Nakamura Shuichi, Tokunaga Akari, Saito Hikari, Kondo Masaru
Department of Life Science and Applied Chemistry, Graduate School of Engineering, Nagoya Institute of Technology, Gokiso, Showa-ku, Nagoya 466-8555, Japan.
Chem Commun (Camb). 2019 May 10;55(37):5391-5394. doi: 10.1039/c9cc02443c. Epub 2019 Apr 18.
The enantioselective conjugate addition reaction of an α,α-dithioacetonitrile with nitroalkenes was catalysed by chiral bis(imidazoline)-palladium pincer-type complexes. The reaction was applicable to various nitroalkenes to afford products in good yield with high enantioselectivity. The obtained products can be converted to γ-lactam and biologically active rolipram.
手性双(咪唑啉)-钯钳型配合物催化α,α-二硫代乙腈与硝基烯烃的对映选择性共轭加成反应。该反应适用于各种硝基烯烃,能以高对映选择性得到高产率的产物。所得产物可转化为γ-内酰胺和具有生物活性的咯利普兰。