The synthesis of a series of 2-methyl-7-trichloromethylpyrazolo[1,5-a]pyrimidines from the cyclocondensation reaction of 3-amino-5-methylpyrazole with 1,1,1-trichloro-4- alkoxyalk-3-en-2-ones [CCl3C(O)CH=C(R1)OR where R1 ...

A flow injection (FI) system, which is coupled to an atomic absorption spectrometer, is proposed for organic and inorganic mercury speciation. The FI system consists basically of three three way-solenoid valves, a gas/liquid ...

Seven new compounds involving the phenylseleninato ligand and alkaline and alkaline earth metals were obtained in this work: poly-phenylseleninato lithium(I) (1), catena-polybis(aqua)-phenylseleninato sodium(I) (2), ...

This work describes the synthesis of a new series of 2-[3-alkyl(aryl/heteroaryl)-5-trihalomethyl-5-hydroxy-4,5-dihydro-1H-pyrazol-1-il]-5-[3-alkyl(aryl/heteroaryl)-5-trihalomethyl-5-hydroxy-4,5-dihydro-1H-pyrazol-1-il-1- ...

This work presents a study of the N-alkylation reactions of 4- (trichloromethyl)pyrimidin-2(1H)-one(2), 5-bromo-4-methoxy-4-(trichloromethyl)-3,4-dihydropyrimidin-2-(1H)-one (7), 4-methoxy-4-(trichloromethyl)-3,4-dihydro ...

The present dissertation initially describes methodologies for the synthesis of five 3-(trifluoromethyl)-3,3a-dihydrospiro[chromeno[4,3-c]isoxazole-4,1'-cycloalkan]-3-ols (7) in 65 – 84 % yields, where the spirocarbocyclic ...

Compounds featuring triazenidic units constitute a versatile class of molecules for the preparation of new inorganic complexes with broad applications that include cancer therapy such as leukemia treatment. Gold-triazenide ...

In the following work, a range of 1,3,4-oxadiazles 2,5-disubstituted 3 was prepared, using a one pot approach, from L-amino acids 1(a-e) and 2-benzoylhydrazides, using POCl3 as dehydrating agent. The study involved the ...

The current work reports the incorporation of 4-thiazolidinones to oxadiazolic ring by a simple and effective methodology. Five species of thiazolidinones were synthesized by three component condensation reaction of glycine ...

The present work report the synthesis of β-chalcogen amino compounds derived from L-aminoacids. The desired products were obtained in a short reaction time, with high yields using a simple and environmentally friendly ...