| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5215362 | Tetrahedron | 2015 | 4 Pages |
Abstract
2-naphthol derivatives of resorcinarenes were synthesized by solvent-free 1,4 Michael addition reactions in yields up to 76%. This result is significantly better than in case of reactions in solution. Based on experimental results and previously known similar reactions a mechanism is proposed involving an in situ generated o-quino methide derivative of resorcinarene.
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