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Scandium triflate as an efficient and useful catalyst for the synthesis of β-amino alcohols by regioselective ring opening of epoxides with amines under solvent-free conditions
A simple and efficient method has been developed for the synthesis of β-amino alcohols by ring opening of epoxides in the presence of a catalytic amount of Sc(OTf) 3 at room temperature under solvent-free conditions. The reaction works well with both aromatic and aliphatic amines. High regio-, and d...
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Published in: | Tetrahedron letters 2005-12, Vol.46 (52), p.9029-9034 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | A simple and efficient method has been developed for the synthesis of β-amino alcohols by ring opening of epoxides in the presence of a catalytic amount of Sc(OTf)
3 at room temperature under solvent-free conditions. The reaction works well with both aromatic and aliphatic amines. High regio-, and diastereoselectivity can be considered as a noteworthy advantage of this method. |
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ISSN: | 0040-4039 1873-3581 |
DOI: | 10.1016/j.tetlet.2005.10.106 |