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.

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون: Dixon, D, Ley, S, Tate, E
التنسيق: Journal article
اللغة:English
منشور في: 1998