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ALKYNE-ACETAL CYCLISATION REACTIONS MEDIATED BY FORMIC ACID; 3-ACYLATED-2,5-DIHYDROFURANS AND RELATED OXYGEN AND NITROGEN HETEROCYCLES
Research output: Contribution to journal › Article › peer-review
Published copy (DOI)
Author(s)
Department/unit(s)
Publication details
| Journal | Heterocycles |
|---|---|
| Date | Published - 1 Jan 2012 |
| Issue number | 2 |
| Volume | 84 |
| Number of pages | 9 |
| Pages (from-to) | 1013-1021 |
| Original language | English |
Abstract
The utility of formic acid for the cyclisation of alkyne omega-acetals is described; the scope and limitations of this process are outlined and a range of acylated heterocyclic building blocks (2,5-dihydrofurans, 2,5-dihydro-1H-pyrroles, tetrahydropyridines, 2H-chromenes, 1,2-dihydroquinolines and benzoxepin5-(2H)-ones) are reported.
Projects
Triple Diels-Alder Cascades: Development and Application
Project: Research project (funded) › Research
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