| Literature DB >> 30624843 |
Guogang Deng1, Minyan Li2, Kaili Yu1, Chunxiang Liu1, Zhengfen Liu1, Shengzu Duan1, Wen Chen1, Xiaodong Yang1, Hongbin Zhang1, Patrick J Walsh2.
Abstract
Benzofurans are among the most popular structural units in bioactive natural products, however, the synthesis of such structures by radical cyclization cascade reactions is rare. Herein, we report a mild and broadly applicable method for the construction of complex benzofurylethylamine derivatives through a unique radical cyclization cascade mechanism. Single-electron transfer (SET) from 2-azaallyl anions to 2-iodo aryl allenyl ethers initiates a radical cyclization that is followed by intermolecular radical-radical coupling. This expedient approach enables the synthesis of a range of polycyclic benzofurans that would otherwise be difficult to prepare.Entities:
Keywords: azaallyl anions; benzofurylethylamine; cascade reactions; radical coupling; radical cyclization
Year: 2019 PMID: 30624843 DOI: 10.1002/anie.201812369
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336