Publication | Closed Access
Enantioselective Reaction of 2<i>H</i>-Azirines with Oxazol-5-(4<i>H</i>)-ones Catalyzed by Cinchona Alkaloid Sulfonamide Catalysts
27
Citations
59
References
2021
Year
The enantioselective reaction of 2<i>H</i>-azirines with oxazol-5-(4<i>H</i>)-ones (oxazolones) using a cinchona alkaloid sulfonamide catalyst has been developed. The reaction proceeded at the C-2 position of oxazolones to afford products with consecutive tetrasubstituted stereogenic centers in high yield with high diastereo- and enantioselectivity. The obtained aziridines were converted into various chiral compounds without loss of enantiopurity.
| Year | Citations | |
|---|---|---|
Page 1
Page 1