| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5279054 | Tetrahedron Letters | 2005 | 4 Pages |
Abstract
High regio- and diastereoselective ring opening of limonene aziridines with a variety of nucleophiles is described. The resulting novel chiral derivatives are readily accessible from limonene aziridine in either enantiomeric form in 35-94% yield.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Michael V. Voronkov, Ramanaiah C. Kanamarlapudi, Paul Richardson,