| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 68251 | Journal of Molecular Catalysis A: Chemical | 2007 | 5 Pages |
Abstract
A variety of β-hydroxy nitriles and β-amino alcohols have been synthesized by the regioselective ring opening of epoxides and aziridines under neutral and aqueous conditions in the presence of β-cyclodextrin in good yields.
Graphical abstractVarious of β-hydroxy nitriles and β-amino alcohols have been synthesized regioselectively from epoxides and N-tosyl aziridines in the presence of β-cyclodextrin in good yields. Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Catalysis
Authors
B. Srinivas, V. Pavan Kumar, R. Sridhar, K. Surendra, Y.V.D. Nageswar, K. Rama Rao,