Abstract
A regioselective synthesis of furanone-fused isoquinoline heterocycles is developed in a single step using a Rh(III) catalyst. In this reaction, a cascade C–H activation, regioselective annulation, and lactonization occur in one pot. A wide range of alkynoates was examined, which showed good regioselectivity. The regioselectivity was guided by steric bulk at the C4 position of the 4-hydroxy-2-alkynoates. The synthetic utility was exemplified, and the model reaction was scaled up to a 1 g scale.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 17965-17974 |
| Number of pages | 10 |
| Journal | Journal of Organic Chemistry |
| Volume | 86 |
| Issue number | 24 |
| DOIs | |
| State | Published - Dec 17 2021 |
| Externally published | Yes |
ASJC Scopus subject areas
- Organic Chemistry
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