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Grignard-Type Arylation of Aldehydes via a Rhodium-Catalyzed CH Activation under Mild Conditions

✍ Scribed by Luo Yang; Camille A. Correia; Chao-Jun Li


Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
188 KB
Volume
353
Category
Article
ISSN
1615-4150

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✦ Synopsis


An efficient Grignard-type arylation of aldehydes via aryl C À H activation was achieved under mild conditions catalyzed by rhodium. The reaction provides an easy access to a wide variety of benzyl alcohols and can tolerate various functional groups as well as air and water.


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## Abstract An efficient oxidative cross‐coupling reaction between 1,3‐diarylpropenes and indoles in the presence of palladium chloride was achieved with 2,3‐dichloro‐5,6‐dicyanoquinone (DDQ) as oxidant. The reaction afforded 1,3‐diphenylallylindoles in moderate to high yields under mild conditions