70838-54-9Relevant academic research and scientific papers
A convenient and efficient copper-catalyzed synthesis of unsymmetrical and symmetrical diaryl chalcogenides from arylboronic acids in ethanol at room temperature
Kumar, Amit,Kumar, Sangit
, p. 1763 - 1772 (2014/03/21)
A simple and convenient approach for the synthesis of unsymmetrical diaryl chalcogenides (Te, Se, and S) has been developed by copper-catalyzed cross-coupling reaction of organoboronic acid with diaryl dichalcogenide in ethanol using NaBH4 in air or oxygen. The present methodology is highly practical for the synthesis of unsymmetrical diaryl tellurides with various functionalities such as -NO2, -F, -Br, and -COOH that have been obtained in good to excellent yields. Methodology is also effective for the synthesis of unsymmetrical diaryl selenides and sulfides. Moreover, symmetrical diaryl selenides have also been obtained from arylboronic acids using elemental selenium powder under optimized reaction conditions. The use of NaBH 4 is the key for the development of milder reaction conditions, which enable the construction of unsymmetrical diaryl chalcogenides from boronic acid substrates in ethanol at room temperature.
Microwave-assisted reaction of aryl diazonium fluoroborate and diaryl dichalcogenides in dimethyl carbonate: A general procedure for the synthesis of unsymmetrical diaryl chalcogenides
Kundu, Debasish,Ahammed, Sabir,Ranu, Brindaban C.
experimental part, p. 2024 - 2030 (2012/07/17)
A convenient, general and efficient procedure for the synthesis of unsymmetrical diaryl chalcogenides has been developed by the reaction of aryl diazonium fluoroborates and diaryl dichalcogenides in the presence of zinc dust in dimethyl carbonate under microwave irradiation. The reactions of a wide range of substituted aryl diazonium fluoroborates and diaryl dichalcogenides have been addressed. The zinc dust is required for the cleavage of diaryl dichalcogenides. The products are obtained in high purity after fast column chromatography of the crude residue after evaporation of dimethyl carbonate. The Royal Society of Chemistry 2012.
Microwave-assisted copper-catalyzed preparation of diaryl chalcogenides
Kumar, Sangit,Engman, Lars
, p. 5400 - 5403 (2007/10/03)
Diaryl chalcogenide synthesis employing diaryl dichalcogenides and aryl halides as starting materials in the presence of excess magnesium and a catalytic amount of CuI/bipyridyl is significantly improved by microwave heating. Reaction times can be reduced from 2 to 3 days to 6-8 h. Both aryl bromides and aryl chlorides can be used as substrates in the substitution reaction. The procedure is useful not only for diaryl sulfide and diaryl selenide synthesis but also for the preparation of unsymmetrical diaryl tellurides. Starting from suitable aryl halides, the novel microwave-assisted procedure was used for the facile preparation of novel chalcogen analogues (PhS-, PhSe-, and PhTe-) of various antioxidants (ethoxyquin and 3-pyridinol). Attempts to use dialkyl dichalcogenides for the coupling of alkylchalcogeno moieties to aryl halides were only successful in the case of long-chain (such as n-octyl) disulfides and diselenides.
SRN1 reaction of haloarenes with benzenethiolate, benzeneselenolate, and benzenetellurolate ions promoted by Sml2
Zhang, Yongmin
, p. 539 - 541 (2007/10/03)
SRN1 reaction is of haloarenes with benzenethiolate, benzeneselenate, and benzenetellurolate ions can be carried out by use of samarium diiodide (SmI2) as a promoter in DMF-THF to afford the corresponding ArZPh compounds in moderate to good yields.
Synthesis and X-Ray Structure of 1,8-Bis(phenyltelluro)naphthalene and Its Peri Tellurium-Tellurium Interaction
Fujihara, Hisashi,Ishitani, Hideya,Takaguchi, Yutaka,Furukawa, Naomichi
, p. 571 - 572 (2007/10/03)
New 1,8-diaryl and dialkyl substituted ditelluronaphthalenes, 1,8-bis(phenyltelluro)naphthalene (1) and 1,8-bis(butyltelluro)naphthalene, have been synthesized.The cyclic voltammogram of 1 showed the reversible electrochemical oxidation with remarkably lo
