摘要
由新?基环戊二烯和三甲基硅基环戊二烯制备了两个前手性的二茂锆配合物。由它们与亲核试剂的反应,合成了一些新的,手性在锆原子上的锆配合物。~1H NMR和^(13)C NMR谱图表明,配体上的手性基团对锆原子上的取代反应有明显的手性诱导效果。
From (+)-neomenthylcyclopentadiene and trimethylsilyl cyclopentadiene, a couple ofprochiral zirconocenes have been prepared. Upon further reactions with nucleophiles thesezirconocenes were transformed to chiral ones with chirality on the zirconium atom. TheNMR spectra of these complexes manifested that the chiral ligand had exerted a considerable chirally inductive effect during the course of the nucleophilic substitution.
出处
《有机化学》
SCIE
CAS
CSCD
北大核心
1993年第5期476-481,共6页
Chinese Journal of Organic Chemistry
基金
国家自然科学基金
关键词
手性二茂锆
手性诱导
制备
Chiral zirconocene
chiral induction
chirality on metal
peparation