| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5219456 | Tetrahedron | 2012 | 4 Pages |
Abstract
A concise synthesis of spirofuranopyrimidines is described and relies on the addition of isopropyl 4-oxopiperidine-1-carboxylate to a pyrimidine dianion. The diol intermediate formed is subjected to cycloetherification conditions leading to an unprecedented heterocyclic template.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Etzer Darout, Kim F. McClure, Vincent Mascitti,