Production of (-)dodecahydro-3a,6,6,9a-tetramethyl-naphtho[2,1-b] furan
    2.
    发明授权
    Production of (-)dodecahydro-3a,6,6,9a-tetramethyl-naphtho[2,1-b] furan 失效
    ( - )十二氢-3a,6,9,9-四甲基 - 萘并[2,1-b]呋喃的生产

    公开(公告)号:US5473085A

    公开(公告)日:1995-12-05

    申请号:US314507

    申请日:1994-09-28

    IPC分类号: C07D307/92

    CPC分类号: C07D307/92

    摘要: Preparation of a methyl ketone intermediate useful in the synthesis of (-)-dodecahydro-3a,6,6, 9a-tetramethyl-naphtho(2,1-b) furan by subjecting (-)-sclareol to ozonolysis in the presence of iodine or iodine-containing compound. The intermediate can be converted to (-)-dodecahydro-3a,6,6,9a-tetramethyl-naphtho(2,1-b) furan by Baeyer-Villiger oxidation followed by reduction of the resulting product in the presence of a Lewis acid.

    摘要翻译: ( - ) - 十二氢-3a,6,6,9a-四甲基萘并(2,1-b)呋喃的合成中使用( - ) - 香紫苏醇在碘存在下进行臭氧分解的甲基酮中间体的制备 或含碘化合物。 可以通过Baeyer-Villiger氧化将中间体转化为( - ) - 十二氢-3a,6,6,9a-四甲基萘并(2,1-b)呋喃,然后在路易斯酸存在下还原所得产物 。