| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5219866 | Tetrahedron | 2012 | 9 Pages |
Abstract
A diastereoselective synthesis of helix-forming pseudopeptidic hydantoins by an Ugi 4CC/cyclization/reduction/Ugi 4CC sequence of reactions, giving mainly the l-adduct when benzoic acids were used, is described.
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