3β-Hydroxy-5α-androstan-17-one, (+)-camphor, and (–)-menthone have been converted into the corresponding spiro-hydantoins by the Bucherer synthesis. The reaction failed with cholestan-7-one, cholest-4-en-3-one, and 17α,21-dihydroxy-5α-pregnane-3,11,20-tri-one 3,20-disemicarbazone. Efforts to obtain steroid dihydantoins were unsuccessful. Deamination of camphane and menthane amino-acids provides evidence
通过Bucherer合成,将3β-Hydroxy-5α-androstan-17-one,(+)-
樟脑和(-)-
薄荷酮转化为相应的螺乙内酰
脲。反应失败的是胆甾烷7-1,胆甾烯4-en-3-one和17α,21-二羟基-5α-孕烯-3,11,20-三酮3,20-双半碳zone。获得类
固醇二乙内酰
脲的努力未成功。
樟脑和薄荷烷
氨基酸的脱
氨基提供了其构型的证据。