1201683-18-2Relevant academic research and scientific papers
Copper(I)-catalyzed cascade synthesis of 2-arylsulfanyl-arylcyanamides
Sahoo, Santosh K.,Jamir, Latonglila,Guin, Srimanta,Patel, Bhisma K.
experimental part, p. 2538 - 2548 (2010/12/29)
We have developed a ligand-assisted copper(I)-catalyzed two sequential heteroarylation sequence. An intramolecular S-arylation is followed by an intermolecular N-arylation leading to the direct synthesis of N-aryl-2-aminobenzothiazoles. In most cases however, the 2-arylsulfanyl- arylcyanamide was the major product obtained via an intramolecular C-S bond formation, associated with C-S bond breakage, followed by an intermolecular S-arylation. The selectivity of this ligand-assisted reaction is quite different as compared to that of ligand-free reactions and the rates are much faster giving good yields of products. Various cyanamides can be prepared in excellent yields from their corresponding 1-substituted thioureas with or without the assistance of a ligand with a catalytic quantity of copper(I).
Copper-catalyzed domino intra- And intermodular C-S cross-coupling reactions: Synthesis of 2-(Arylthio)arylcyanamides
Ramana, Tamminana,Saha, Prasenjit,Das, Manas,Punniyamurthy, Tharmalingam
supporting information; experimental part, p. 84 - 87 (2010/03/03)
Chemical Equation Presented One-pot synthesis of 2-(arylthio)arylcyanamides is accomplished using cheap and air-stable CuSO 4·5H2O as a catalyst by domino intra- and intermolecular C-S cross-coupling reactions of 2-(iodoaryl)thioureas with aryl iodides under ligand-free conditions
