| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5218471 | Tetrahedron | 2013 | 7 Pages |
Abstract
The ring-opening reaction of 2-trifluoromethyl-N-tosylaziridine with a variety of heteroatom- and carbon-centered nucleophiles was achieved under basic conditions in good to high yield with excellent regioselectivity. These findings enabled an easy access to useful α-trifluoromethyl-N-tosylmethylamine derivatives, such as 1,2-aminoalcohol, 1,2-diamine, 1,2-aminothiol, and distant secondary amine.
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