A highly efficient and selective[2+2+2]cyclization of diynes and monoalkynes was catalyzed by rhodium under room temperature in water/THF mixed solvent,affording isoindolines and isobenzofurans in good to excellent yi...A highly efficient and selective[2+2+2]cyclization of diynes and monoalkynes was catalyzed by rhodium under room temperature in water/THF mixed solvent,affording isoindolines and isobenzofurans in good to excellent yields.The center atoms (N,O) in the diynes showed a significant effect for the cyclization.展开更多
A new method for preparation of N-tosylimines by InCl_3-mediated condensation of aldehydes with p-toluenesulfonamide in refluxing benzene is reported.The procedure is lauded by its simplicity,mild reaction conditions,...A new method for preparation of N-tosylimines by InCl_3-mediated condensation of aldehydes with p-toluenesulfonamide in refluxing benzene is reported.The procedure is lauded by its simplicity,mild reaction conditions,excellent yields and adaptability to electron deficient and electron rich aromatic,andα,β-unsaturated aldehydes.展开更多
文摘A highly efficient and selective[2+2+2]cyclization of diynes and monoalkynes was catalyzed by rhodium under room temperature in water/THF mixed solvent,affording isoindolines and isobenzofurans in good to excellent yields.The center atoms (N,O) in the diynes showed a significant effect for the cyclization.
文摘A new method for preparation of N-tosylimines by InCl_3-mediated condensation of aldehydes with p-toluenesulfonamide in refluxing benzene is reported.The procedure is lauded by its simplicity,mild reaction conditions,excellent yields and adaptability to electron deficient and electron rich aromatic,andα,β-unsaturated aldehydes.
