| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1266515 | Ultrasonics Sonochemistry | 2008 | 5 Pages |
Abstract
An efficient and environmentally friendly procedure promoted by ultrasound irradiation is developed for stereoselective ring opening of various epoxides with aromatic and aliphatic amines under aqueous conditions in the presence of no catalyst or additive. Chemoselectivity of the protocol is shown by competition of piperidine and aniline to react with different epoxides resulting in exclusive formation of the respective products of piperidine.
Related Topics
Physical Sciences and Engineering
Chemistry
Chemistry (General)
Authors
M. Saeed Abaee, Vahid Hamidi, Mohammad M. Mojtahedi,