Tricyclic oxonium-directed addition : regiochemistry and stereochemistry of the iodination reactions in 2,3-epoxy cyclooct-5-en-1-ols and 2,3-epoxy-5-en-1-one
暂无分享,去创建一个
[1] C. Ruiz-Pérez,et al. Tricyclic oxonium-directed addition: Regiochemistry and stereochemistry of the electrophilic additions to epoxy cycloalkenols. , 1988 .
[2] C. Ruiz-Pérez,et al. Synthesis of cyclic ethers via 5-exo iodonium assisted epoxide ring expansion. , 1988 .
[3] K. Sharpless,et al. Catalytic asymmetric epoxidation and kinetic resolution: modified procedures including in situ derivatization , 1987 .
[4] V. Martín,et al. Stereo and regioselective openings of chiral 2,3-epoxy alcohols. Versatile routes to optically pure natural products and drugs. Unusual kinetic resolutions , 1983 .
[5] K. Jitsukawa,et al. Vanadium-catalyzed epoxidation of cyclic allylic alcohols. Stereoselectivity and stereocontrol mechanism , 1979 .
[6] T. S. Cantrell,et al. Photochemistry of 2,6-cyclooctadienone and 2,4-cyclooctadienone , 1970 .
[7] C. Walling,et al. The Copper-Catalyzed Reaction of Peresters with Hydrocarbons , 1963 .