852211-41-7Relevant academic research and scientific papers
A method for accessing sulfanylfurans from homopropargylic alcohols and sulfonyl hydrazides
Yan, Rulong,Yang, Xiaodong
supporting information, p. 3571 - 3574 (2019/06/13)
A sulfenylation/cyclization reaction has been developed for the synthesis of sulfanylfurans in the presence of iodine. These processes provide facile strategies to construct C-S/O bonds, and expand the methods of synthesizing sulfanylfurans. In this trans
Microwave-assisted zinc chloride-catalyzed synthesis of substituted pyrroles from homopropargyl azides
Wyrebek, Przemys?aw,Sniady, Adam,Bewick, Nicholas,Li, Yan,Mikus, Agnieszka,Wheeler, Kraig A.,Dembinski, Roman
experimental part, p. 1268 - 1275 (2009/04/10)
Ligand-free 5-endo-dig cyclization of 1,4- and 1,2,4-substituted but-3-yn-1-yl (homopropargyl) azides in the presence of zinc chloride (usually 20 mol %) in dichloroethane at elevated temperature provides 2,5-di- and 2,3,5-trisubstituted pyrroles in high
5-Endo-dig electrophilic cyclization of 1,4-disubstituted but-3-yn-1-ones: Regiocontrolled synthesis of 2,5-disubstituted 3-bromo- and 3-iodofurans
Sniady, Adam,Wheeler, Kraig A.,Dembinski, Roman
, p. 1769 - 1772 (2007/10/03)
(Chemical Equation Presented) 5-Endo-dig electrophilic cyclization of 1,4-diaryl but-3-yn-1-ones with N-bromosuccinimide or N-iodosuccinimide/acetone and iodine monochloride/ CH2Cl2, at room temperature, in the absence of base, provi
