| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5291185 | Tetrahedron Letters | 2006 | 4 Pages |
Abstract
1,3-Dipolar cycloadditions of homochiral betaine 4 proceeded in moderate to good yields, with excellent diastereofacial selectivity achieved for the major 6-exo cycloadducts 7 and 11. The absolute stereochemistry of 7 was confirmed by a single-crystal X-ray diffraction study.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Neil R. Curtis, Richard G. Ball, Janusz J. Kulagowski,
![First Page Preview: 8-Azabicyclo[3.2.1]oct-3-en-2-ones via asymmetric 1,3-dipolar cycloaddition of a homochiral 3-oxidopyridinium betaine 8-Azabicyclo[3.2.1]oct-3-en-2-ones via asymmetric 1,3-dipolar cycloaddition of a homochiral 3-oxidopyridinium betaine](/preview/png/5291185.png)