Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5272795 | Tetrahedron Letters | 2013 | 11 Pages |
Abstract
Ethyl lactate as a bio based green solvent was used, for the first time to promote the 1,3-dipolar cycloaddition reaction of azomethine ylide generated in situ by the decarboxylative condensation of substituted isatin and proline with napthoquinone as dipolarophile, which generates a series of medicinally privileged spiro[benzo[f]pyrrolo[2,1-a]isoindole-5,3â²-indoline]-2â²,6,11-trione derivatives in excellent yields at room temperature.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Anshu Dandia, Anuj K. Jain, Ashok K. Laxkar,