| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5222381 | Tetrahedron | 2011 | 5 Pages |
Abstract
A general method for the preparation of the MacMillan imidazolidinones is described. Treatment of an α-amino amide with a carbonyl compound in refluxing chloroform in the presence of Yb(OTf)3 (1 mol %) provides convenient access to the corresponding imidazolidinones.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Leopold Samulis, Nicholas C.O. Tomkinson,