62497-30-7Relevant articles and documents
Sulfurative self-condensation of ketones and elemental sulfur: A three-component access to thiophenes catalyzed by aniline acid-base conjugate pairs
Nguyen, Thanh Binh,Retailleau, Pascal
supporting information, p. 387 - 390 (2018/02/07)
A sulfurative self-condensation method for constructing thiophenes 2 by a reaction between ketones 1 and elemental sulfur is reported. This reaction, which is catalyzed by anilines and their salts with strong acids, starts from readily available and inexp
Synthesis and properties of Z-1, 3-bis- (aryl)-4-bromo-2-buten-1-ones
Potikha,Turelik,Kovtunenko
experimental part, p. 1184 - 1189 (2010/05/18)
Bromination of 1, 3-bis(aryl)-2-buten-1-ones by N-bromosuccinimide in anhydrous carbon tetrachloride gives Z-1, 3-bis(aryl)-4-bromo-2-buten-1-ones. The effect of the nature of substituent in the benzene ring on the course of a reaction with nucleophiles h
The dimerization of 2,5-diaryl-1,4-dithiin radical cations
Andersen, Mogens Larsen,Nielsen, Merete Folmer,Hammerich, Ole
, p. 94 - 107 (2007/10/03)
The electrochemical oxidation of five 2,5-diaryl-1,4-dithiins with aryl = p-anisyl (BAD), p-tolyl (BTD), phenyl (DPD), p-chlorophenyl (BCD) and p-nitrophenyl (BND) has been studied in MeCN-CH2Cl2 (1:1) by cyclic voltammetry (CV), der