Diastereoselective anomeric oxygen to carbon rearrangements of silyl enol ether derivatives of lactols.

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.

Dettagli Bibliografici
Autori principali:	Dixon, D, Ley, S, Tate, E
Natura:	Journal article
Lingua:	English
Pubblicazione:	1998

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