| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5270781 | Tetrahedron Letters | 2013 | 4 Pages |
Abstract
Ornithine methyl ester reacts with aromatic aldehydes to generate bis-Schiff bases, which depending on the structure of the aromatic aldehyde, further undergo an intramolecular cycloaddition through the transient formation of a reactive 1,3-dipole.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
