Nucleophilic addition to vinylketene- and vinylketenimine (allenylideneamine)tricarbonyliron(0) complexes
作者:Lawrence Hill、Christopher J. Richards、Susan E. Thomas
DOI:10.1039/c39900001085
日期:——
Nucleophiles add to C-1 of (vinylketene)tricarbonyliron(0) complexes to give β,γ-unsaturated carbonyl derivatives, whereas nucleophilic attack on a (vinylketenimine)tricarbonyliron(0) analogue occurs at C-2 and leads, after an oxidative work-up, to β,γ-unsaturated amides containing an a quaternary centre.
亲核试剂添加到(乙烯基乙烯酮)三羰基铁(0)配合物的C-1中,生成β,γ-不饱和羰基衍生物,而对(乙烯基乙烯亚胺)三羰基铁(0)类似物的亲核攻击发生在C-2处,并在氧化作用后产生到含有一个季中心的β,γ-不饱和酰胺。