Catalytic asymmetric bromochlorination of aromatic allylic alcohols promoted by multifunctional Schiff base ligands†
Wei-Sheng Huang,Li Chen,Zhan-Jiang Zheng,Ke-Fang Yang,Zheng Xu,Yu-Ming Cui
Organic & Biomolecular Chemistry Pub Date : 07/28/2016 00:00:00 , DOI:10.1039/C6OB01306F
Abstract

It was found that the tridentate O,N,O-type Schiff base ligand bearing suitable substituents was a highly effective promoter in the catalytic asymmetric bromochlorination reaction, in which the corresponding aromatic bromochloroalcohols with vicinal halogen-bearing stereocenters were formed with perfect regioselectivity, with moderate to excellent enantioselectivities (up to 93% ee), and with good yields and chemoselectivities.

Graphical abstract: Catalytic asymmetric bromochlorination of aromatic allylic alcohols promoted by multifunctional Schiff base ligands