Faculty of Pharmacy, Meijo University, 150 Yagotoyama, Nagoya 468-8503, Japan.
Chem Commun (Camb). 2013 May 11;49(38):4030-2. doi: 10.1039/c3cc41789a. Epub 2013 Apr 5.
A bis(thiourea) organocatalyst with a planar chiral [2.2]paracyclophane backbone has been synthesized and applied to the Henry reaction. The obtained high reactivity and enantioselectivity from the reaction of aromatic aldehydes with nitroalkanes suggested the significant potential of [2.2]paracyclophane to serve as the backbone of the organocatalyst.
一种具有平面手性[2.2]对环芳烷骨架的双(硫脲)有机催化剂已被合成并应用于 Henry 反应。从芳香醛与硝基烷的反应中获得的高反应活性和对映选择性表明[2.2]对环芳烷作为有机催化剂骨架具有重要的潜力。