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Synthesis of diaryl ethers through the copper-promoted arylation of phenols with arylboronic acids. An expedient synthesis of thyroxine

✍ 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

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✦ 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.


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ChemInform Abstract: Synthesis of Diaryl
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