Li Junjun, Liu Yuxuan, Tang Weijun, Xue Dong, Li Chaoqun, Xiao Jianliang, Wang Chao
Key Laboratory of Applied Surface and Colloid Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, Shaanxi Normal University, Xi'an, 710119, P. R. China.
Department of Chemistry, University of Liverpool, Liverpool, L69 7ZD, UK.
Chemistry. 2017 Oct 17;23(58):14445-14449. doi: 10.1002/chem.201704037. Epub 2017 Sep 25.
The chemoselective alkylation and olefination of alkylnitriles with alcohols have been developed by simply controlling the reaction atmosphere. A binuclear rhodium complex catalyzes the alkylation reaction under argon through a hydrogen-borrowing pathway and the olefination reaction under oxygen through aerobic dehydrogenation. Broad substrate scope is demonstrated, permitting the synthesis of some important organic building blocks. Mechanistic studies suggest that the alkylation product may be formed through conjugate reduction of an alkene intermediate by a rhodium hydride, whereas the formation of olefin product may be due to the oxidation of the rhodium hydride complex with molecular oxygen.
通过简单地控制反应气氛,已开发出腈与醇的化学选择性烷基化和烯基化反应。一种双核铑配合物在氩气气氛下通过氢转移途径催化烷基化反应,在氧气气氛下通过需氧脱氢催化烯基化反应。该反应展示了广泛的底物范围,可用于合成一些重要的有机结构单元。机理研究表明,烷基化产物可能是通过氢化铑对烯烃中间体的共轭还原形成的,而烯烃产物的形成可能是由于氢化铑配合物与分子氧的氧化作用。