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.

Manylion Llyfryddiaeth
Prif Awduron:	Dixon, D, Ley, S, Tate, E
Fformat:	Journal article
Iaith:	English
Cyhoeddwyd:	1998

Eitemau Tebyg

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