Hay Michael B, Wolfe John P
University of Michigan, Department of Chemistry, 930 N. University Ave, Ann Arbor, Michigan, 48109-1055.
Tetrahedron Lett. 2006 Apr 17;47(16):2793-2796. doi: 10.1016/j.tetlet.2006.02.066.
Pd-catalyzed carboetherifications of 1-, 2-, or 3-substituted γ-hydroxy internal alkenes afford tetrahydrofuran products bearing three stereocenters in good yield with moderate to good stereoselectivity.
钯催化的1-、2-或3-取代的γ-羟基内烯烃的碳醚化反应能够以良好的产率和中等至良好的立体选择性得到带有三个立体中心的四氢呋喃产物。