| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1348431 | Tetrahedron: Asymmetry | 2007 | 6 Pages |
Abstract
Chiral 1,3-substituted 1,2,3,4-tetrahydroisoquinolines have been synthesized in acceptable yield and diastereoselectivity through a three component reaction, starting from aromatic halides, enantiopure bromoalkyl derivatives and methyl acrylate, under palladium catalysis.
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Raffaella Ferraccioli, Clelia Giannini, Giorgio Molteni,