Baylis-Hillman acetates in organic synthesis: A simple two-step strategy for oxindole-spiro-α-arylidene-γ-butyrolactone framework
Baylis-Hillman acetates in organic synthesis: A simple two-step strategy for oxindole-spiro-α-arylidene-γ-butyrolactone framework
| dc.contributor.author | Basavaiah, Deevi | |
| dc.contributor.author | Lingam, Harathi | |
| dc.contributor.author | Babu, Thelagathoti Hari | |
| dc.date.accessioned | 2022-03-27T09:00:41Z | |
| dc.date.available | 2022-03-27T09:00:41Z | |
| dc.date.issued | 2018-05-10 | |
| dc.description.abstract | A facile, convenient, and two step strategy for synthesis of spirooxindoles containing α-arylidene-γ-butyrolactone moiety has been developed via monoalkylation of 2-oxindoles with Baylis-Hillman acetates followed by the spirolactonization of the resulting cinnamic esters on treatment with phenyliodine (III) bistrifluoroacetate (PIFA). | |
| dc.identifier.citation | Tetrahedron. v.74(19) | |
| dc.identifier.issn | 00404020 | |
| dc.identifier.uri | 10.1016/j.tet.2018.03.035 | |
| dc.identifier.uri | https://www.sciencedirect.com/science/article/abs/pii/S0040402018302783 | |
| dc.identifier.uri | https://dspace.uohyd.ac.in/handle/1/12261 | |
| dc.subject | Baylis-Hillman reaction | |
| dc.subject | PIFA | |
| dc.subject | Spirolactonization | |
| dc.subject | Spirooxindole | |
| dc.subject | γ-Butyrolactone | |
| dc.title | Baylis-Hillman acetates in organic synthesis: A simple two-step strategy for oxindole-spiro-α-arylidene-γ-butyrolactone framework | |
| dc.type | Journal. Article | |
| dspace.entity.type |
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