1093404-97-7Relevant academic research and scientific papers
Catalyst-free aqueous-mediated conjugative addition of indoles to β-nitrostyrenes
Habib, Pateliya Mujjamil,Kavala, Veerababurao,Kuo, Chun-Wei,Yao, Ching-Fa
, p. 7005 - 7007 (2008)
A catalyst free aqueous-mediated alkylation of indoles with various β-nitrostyrenes was performed at elevated temperature. No catalyst, clean reaction conditions, simple workup procedure, easy isolation, viability for large scale preparation, and environm
Iodine(III)-mediated tandem oxidative cyclization for construction of 2-nitrobenzo[ b ]furans
Lu, Shi-Chao,Zheng, Pu-Rong,Liu, Gang
supporting information, p. 7711 - 7717 (2012/10/29)
Various 3-alkyl-2-nitrobenzo[b]furans were synthesized from common intermediate 2-(2-nitroethyl)phenols via a hypervalent iodine-induced oxidative cyclization, with good to excellent yields. This facile route is able to efficiently functionalize 2-nitrobenzo[b]furans, which are difficult to obtain by classical methods.
Catalyst free conjugate addition of indoles and pyrroles to nitro alkenes under solvent free condition (SFC): An effective greener route to access 3-(2-nitro-1-phenylethyl)-1H-indole and 2-(2-nitro-1-phenylethyl)-1H-pyrrole derivatives
Habib, Pateliya Mujjamil,Kavala, Veerababurao,Kuo, Chun-Wei,Raihan, Mustafa J.,Yao, Ching-Fa
experimental part, p. 7050 - 7056 (2010/09/15)
Catalyst free conjugate addition of reactive hetero aromatics (pyrrole and indoles) to nitro alkenes under solvent free condition is described. This method provides several advantages, such as operational simplicity, solvent-free conditions and good yield
