| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5218316 | Tetrahedron | 2013 | 7 Pages |
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.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
