| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5264648 | Tetrahedron Letters | 2014 | 6 Pages |
Abstract
Efficient and facile synthesis of 7H-benzopyrano[3,2-c]coumarins has been achieved by mild base promoted reaction of 4-chloro-3-formylcoumarin with diversely functionalized resorcinols. All the products were obtained as pure precipitates from the reaction mixture and the structure of the product was confirmed by X-ray analysis.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Satyanarayana Reddy Jaggavarapu, Anand Solomon Kamalakaran, Jagadeesh Babu Nanubolu, Venkata Prasad Jalli, Sravan Kumar Gangisetty, Gopikrishna Gaddamanugu,
![First Page Preview: Synthesis of novel benzopyrano[3,2-c]coumarins via tandem base promoted nucleophilic substitution and intramolecular electrophilic aromatic cyclization Synthesis of novel benzopyrano[3,2-c]coumarins via tandem base promoted nucleophilic substitution and intramolecular electrophilic aromatic cyclization](/preview/png/5264648.png)