119345-53-8Relevant academic research and scientific papers
Efficient synthesis of unsymmetrical heteroaryl thioethers and chalcogenides by alkali hydroxide-mediated SNAr reactions of heteroaryl halides and dichalcogenides
Ma, Xiantao,Liu, Quan,Jia, Xiaojuan,Su, Chenliang,Xu, Qing
, p. 56930 - 56935 (2016)
An efficient alkali hydroxide-mediated SNAr reaction of heteroaryl halides has been developed for the practical synthesis of the useful unsymmetrical heteroaryl thioethers and chalcogenides. The usually odorless, easily available, lowly toxic, and easily stored and handled diorganyl dichalcogenides can be used as safer and convenient chalcogen nucleophile precursors and diverse unsymmetrical heteroaryl chalcogenides can be obtained in good to high yields by the method.
Glycerol/hypophosphorous acid: An efficient system solvent-reducing agent for the synthesis of 2-organylselanyl pyridines
Thurow, Samuel,Webber, Rodrigo,Perin, Gelson,Lenard?o, Eder J.,Alves, Diego
supporting information, p. 3215 - 3218 (2013/06/27)
We describe herein an efficient and simple method to synthesize 2-organylselanyl pyridines by reactions of 2-chloropyridines with organylselenols, generated in situ by reaction of diorganyl diselenides, using glycerol as solvent and hypophosphorous acid (
THE SYNTHESIS OF BIS(PHENYLSELENENYL), BIS(ALKYELSELENENYL)PYRIDINES AND OF PYRIDYLSELENOLATE ANIONS
Tiecco, Marcello,Testaferri, Lorenzo,Tingoli, Marco,Chianelli, Donatella,Bartoli, Donatelle,Balducci, Roberta
, p. 4883 - 4894 (2007/10/02)
The reactions of several dihalogenopyridines with PhSeNa or MeSeLi in DMF afforded the monosubstitution products in good yields.With excess PhSeNa the bis(phenylselenenyl)pyridines were easily obtained, Whereas with excess MeSeLi the initially formed halo
