作者:Rohidas S. Sulake、Chinpiao Chen、Huei-Ru Lin、Ahai-Chang Lua
DOI:10.1016/j.bmcl.2011.08.021
日期:2011.10
A convenient synthesis of ketamine metabolite dehydronorketamine-d4, starting from commercially available deuterium labeled bromochlorobenzene, was achieved. Key steps include Grignard reaction, regioselective hydroxybromination, Staudinger reduction, and dehydrohalogenation.
从市售氘标记的溴氯苯开始,可以方便地合成氯胺酮代谢物脱氢去氧氯胺酮d 4。关键步骤包括格氏反应,区域选择性羟基溴化,施陶丁格还原和脱卤化氢。