A high yielding method was accomplished for the synthesis of polyfunctionally-substituted carboranes by the Michael addition reaction of various carbon- and boron carborane nucleophiles with α,β-unsaturated compounds containing an electron withdrawing group using Triton-B (benzyltrimethylammonium hydroxide) as a catalyst. This method of synthesizing carborane derivatives involves mild conditions, simple
以 Triton-B(
苄基三甲基氢氧化铵)为催化剂,通过各种碳和
硼碳
硼烷亲核试剂与含吸电子基团的 α,β-不饱和化合物的迈克尔加成反应,实现了一种高产率的多官能取代碳
硼烷的合成方法. 这种合成碳
硼烷衍
生物的方法条件温和,程序简单,产品收率高。结果,获得并充分表征了一系列官能化的碳
硼烷化合物。