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.

Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς: Dixon, D, Ley, S, Tate, E
Μορφή: Journal article
Γλώσσα:English
Έκδοση: 1998
Περιγραφή
Περίληψη: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.