Department of Frontier Materials, Graduate School of Engineering, Nagoya Institute of Technology, Gokiso, Showa-ku, Nagoya 466-8555, Japan.
Chemistry. 2013 Mar 25;19(13):4128-34. doi: 10.1002/chem.201203782. Epub 2013 Feb 27.
Manifold products: The enantioselective decarboxylative Mannich-type reaction of cyanoacetic acid with N-(2-pyridinesulfonyl)imines catalyzed by chiral 1,3-bis(imidazolin-2-yl)benzene (Phebim)-Pd(II) complexes afforded products with good enantioselectivity (see scheme). The reaction was applied to a wide range of imines with good yield and enantioselectivity. The obtained products can be converted into various compounds without the loss of enantiopurity.
手性 1,3-双(咪唑啉-2-基)苯(Phebim)-Pd(II) 配合物催化氰基乙酸与 N-(2-吡啶磺酰)亚胺的对映选择性脱羧 Mannich 型反应,得到具有良好对映选择性的产物(见方案)。该反应适用于具有良好产率和对映选择性的各种亚胺。得到的产物可以在不损失对映纯度的情况下转化为各种化合物。