We have developed an asymmetric ring opening reaction of oxabenzonorbornadienes with substituted phenolic nucleophiles. Under the reaction conditions （ [Rh（COD）C1]2 （1 mol%）, （S）-（R）-PPF-P^Bu2 （2 mol%）, THF...We have developed an asymmetric ring opening reaction of oxabenzonorbornadienes with substituted phenolic nucleophiles. Under the reaction conditions （ [Rh（COD）C1]2 （1 mol%）, （S）-（R）-PPF-P^Bu2 （2 mol%）, THF, reflux）, the reaction products were obtained with high yield and enantiomeric excesses （ up to 99% ee）.展开更多
We have developed an asymmetric ring opening reaction of azabenzonorbornadiene with substituted piperazine. By increasing the amount of catalyst (from 2.5 to 5%) and ligands (5 to 10%) as well as addition of ammonium ...We have developed an asymmetric ring opening reaction of azabenzonorbornadiene with substituted piperazine. By increasing the amount of catalyst (from 2.5 to 5%) and ligands (5 to 10%) as well as addition of ammonium iodide, the products can be obtained in high yield and the reaction time shortened dramatically, but the ee values were rather low.展开更多
基金the Natural Science Foundation of Guangdong Province for financial support （No.04010404）.
文摘We have developed an asymmetric ring opening reaction of oxabenzonorbornadienes with substituted phenolic nucleophiles. Under the reaction conditions （ [Rh（COD）C1]2 （1 mol%）, （S）-（R）-PPF-P^Bu2 （2 mol%）, THF, reflux）, the reaction products were obtained with high yield and enantiomeric excesses （ up to 99% ee）.
文摘We have developed an asymmetric ring opening reaction of azabenzonorbornadiene with substituted piperazine. By increasing the amount of catalyst (from 2.5 to 5%) and ligands (5 to 10%) as well as addition of ammonium iodide, the products can be obtained in high yield and the reaction time shortened dramatically, but the ee values were rather low.
