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Cooper, DA, Robbins, E, Tizzard, GJ, Coles, SJ and O'Brien, M (2017) Furanyl Cyclic Ethers: Single and Double Diastereoselectivity in the Synthesis of 2,4-Di and 2,4,5-Trisubstituted Tetrahydropyrans. Journal Of Organic Chemistry, 82 (7). pp. 3441-3455. ISSN 0022-3263
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M OBrien - Furanyl Cyclic Ethers - Single and Double....pdf - Accepted Version
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Official URL: http://pubs.acs.org/doi/abs/10.1021/acs.joc.6b0283...
Abstract
Combining the desymmetrization of a prochiral bis-hydroxymethyl group with the epimerization of a chiral furanyl ether in a single transformation, high levels of double diastereoselectivity have been achieved in a synthesis of 2,4,5-trisubstituted tetrahydropyrans, which proceeds under thermodynamic control.
Item Type: | Article |
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Subjects: | Q Science > QD Chemistry |
Divisions: | Faculty of Natural Sciences > School of Chemical and Physical Sciences |
Related URLs: | |
Depositing User: | Symplectic |
Date Deposited: | 11 Apr 2017 15:19 |
Last Modified: | 28 Feb 2018 01:30 |
URI: | https://eprints.keele.ac.uk/id/eprint/3210 |
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