Photochemical Preparation of 1,3,5,7-Tetracyanoadamantane and Its Conversion to 1,3,5,7-Tetrakis(aminomethyl)adamantane
作者:Ging S. Lee、Jude N. Bashara、Ghiwa Sabih、Asmik Oganesyan、Gayane Godjoian、Hieu M. Duong、Eric R. Marinez、Carlos G. Gutiérrez
DOI:10.1021/ol036526g
日期:2004.5.1
of 1,3,5,7-tetrabromoadamantane with cyanide produces 1,3,5,7-tetracyanoadamantane (1), which was reduced with borane reagents to 1,3,5,7-tetrakis(aminomethyl)adamantane (2). Improvements in the preparation of 1,3,5,7-tetrahaloadamantanes (halogen = Br, Cl, I) are also reported. [structure--see text]
已经制备了在所有四个桥头位置均具有官能化的一碳延伸的新的金刚烷衍生物1和2。1,3,5,7-四溴金刚烷与氰化物的自由基亲核取代(S(RN)1)反应产生1,3,5,7-四氰基金刚烷(1),该硼烷试剂将其还原为1,3,5, 7-四(氨基甲基)金刚烷(2)。还报道了在制备1,3,5,7-四氢金刚烷烷(卤素= Br,Cl,I)方面的改进。[结构-见文字]