| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5279822 | Tetrahedron Letters | 2006 | 6 Pages |
Abstract
The synthesis of novel polycyclic thiopyrano coumarin/chromone frameworks through intramolecular domino Knoevenagel hetero Diels-Alder reactions of 4-hydroxy coumarin and its benzo-analogous with S-prenylated aromatic aldehydes was studied. A high degree of chemoselectivity was achieved by the application of microwave irradiation and a solid support.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
![An efficient synthesis of thiopyrano[5,6-c]coumarin/[6,5-c]chromones through intramolecular domino Knoevenagel hetero Diels-Alder reactions](/preview/png/5279822.png "First Page Preview: An efficient synthesis of thiopyrano[5,6-c]coumarin/[6,5-c]chromones through intramolecular domino Knoevenagel hetero Diels-Alder reactions")
Authors
Jayadevan Jayashankaran, Rathna Durga R.S. Manian, Raghavachary Raghunathan,