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.

Chi tiết về thư mục
Những tác giả chính: Dixon, D, Ley, S, Tate, E
Định dạng: Journal article
Ngôn ngữ:English
Được phát hành: 1998
Miêu tả
Tóm tắt: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.