| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5265702 | Tetrahedron Letters | 2013 | 4 Pages |
Abstract
A novel, domino, multi-component reaction for the synthesis of polyfunctionalized spiro[benzo[c]pyrano[3,2-a]phenazine] derivatives has been established. l-Proline has been used as a bifunctional catalyst for the one-pot condensation of 2-hydroxy-1,4-naphthoquinone with aromatic 1,2-diamines to form the corresponding quinoxalines and then cyclo-condensation with an alkylmalonate and a cyclic carbonyl compound leads to novel spiro[benzo[c]pyrano[3,2-a]phenazine] derivatives in high yields and short reaction times.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Alireza Hasaninejad, Somayeh Firoozi, Fatemeh Mandegani,
![First Page Preview: An efficient synthesis of novel spiro[benzo[c]pyrano[3,2-a]phenazines] via domino multi-component reactions using l-proline as a bifunctional organocatalyst An efficient synthesis of novel spiro[benzo[c]pyrano[3,2-a]phenazines] via domino multi-component reactions using l-proline as a bifunctional organocatalyst](/preview/png/5265702.png)