A highly active catalyst system for the heteroarylation of acetone
P Liu, TJ Lanza, JP Jewell, CP Jones, WK Hagmann…
Index: Liu, Ping; Lanza Jr., Thomas J.; Jewell, James P.; Jones, Carrie P.; Hagmann, William K.; Lin, Linus S. Tetrahedron Letters, 2003 , vol. 44, # 49 p. 8869 - 8871
Full Text: HTML
Citation Number: 28
Abstract
A highly active catalyst system for the heteroarylation of acetone has been identified. The coupling between the in situ generated tributyltin enolate of acetone and a variety of heteroaromatic bromides, chlorides, and triflates in the presence of this catalyst system provided arylacetones in good yields.
Related Articles:
[Amatore, Christian; Oturan, Mehmet A.; Pinson, Jean; Saveant, Jean-Michel; Thiebault, Andre Journal of the American Chemical Society, 1985 , vol. 107, p. 3451 - 3459]
Acétonylation Aromatique Homolytique
[Gardrat, C. Bulletin des Societes Chimiques Belges, 1984 , vol. 93, # 10 p. 897 - 902]
Acétonylation Aromatique Homolytique
[Gardrat, C. Bulletin des Societes Chimiques Belges, 1984 , vol. 93, # 10 p. 897 - 902]
Acétonylation Aromatique Homolytique
[Gardrat, C. Bulletin des Societes Chimiques Belges, 1984 , vol. 93, # 10 p. 897 - 902]