71972-86-6Relevant academic research and scientific papers
Furan ring opening-indole ring closure: SnCl2-induced reductive transformation of difuryl(2-nitroaryl)methanes into 2-(2-acylvinyl)indoles
Uchuskin, Maxim G.,Molodtsova, Natalia V.,Abaev, Vladimir T.,Trushkov, Igor V.,Butin, Alexander V.
experimental part, p. 4252 - 4258 (2012/07/14)
A simple and efficient method for the synthesis of 2-(2-acylvinyl)-3-(5- alkyl-2-furyl)indoles by reductive recyclization of bis(5-alkyl-2-furyl)(2- nitroaryl)methanes is reported. This transformation was carried out by heating the substrates with SnClsu
Intramolecular Nitrene Insertions into Aromatic and Heteroaromatic Systems. Part 6. Insertion with o-Nitrenophenyldithienyl methanes.
Hayes, Peter C.,Jones, Gurnos,Keates, Claire,Kladko, Irene,Radley, Peter
, p. 3523 - 3535 (2007/10/02)
The preparation of four o-nitrophenyldithienylmethanes (2a) - (2d), and of the amines (3a) and (3d), and azides (4a) and (4d) is described.Deoxygenation of the nitro compounds, or decomposition of the azides, gave 2-aminophenyldithienylmethanes (3a) - (3d
