| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5275571 | Tetrahedron Letters | 2012 | 5 Pages |
Abstract
A highly efficient and regioselective Friedländer reaction of unsymmetrical 1,3-diketones with 2-aminoaryl aldehydes (ketones) is described. The methodology leads to the synthesis of a broad scope of substituted quinolines in high yield and excellent regioselectivity.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Ying Chen, Jinkun Huang, Tsang-Lin Hwang, T.J. Li, Sheng Cui, Johann Chan, Matthew Bio,