Synthesis of diaryl ethers through the copper-promoted arylation of phenols with arylboronic acids. An expedient synthesis of thyroxine
β Scribed by David A Evans; Jeffrey L Katz; Theodore R West
- Book ID
- 104259155
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 287 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
Diaryl ethers are readily synthesized in high yield at room temperature through the copper(II)-prorooted coupling of arylboronic acids and phenols. The reaction is tolerant of a wide range of substituents on both coupling partners. These reaction conditions permit the racemization-free arylation of phenolic amino acids, methodology that has been applied to an efficient synthesis of thyroxine.
π SIMILAR VOLUMES
The copper-catalyzed arylation of phenols with a variety of aryl halides using microwave heating is described.
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v