| Literature DB >> 27508407 |
Si Chen1, Xin-Xing Wu1, Jia Wang1, Xin-Hua Hao1, Yu Xia1, Yi Shen1, Huanwang Jing1, Yong-Min Liang1.
Abstract
A highly diastereoselective dearomatization of indoles via palladium-catalyzed decarboxylative alkynyl termination was developed. This protocol provides dissimilar tetracyclic and tetrasubstituted indoline scaffolds bearing congested stereocenters, which led to operationally simple conditions, short time, and broad substrate scope. Additionally, this reaction system could be scaled to gram quantities in a satisfactory yield and diastereoselectivity.Entities:
Year: 2016 PMID: 27508407 DOI: 10.1021/acs.orglett.6b01711
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005