| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5218554 | Tetrahedron | 2013 | 6 Pages |
Abstract
The cyclization of fluoroalkylated 3,5-dioxoesters with hydrazines, carried out in glacial acetic acid, afforded pyrazines with fluoroalkylated side-chain. The cyclization of 3,5-dioxoesters with hydroxylamine afforded hydroxylated fluoroalkylated dihydroisoxazoles. All reactions proceeded with good to very good regioselectivity.
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