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YCl3-Catalyzed Highly Selective Ring Opening of Epoxides by Amines at Room Temperature and under Solvent-Free Conditions
oleh: Wuttichai Natongchai, Rais Ahmad Khan, Ali Alsalme, Rafik Rajjak Shaikh
Format: | Article |
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Diterbitkan: | MDPI AG 2017-11-01 |
Deskripsi
A simple, efficient, and environmentally benign approach for the synthesis of β-amino alcohols is herein described. YCl3 efficiently carried out the ring opening of epoxides by amines to produce β-amino alcohols under solvent-free conditions at room temperature. This catalytic approach is very effective, with several aromatic and aliphatic oxiranes and amines. A mere 1 mol % concentration of YCl3 is enough to deliver β-amino alcohols in good to excellent yields with high regioselectivity.