| Literature DB >> 29901864 |
Liwei Bu1, Jiangtao Li1, Yanli Yin1,2, Baokun Qiao1, Guobi Chai3, Xiaowei Zhao1, Zhiyong Jiang1.
Abstract
An enantioselective cascade aerobic oxidation and semipinacol rearrangement reaction of 2-aryl-3-alkyl-substituted indoles via visible-light-driven cooperative organophotoredox and H-bonding catalysis is reported. The current method provides an expedient and sustainable approach to furnish a variety of valuable chiral 2-aryl-2-alkyl-substituted indolin-3-ones in 64-90 % yield with 58-94 % ee. Preliminary control experiments present important insights into the stereochemistry.Entities:
Keywords: cooperative photoredox and asymmetric catalysis; indolin-3-ones; organocatalysis; oxidation; semipinacol rearrangement
Year: 2018 PMID: 29901864 DOI: 10.1002/asia.201800446
Source DB: PubMed Journal: Chem Asian J ISSN: 1861-471X