立体中心
催化作用
化学
对称化
产量(工程)
配体(生物化学)
炔烃
芳基
金属
铥
药物化学
晶体结构
磷化氢
烷基
立体化学
对映选择合成
有机化学
材料科学
受体
冶金
光电子学
兴奋剂
生物化学
作者
Yu Zhang,Fengcai Zhang,Long Chen,Jian Xu,Xiaohua Liu,Xiaoming Feng
标识
DOI:10.1021/acscatal.9b00860
摘要
A chiral thulium(III)-catalyzed sulfur-conjugation addition reaction of dialkynylphosphine oxides to construct P-stereogenic centers has been developed. Dialkynylphosphine oxides bearing aryl, alkyl, alkenyl substitution at the alkyne terminus position were tolerated under the reaction conditions. The corresponding P,S-containing compounds were obtained in moderate to good yields (up to 92% yield) with high Z/E ratios and enantioselectivities (up to >95/5 Z/E and 97% ee), which could be transformed into versatile optically active phosphine oxide derivatives. X-ray single crystal structures of chiral N,N′-dioxides with rare-earth metal triflates revealed how the metal center and ligand structure affect the enantioselectivity.
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