Harris Jason R, Waetzig Shelli R, Woerpel K A
Department of Chemistry, University of California, Irvine, California 92697-2025, USA.
Org Lett. 2009 Aug 6;11(15):3290-3. doi: 10.1021/ol901046z.
The cyclization of gamma,delta-unsaturated tertiary hydroperoxides in the presence of a palladium(II) catalyst afforded 1,2-dioxanes resembling biologically active natural products. A variety of substrates were screened, and synthetic manipulations were accomplished to construct compounds with structural similarity to antimalarial targets.
在钯(II)催化剂存在下,γ,δ-不饱和叔氢过氧化物的环化反应生成了类似于具有生物活性的天然产物的1,2-二氧六环。筛选了多种底物,并完成了合成操作以构建与抗疟靶点结构相似的化合物。