| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5263215 | Tetrahedron Letters | 2013 | 5 Pages |
Abstract
A series of polysubstituted pyrano[3,2-f]quinoline and phenanthroline derivatives have been synthesized by molecular iodine-catalyzed tandem reaction of various propargylic alcohols with or without substituted amines in excellent yields. Moreover, the cyclized side products are also pyrano[3,2-f]quinoline and phenanthroline derivatives.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
K.C. Majumdar, Sudipta Ponra, Tapas Ghosh,
![First Page Preview: Regioselective synthesis of pyrano[3,2-f]quinoline and phenanthroline derivatives using molecular iodine Regioselective synthesis of pyrano[3,2-f]quinoline and phenanthroline derivatives using molecular iodine](/preview/png/5263215.png)