Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5267791 | Tetrahedron Letters | 2015 | 4 Pages |
Abstract
The synthesis of highly substituted quinolines was accomplished through a Heck reaction of substituted iodoanilines with Morita-Baylis-Hillman (MBH) adducts employing Nájera N-oxime derived palladacycle as catalyst. The reaction is completely regioselective and gives the products with good to excellent yields (up to 89%) with low catalyst loading and TONs of up to 89.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Lucas A. Zeoly, Rosimeire C. Barcelos, Manoel T. Jr., Ralph C. Gomes, Fernando Coelho,