@article{d070f7b434114f1ab8cc51078cd2ed10,
title = "AgNTf2-mediated arylation of bromopyrroloindolines",
abstract = "The silver(I)-mediated arylation of bromopyrroloindolines was developed. The selection of silver salts was crucial to obtain arylated compounds in high yields. Among the various tested silver(I) salts, AgNTf2 was the most effective agent for arylation. Reactions using various electron-rich aromatic compounds revealed that the developed conditions are suitable for the arylation of a broad range of aromatic compounds, including benzene derivatives, furan, thiophene, and pyrrole.",
author = "Soichiro Sato and Azusa Hirayama and Tohma Adachi and Daichi Kawauchi and Hirofumi Ueda and Hidetoshi Tokuyama",
note = "Funding Information: This work was supported by JSPS KAKENHI Grant Numbers JP16H01127 in Middle Molecular Strategy and JP16H00999 in Precisely Designed Catalysts with Customized Scaffolding a Grant-in aid for Scientific Research (A) (26253001), the Platform Project for Supporting Drug Discovery and Life Science Research funded by Japan Agency for Medical Research and Development (AMED), and Astelals Foundation for Research on Metabolic Disorders. Publisher Copyright: {\textcopyright} 2017 The Japan Institute of Heterocyclic Chemistry.",
year = "2017",
doi = "10.3987/COM-17-13777",
language = "English",
volume = "94",
pages = "1940--1957",
journal = "Heterocycles",
issn = "0385-5414",
publisher = "Japan Institute of Heterocyclic Chemistry",
number = "10",
}