| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1347973 | Tetrahedron: Asymmetry | 2007 | 4 Pages |
Abstract
The synthesis of orthogonally protected 3-(aminomethyl)-2-(carboxymethyl)isoxazolidinyl thymine, a convenient monomer for the preparation of novel isoxazolidinyl peptide nucleic acid analogues, has been achieved through enantioselective 1,3-dipolar cycloaddition between N-glycosyl nitrones and vinyl acetate.
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Authors
Pedro Merino, Tomás Tejero, Juan Matés, Ugo Chiacchio, Antonino Corsaro, Giovanni Romeo,