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.

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Hlavní autoři: Dixon, D, Ley, S, Tate, E
Médium: Journal article
Jazyk:English
Vydáno: 1998