| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5278800 | Tetrahedron Letters | 2006 | 4 Pages |
Abstract
Reductive amination of homochiral primary amines ((R)- or (S)-α-methylbenzylamine, and (R)- or (S)-alanine methyl ester) with a racemic proline derived aldehyde, followed by cyclisation, gave diastereoisomeric [4.4]-spirolactams.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
![Spirobicyclic diamines. Part 2: Synthesis of homochiral diastereoisomeric proline derived [4.4]-spirolactams](/preview/png/5278800.png "First Page Preview: Spirobicyclic diamines. Part 2: Synthesis of homochiral diastereoisomeric proline derived [4.4]-spirolactams")
Authors
Fintan Kelleher, Sinead Kelly,