Saito Kodai, Horiguchi Kosaku, Shibata Yukihiro, Yamanaka Masahiro, Akiyama Takahiko
Department of Chemistry, Faculty of Science, Gakushuin University, 1-5-1 Mejiro, Toshima-ku, Tokyo 171-8588 (Japan).
Chemistry. 2014 Jun 16;20(25):7616-20. doi: 10.1002/chem.201402763. Epub 2014 May 6.
Chiral phosphoric acid catalyzed transfer hydrogenation of ketimines derived from propiophenone derivatives and reductive amination of alkyl ethyl ketone derivatives were extensively examined in the presence of two representative hydrogen donors. The excellent enantioselective transfer hydrogenation was achieved by use of benzothiazoline as a hydrogen donor. The theoretical studies elucidated that the unsymmetrical structure of benzothiazoline plays an important role in high enantioselective hydrogenation.
在手性磷酸催化下,以两种具有代表性的氢供体为介质,对源自苯丙酮衍生物的酮亚胺的转移氢化反应以及烷基乙基酮衍生物的还原胺化反应进行了广泛研究。以苯并噻唑啉作为氢供体,实现了优异的对映选择性转移氢化反应。理论研究表明,苯并噻唑啉的不对称结构在高对映选择性氢化反应中起着重要作用。