| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5262318 | Tetrahedron Letters | 2015 | 5 Pages |
Abstract
The 1,3-dipolar cycloaddition of azomethine ylide generated in situ from isatin and proline to a series of (Z)-5-arylidene-3-(2-cyclopropyl-1-(2-fluorophenyl)-2-oxoethyl)-thiazolidine-2,4-diones led to the unprecedented formation of dispiro oxindole-pyrrolizine-thiazolidine-2,4-dione hybrids contrary to the commonly observed regiochemistry.
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Authors
Singanan Ponnuchamy, Remani Vasudevan Sumesh, Raju Ranjith Kumar,