State Key laboratory Base of Eco-chemical Engineering, College of Chemical Engineering, Qingdao University of Science and Technology, Qingdao 266042, China.
Molecules. 2019 Apr 21;24(8):1575. doi: 10.3390/molecules24081575.
A series of indane-based phosphine-oxazoline ligands with a spirocarbon stereogenic center were examined for palladium-catalyzed asymmetric allylic alkylation of indoles. Under optimized conditions, high yields (up to 98%) and enantioselectivities (up to 98% ee) were obtained with a broad scope of indole derivatives. The ligand was determined to be the most efficient P,N-ligand for this reaction. Moreover, the ligand was also efficient for Pd-catalyzed asymmetric allylic etherification with hard aliphatic alcohols as nucleophiles.
一系列基于茚满的磷-恶唑啉配体具有手性 spiro 碳中心,被用于钯催化吲哚的不对称烯丙基烷基化反应。在优化条件下,具有广泛取代吲哚衍生物的高收率(高达 98%)和对映选择性(高达 98%ee)被获得。该配体被确定为该反应最有效的 P,N-配体。此外,该配体对于 Pd 催化的不对称烯丙基醚化反应也具有较高的效率,硬脂族醇作为亲核试剂。