Iijima I, Minamikawa J, Jacobson A E, Brossi A, Rice K C
J Med Chem. 1978 Apr;21(4):398-400. doi: 10.1021/jm00202a018.
(+)-Naloxone was prepared in 26% overall yield in eight steps from (+)-7-bromodihydrocodeinone dimethyl ketal by a synthesis which excluded enantiomeric contamination. (+)-Naloxone was examined in three assay systems and found to have no more than 1/1000(-1)/10 000th the activity of (-)-naloxone; it can, thus, serve to test the stereospecificity of the biochemical and pharmacological actions of (-)-naloxone.
(+)-纳洛酮以(+)-7-溴二氢可待因酮二甲基缩酮为原料,经八步反应合成,总收率为26%,该合成方法避免了对映体污染。在三种分析系统中对(+)-纳洛酮进行了检测,发现其活性不超过(-)-纳洛酮的1/1000至1/10000;因此,它可用于测试(-)-纳洛酮生化和药理作用的立体特异性。