| Literature DB >> 32786647 |
Lei Zhang1, Junyu Chen1, Tianshuo Zhong1, Xiangyun Zheng1, Jian Zhou1, Xinpeng Jiang1, Chuanming Yu1.
Abstract
A novel palladium-catalyzed [2 + 2 + 1] annulation of alkyne-tethered aryl iodides with diaziridinone was developed, leading to the formation of 3,4-fused tricyclic indoles. From a mechanistic standpoint, the formation of fused tricyclic indole scaffolds involved C,C-palladacycles, which were synthesized through the intramolecular reaction of aryl halides and alkynes. The cascade reaction described herein could be carried out with a broad range of substrates and provided various 3,4-fused tricyclic indoles with yields up to 98%.Entities:
Year: 2020 PMID: 32786647 DOI: 10.1021/acs.joc.0c01365
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354