Abstract
A divergent synthesis of 1-aminonaphthalenes by the Diels–Alder reaction of 3-aminoarynes followed by diversification is disclosed. The cycloaddition of 3-aminoarynes with 2-substituted furans exhibits unusual proximal selectivity. Owing to the significant versatility of the resulting tricyclic ethers, a wide variety of highly functionalized 1-aminonaphthalenes can be prepared, thereby enabling rapid development of fluorescent dyes.
| Original language | English |
|---|---|
| Pages (from-to) | 3744-3750 |
| Number of pages | 7 |
| Journal | Journal of Organic Chemistry |
| Volume | 91 |
| Issue number | 10 |
| DOIs | |
| Publication status | Published - 13 Mar 2026 |
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