Palladium-Catalyzed Dearomatizing Difunctionalization of Indoles and Benzofurans was written by Ramella, Vincenzo;He, Zhiheng;Daniliuc, Constantin G.;Studer, Armido. And the article was included in European Journal of Organic Chemistry in 2016.Product Details of 62119-70-4 This article mentions the following:
A palladium-catalyzed dearomatizing difunctionalization of N-Boc-indoles and benzofurans to give tricyclic indolines and 2,3-dihydrobenzofurans with a fully substituted carbon center was described. Product formation occurred under mild conditions at room temperature with com. available aryl boronic acids and 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) as a mild oxidant in good yields. In the experiment, the researchers used many compounds, for example, 2-Benzofuranacetic acid (cas: 62119-70-4Product Details of 62119-70-4).
2-Benzofuranacetic acid (cas: 62119-70-4) belongs to benzofurans derivatives. Benzofurans are only weakly aromatic in nature and they are cleaved by many oxidative and reductive conditions. Substituted benzofurans find applications such as fluorescent sensors, oxidants, in drug discovery, and in another field of chemistry and agriculture.Product Details of 62119-70-4
Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem