Basavaiah, Deevi ; Badsara, Satpal Singh ; Veeraraghavaiah, Gorre (2013) Baylis–Hillman carbonates in organic synthesis: a convenient one-pot strategy for nitrone–spiro-oxindole frameworks Tetrahedron, 69 (37). pp. 7995-8001. ISSN 0040-4020
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Official URL: http://doi.org/10.1016/j.tet.2013.07.002
Related URL: http://dx.doi.org/10.1016/j.tet.2013.07.002
Abstract
A facile one-pot protocol for synthesis of nitrone–spiro-oxindole frameworks via alkylation of nitromethane with carbonates of Baylis–Hillman alcohols, derived from isatins and cyclohex-2-enone derivatives, followed by reductive cyclization is described.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Elsevier B.V. |
| ID Code: | 130113 |
| Deposited On: | 05 Dec 2022 05:54 |
| Last Modified: | 05 Dec 2022 05:54 |
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