Department of Process Research, Merck Frosst Centre for Therapeutic Research, 16711 Route Trans-Canadienne, Kirkland, Québec, Canada H9H 3L1.
J Am Chem Soc. 2011 Mar 9;133(9):2878-80. doi: 10.1021/ja111540g. Epub 2011 Feb 10.
The highly enantioselective catalytic asymmetric addition of aryl and alkenylboronic acids to N-benzylnicotinate salt 1 is described. The dihydropyridine 2 reaction products can be converted to synthetically useful piperidines. Application of the methodology to the preparation of enantioenriched quaternary chiral centers is also discussed.
描述了芳基和烯基硼酸对 N-苄基烟酸盐 1 的高对映选择性催化不对称加成。二氢吡啶 2 的反应产物可以转化为合成上有用的哌啶。该方法学在制备对映体富集的季碳手性中心中的应用也进行了讨论。