重氮
烯醇
烷基化
化学
产量(工程)
催化作用
分子间力
药物化学
有机化学
分子
材料科学
冶金
作者
Brett D. McLarney,Marchello A. Cavitt,Theodore M. Donnell,Djamaladdin G. Musaev,Stefan France
标识
DOI:10.1002/chem.201604518
摘要
Abstract A Rh II ‐catalyzed method for intermolecular alkylation of the β‐C(sp 2 )−H bond of enol ethers, enamides, and enecarbamates with α‐diazo‐1,3‐dicarbonyl compounds is reported. The products are formed in up to 99 % yield and can be readily derivatized under a variety of conditions. By utilizing a combination of experimental and computational studies, the presumptive addition–elimination reaction mechanism was investigated and found to proceed under thermodynamic control at higher temperature. The acquired fundamental knowledge was translated into a strategic reaction design and yielded the first example of the β‐C−H functionalizations of acyclic enol ethers using α‐diazo‐1,3‐dicarbonyl compounds.
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