首页> 外文期刊>Organic letters >Photochemical preparation of 1,3,5,7-Tetracyanodadamantane and Its Conversion to 1,3,5,7-Tetrkis(aminomethyl)damantane
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Photochemical preparation of 1,3,5,7-Tetracyanodadamantane and Its Conversion to 1,3,5,7-Tetrkis(aminomethyl)damantane

机译:1,3,5,7-四氰基金刚烷的光化学制备及其向1,3,5,7-四(氨基甲基)金刚烷的转化

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摘要

New adamantane derivatives1 and 2 that bear functionalized oen-carbon extensions at all four bridgehead positions have been prepared.Radical nucleophilic substitution(S_(RN1)reaction of 1,3,5,7-tetrabromoadamntane with cyanide produces 1,3,5,7-tetracyanoadamantane(1),which was reduced iwth borane reagents to 1,3,5,7-tetrakis(aminomethyl)adamantane(2).Improvements in the preparation of 1,3,5,7-tetrahaloadamantane(Halogen=Br,Cl,I)are also reported.
机译:制备了在所有四个桥头位置均具有官能化的碳-碳延伸的新的金刚烷衍生物1和2.自由基1,3,5,7-四溴金刚烷与氰化物的自由基亲核取代(S_(RN1)反应产生1,3,5,7 -四氰基金刚烷(1),经硼烷试剂还原为1,3,5,7-四(氨基甲基)金刚烷(2)。制备1,3,5,7-四ha金刚烷(卤素= Br,Cl ,我)也有报道。

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