| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5270235 | Tetrahedron Letters | 2010 | 4 Pages |
Abstract
A novel series of 5H-chromeno[2,3-c]acridine derivatives has been prepared through the intramolecular aza-Diels-Alder reaction of alkene-tethered chromene-3-carboxaldehyde with various aromatic amines. This is the first example of the preparation of pentacyclic poly aromatic compounds in a single-step operation at ambient temperature.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
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Authors
B.V. Subba Reddy, Aneesh Antony, J.S. Yadav,