448247-56-1Relevant academic research and scientific papers
Magnetically recyclable sepiolite/iron oxide/cupric oxide nanocomposite as a novel catalyst for the synthesis of S-aryl dithiocarbamates by C-S bond formation
Bagheri, Fatemeh Hassani,Khabazzadeh, Hojatollah,Fayazi, Maryam
, p. 1942 - 1953 (2021/07/10)
A convenient and efficient procedure is described for the synthesis of S-aryl dithiocarbamates by C-S bond formation through the coupling reaction of three components between secondary amines, carbon disulfide, and aryl iodides using magnetically separabl
A magnetically recyclable iron oxide-supported copper oxide nanocatalyst (Fe3O4-CuO) for one-pot synthesis of: S -aryl dithiocarbamates under solvent-free conditions
Aryanasab
, p. 32018 - 32024 (2016/04/26)
A green, convenient and efficient procedure is reported for the synthesis of S-aryl dithiocarbamates by a simple one-pot three component Ullmann-type condensation of an amine, carbon disulfide and an aryl iodide. Magnetically separable and reusable copper
Transition-Metal-Free C-S Bond Formation: Aqueous Synthesis of S-Aryl Dithiocarbamates by the use of Stable Arenediazonium Salts Mediated by Nano-Magnetic Supported Silica Sulfonic Acid
Nemati, Firouzeh,Elhampour, Ali,Zulfaghari, Soghra
, p. 1692 - 1702 (2015/09/15)
A convenient and transition-metal-free method for the synthesis of S-aryl dithiocarbamates based on the reaction of stable arenediazonium nano-magneto silica sulfates (ArN2+-OSO3-SiO2@Fe3O4) with dithiocarbamic acid at room temperature was studied. Avoiding the use of any hazardous transition metal, simple procedure, low cast, and short reaction time are noteworthy advantages of this methodology.
Reaction under ball-milling: Solvent-, ligand-, and metal-free synthesis of unsymmetrical diaryl chalcogenides
Mukherjee, Nirmalya,Chatterjee, Tanmay,Ranu, Brindaban C.
, p. 11110 - 11114 (2013/11/19)
A convenient, efficient, and general procedure for the synthesis of diaryl chalcogenides including sulfides, selenides and tellurides has been developed by the reaction of diazonium tetrafluoroborates and diaryl dichalcogenides on the surface of alumina u
Transition metal-free procedure for the synthesis of S-aryl dithiocarbamates using aryl diazonium fluoroborate in water at room temperature
Chatterjee, Tanmay,Bhadra, Sukalyan,Ranu, Brindaban C.
experimental part, p. 1837 - 1842 (2011/10/01)
A convenient, efficient and green procedure for the synthesis of S-aryl dithiocarbamates has been developed by a simple one-pot condensation of aryl diazonium fluoroborate, carbon disulfide and amine in the absence of any transition metal catalyst in water at room temperature. The reactions of a variety of substituted aryl diazonium fluoroborates, and cyclic and open chain amines, have been addressed. The products are purified by crystallization from ethanol and the process does not involve any hazardous solvent.
