Tomohara Keisuke, Kasamatsu Koji, Yoshimura Tomoyuki, Furuta Takumi, Kawabata Takeo
Institute for Chemical Research, Kyoto University.
Chem Pharm Bull (Tokyo). 2016 Jul 1;64(7):899-906. doi: 10.1248/cpb.c16-00272. Epub 2016 May 3.
Enantioselective intramolecular conjugate addition reactions of short-lived C-O axially chiral enolates have been developed. The reactions proceeded with inversion of the configuration and provided dihydrobenzofurans with contiguous tetra- and trisubstituted carbon centers in up to 96% enantiomeric excess (ee).
已开发出短寿命的C-O轴手性烯醇盐的对映选择性分子内共轭加成反应。反应以构型翻转的方式进行,并提供具有连续四取代和三取代碳中心的二氢苯并呋喃,对映体过量(ee)高达96%。