| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5271351 | Tetrahedron Letters | 2014 | 4 Pages |
Abstract
A new three-component reaction of α-thiocyanato ketones under microwave irradiation for the stereoselective synthesis of 25 examples of E-3-aroylidene-2-oxindole derivatives has been described. The domino reaction simultaneously installs C–S and C–C bonds through continuous [3+2] cycloaddition/ring opening of in situ generated 1,3-oxathiolanes/SN2-type reaction sequence.
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