Huang Shuai, Zhou Jianrong Steve
State Key Laboratory of Chemical Oncogenomics, School of Chemical Biology and Biotechnology, Peking University Shenzhen Graduate School, 2199 Lishui Road, Nanshan District, Shenzhen 518055, China.
J Am Chem Soc. 2024 May 15;146(19):12895-12900. doi: 10.1021/jacs.4c02818. Epub 2024 May 2.
A nickel complex of chiral bisoxazolines catalyzed the stereoselective reductive arylation of ketones in high enantioselectivity. A range of common acyclic and cyclic ketones reacted without the aid of directing groups. Mechanistic studies using isolated complex of a chiral bis(oxazoline) (L)Ni(Ar)Br revealed that Mn reduction was not needed, while Lewis acidic titanium alkoxides were critical to ketone insertion.
手性双恶唑啉镍配合物能够高效催化酮的立体选择性还原芳基化反应。一系列常见的开链和环状酮无需导向基团的辅助即可发生反应。对手性双(恶唑啉)(L)Ni(Ar)Br分离配合物进行的机理研究表明,无需锰还原,而路易斯酸性钛醇盐对酮的插入反应至关重要。