Title of article
Palladium-catalyzed reaction of aryl iodides with tertiary propargylic amides.: Highly substituted allenes through a regioselective carbopalladation/β-NPd elimination reaction
Author/Authors
Antonio Arcadi، نويسنده , , Sandro Cacchi، نويسنده , , Giancarlo Fabrizi، نويسنده , , Fabio Marinelli، نويسنده , , Luca M Parisi، نويسنده ,
Issue Information
دوفصلنامه با شماره پیاپی سال 2003
Pages
5
From page
562
To page
566
Abstract
The palladium-catalyzed reaction of aryl iodides with tertiary propargylic amides affords highly substituted allenes. Best results have been obtained by using Pd(OAc)2, nBu3N, HCOOH, and nBu4NCl or LiCl in DME at 100 °C. The reaction is highly regioselective and the carbopalladation step is controlled by the strong directing effect of the tertiary amide group.
Keywords
Palladium , Allenes , hydroarylation , alkynes
Journal title
Journal of Organometallic Chemistry
Serial Year
2003
Journal title
Journal of Organometallic Chemistry
Record number
1376563
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