75160-57-5Relevant academic research and scientific papers
N,N′-Mono substituted acyclic thioureas: Efficient ligands for the palladium catalyzed Heck reaction of deactivated aryl bromides
Keesara, Srinivas,Parvathaneni, Saiprathima,Mandapati, Mohan Rao
, p. 6769 - 6772 (2015/05/05)
A series of N,N′-mono substituted acyclic thiourea ligands are found to be highly active phosphine-free catalysts for palladium catalyzed Heck reaction of aryl iodides and bromides with olefins. We have achieved high turnover numbers for aryl iodides with olefins (TONs up to 970,000 for the reaction of iodobenzene with styrene).
Cytotoxicity and QSAR study of (thio)ureas derived from phenylalkylamines and pyridylalkylamines
Pingaew, Ratchanok,Tongraung, Pan,Worachartcheewan, Apilak,Nantasenamat, Chanin,Prachayasittikul, Supaluk,Ruchirawat, Somsak,Prachayasittikul, Virapong
, p. 4016 - 4029 (2013/07/26)
Simplified 1,3-disubstituted urea derivatives (11-24) of phenylethylamines, homoveratylamines, 2-pyridylethylamines, 2-picolylamines as well as xylylenediamines were synthesized and investigated for their cytotoxic activities. The results revealed that mo
Polycyclic Azines. III (1). Synthesis of 3-Aminoimidazopyridine Derivatives by Cyclodesulfurization of N'-Substituted-N-(2-pyridylmethyl)thioureas with Dicyclohexylcarbodiimide (2,3)
Bourdais, J.,Omar, A.-Mohsen M. E.
, p. 555 - 558 (2007/10/02)
A series of 3-substituted aminoimidazopyridine derivatives have been synthesized by cyclodesulfurization of a variety of N'-substituted-N-(2-pyridylmethyl)thioureas with dicyclohexylcarbodiimide (DCCD). 1H Nmr spectral analysis of all synthesized c
