Abstract
Boron trifluoride supported on hydroxyapatite nanorods efficiently catalyzed the ring opening reaction of α- epoxyketones in methanol solution to afford the corresponding α-hydroxy-β-methoxyketones through Cβ–O bond cleavage in excellent yields at room temperature. The type and position of the additional substituent affect not only the rate of ring opening but also the diastereomeric ratios products.
Keywords: Boron trifluoride, epoxyketones, hydroxyapatite, reusable, ring opening.
Letters in Organic Chemistry
Title:Hydroxyapatite Nanorods Supported Boron Trifluoride: An Efficient, Reusable and Eco-friendly Heterogeneous Catalyst for Ring Opening of α-Epoxyketones
Volume: 10 Issue: 9
Author(s): Ali Saffar-Teluri
Affiliation:
Keywords: Boron trifluoride, epoxyketones, hydroxyapatite, reusable, ring opening.
Abstract: Boron trifluoride supported on hydroxyapatite nanorods efficiently catalyzed the ring opening reaction of α- epoxyketones in methanol solution to afford the corresponding α-hydroxy-β-methoxyketones through Cβ–O bond cleavage in excellent yields at room temperature. The type and position of the additional substituent affect not only the rate of ring opening but also the diastereomeric ratios products.
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Cite this article as:
Saffar-Teluri Ali, Hydroxyapatite Nanorods Supported Boron Trifluoride: An Efficient, Reusable and Eco-friendly Heterogeneous Catalyst for Ring Opening of α-Epoxyketones, Letters in Organic Chemistry 2013; 10 (9) . https://dx.doi.org/10.2174/15701786113109990033
DOI https://dx.doi.org/10.2174/15701786113109990033 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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