Boron Trifluoride Etherate Induced Stille Cross-Coupling Reaction of Aryltriazenes with Tributyl(phenyl)stannane Catalyzed by Recyclable Pd/C Catalyst
Corresponding Author(s) : G.M. Nan1
Asian Journal of Chemistry,
Vol. 25 No. 18 (2013)
Abstract
A novel and efficient Pd/C-catalyzed Stille cross-coupling reaction of aryltriazenes with tributyl(phenyl)stannane has been realized in the presence of 1 equiv of BF3·OEt2 under room temperature. The Pd/C catalyst could be re-used several times and still retained its high activity. The present protocol, utilizes simple and recyclable catalyst, readily available starting materials and mild reaction conditions, provides an attractive methodology to a diverse range of biaryl products in moderate to excellent yields.
Keywords
Pd/C Catalyst
Stille cross-coupling
Aryltriazenes
Tributyl(phenyl)stannane
Boron trifluoride etherate
Recyclability.
Nan1, G., Zhou2, J., & Yan1, W. (2013). Boron Trifluoride Etherate Induced Stille Cross-Coupling Reaction of Aryltriazenes with Tributyl(phenyl)stannane Catalyzed by Recyclable Pd/C Catalyst. Asian Journal of Chemistry, 25(18), 10322–10324. https://doi.org/10.14233/ajchem.2013.15291
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