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.
| Autors principals: | , , |
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| Format: | Journal article |
| Idioma: | English |
| Publicat: |
1998
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| Sumari: | 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. |
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