Among the methods used for synthesis of functionalized heterocyclic compounds, photochemistry has gained immense popularity due to reactivity intermediates in photoinduced reactions. In this study, we report on effect diaryl disulfides as hydrogen atom transfer catalysts transformations pyrazolo[1,2-a]pyrazolones. After excitation with visible light, these compounds are susceptible C–N bond cle...

An alternative synthesis of cycloalkyl-substituted CPA catalysts is reported. A Negishi coupling offers improved yields and purity the necessary 1,3,5-tri(cycloalkyl)benzenes. Limitations in use commercial organozinc reagents have been identified a robust procedure for preparation these detailed. Similarly, key Kumada also provided. The route demonstrated by three different tri(cycloalkyl)aryl-...

1-[(N-acetyl)2,3-dichloroanilinomalonyl]3,5-dimethyl-4-(unsubstituted/substituted phenylazo) pyrazoles have been synthesised in 34 to 65% yield, by the reaction of 2,4-diketo-3(unsubstituted/substituted phenylazo) pentane with Ethyl-2-[(N-acetyl)2,3-dichloroanilido] acetohydrazide. Pyrazoles are brown and yellow colour solids, having high melting points. Identity of products has been establishe...

The structures of six inhibitors of prolyl hydroxylase, fibrostatins A, B, C, D, E and F produced by a strain of Streptomyces, were deduced to be 1, 2, 3, 4, 5 and 6, respectively, from chemical and spectroscopic evidence, especially from extensive 13C NMR studies including selective decoupling and low power selective decoupling experiments monitored by 13C-1H long-range couplings. These compou...

Pyrazoles have been studied for over a century as an important class of heterocyclic compounds and continue to attract considerable interest due to the broad range of biological activities they possess. The incorporation of the essential structural features of pyrazoles with a ferrocene moiety could provide new derivatives with unexpected and/or enhanced biological activities since several ferr...

A novel one-pot synthesis of tri-substituted purines and the discovery of purine analogues with trypanocidal activity are reported. The reaction is initiated by a metal-free oxidative coupling of primary alkoxides and diaminopyrimidines with Schiff base formation and subsequent annulation in the presence of large N,N-dimethylamides (e.g. N,N-dimethylpropanamide or larger). This synthetic route ...

A three-component reaction has been developed that allows the regioselective synthesis of thieno[2,3-c]pyrroles. The reaction is based on the ability of 2-acetyl-3-thiophenecarboxaldehyde to react with amine and thiol nucleophiles to produce the corresponding tri-substituted thieno[2,3-c]pyrroles, with water as the only by-product. The developed reaction expands the range of synthetically acces...

New resveratrol (trans-3,4',5-trihydroxystilbene) analogs were synthesized and screened for their in vitro cancer chemopreventive potential using various bioassays relevant for the prevention of carcinogenesis in humans: two assays to detect modulators of carcinogen metabolism (Cyp1A inhibition; determination of NAD(P)H/quinone reductase (QR) activity), three assays to identify radical scavengi...

Background: Pyrazole is a simple aromatic ring an organic compound of the heterocyclic series that characterized five-membered ring structure which comprises located adjacent two nitrogen atoms and three carbon atoms. In recent years interest in the pyrazole chemistry excessively has increased due to many a wide range of properties. Because they have a wide range of specific properties such as ...