) 2 (MeCN) 2 ](BF 4 ) 2 , catalyzed the carbonylation of 2,3-dien-1-ols under mild conditions. The dienols bearing two or more alkyl substituents on the diene part afforded 1,3diene-2-carboxylic acids successfully in tetrahydrofuran (THF), while those possessi
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