22454-49-5Relevant academic research and scientific papers
Copper catalyzed cyanomethylation reaction of 4-thiazolidinone
Chauhan, Prakashsingh M.,Morja, Mayur I.,Asamdi, Manjoorahmed,Chikhalia, Kishor H.
, (2020)
An effective copper catalyzed Cross Dehydrogenative Coupling (CDC) reaction of 4-thiazolidinones with acetonitrile has been developed. The described strategy undergoes radical pathway by employing copper, oxidant and easily available acetonitrile as a cya
Synthesis, spectral and structural study of sulfur-containing copper(II) complexes
Patel,Singh,Shukla,Patel,Sondhiya,Dwivedi
, p. 299 - 313 (2010)
A series of four new copper(II) complexes [Cu(H2L)(L1)] 1, [Cu(H2L)(PMDT)] 2, [Cu(H2L)(Dien)] 3 and [Cu(H 2L)(L2)] 4 have been synthesized by template condensation (H2L=thiodiglycolic acid,
Palladium-Catalyzed Carbonylative Synthesis of 3-Methyleneisoindolin-1-ones from Ketimines with Hexacarbonylmolybdenum(0) as the Carbon Monoxide Source
Wang, Zechao,Zhu, Fengxiang,Li, Yahui,Wu, Xiao-Feng
, p. 94 - 98 (2017/01/17)
An interesting procedure for the palladium-catalyzed carbonylative synthesis of 3-methyleneisoindolin-1-ones from ketimines was established. By using Mo(CO)6 (0.3 equiv.) as the solid CO source and through C(sp2)?H bond activation, t
Antihyperglycemic, α-glucosidase inhibitory and DPPH free radical scavenging activity of 5-bromosalicylaldehyde and schiff bases
Misra, Sristicheta,Pandeya, Krishna Bihari,Tiwari, Ashok Kumar,Ali, Amtul Zehra,Saradamani, Thimmapatruni,Agawane, Sachin Bharat,Madhusudana, Kuncha
experimental part, p. 1431 - 1437 (2012/05/20)
α-Glucosidase inhibition and DPPH free radical scavenging by 5-bromosalicylaldehyde and some Schiff bases have been measured. 5-Bromosalicylaldehyde shows lowest IC50 value (8.80 μM) for α-glucosidase inhibition and also shows good results in in vivo experiments for antihyperglycemic potential. Springer Science+Business Media, LLC 2010.
Structural modifications of the primary amino group of anticonvulsant aryl semicarbazones
Dimmock,Puthucode,Lo,Quail,Yang,Stables
, p. 83 - 88 (2007/10/02)
A number of aryl semicarbazones had been shown previously to possess significant anticonvulsant properties. The principal objective of the present investigation was to determine the importance of the primary amino group in this series of compounds by replacing it with other substituents. The results indicate that the amino group was not essential for anticonvulsant activity. However its replacement by an aryl ring generally abolished activity while a terminal phenylamino function was better tolerated. Thus both the size of the group and its hydrogen bonding capabilities appear to influence bioactivity. Alteration of the oxygen atom of the semicarbazones by isosteres did not enhance anticonvulsant properties.
