Abstract
Annulation reactions based on oxetanes are important strategies for constructing heterocyclic compounds. In this paper, a Cu-catalyzed formal [4+2] annulation reaction between oxetan-3-ols and benzene-1,2-diols was developed, and a series of benzodioxane compounds were successfully synthesized. The activation of oxetan-3-ols with a trichloroacetimidate group was the key to the success of the reaction, which made the C–O bond of oxetan-3-ols easier to break. Under the copper catalyst, benzene-1,2-diols could efficiently undergo tandem nucleophilic attacking and ring-opening reactions with oxetan-3-ols for the synthesis of target benzodioxanes. In addition, the hydroxymethyl group reserved in the product was verified to have potential application value in synthetic transformations.
| Original language | English |
|---|---|
| Pages (from-to) | 11211-11216 |
| Number of pages | 6 |
| Journal | Organic Letters |
| Volume | 27 |
| Issue number | 40 |
| DOIs | |
| Publication status | Published - 26 Sept 2025 |
Bibliographical note
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