Diastereoselective anomeric oxygen to carbon rearrangements of silyl enol ether derivatives of lactols.
Lewis acid promoted oxygen to carbon rearrangement of anomerically linked silyl enol ethers gives a new and diastereoselective route to the corresponding 2-α-hydroxyketone substituted products.
मुख्य लेखकों: | Dixon, D, Ley, S, Tate, E |
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स्वरूप: | Journal article |
भाषा: | English |
प्रकाशित: |
1998
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समान संसाधन
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प्रकाशित: (2004) -
A general C-glycosidation procedure via anomeric oxygen to carbon rearrangements of tetrahydropyranyl ether derivatives
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