Results 51 to 60 of about 7,519 (213)
Several new N-phenyl-1H-indazole-1-carboxamides 1c–h and 4l,m were prepared by reacting phenyl isocyanate derivatives 3a,b with 3-amino-1H-indazole derivatives 2c,e,g or 1H-indazole 2l respectively.
Rosaria Maria Pipitone +21 more
core +1 more source
1-(4-Methylphenylsulfonyl)-5,6-dinitro-1H-indazole
In the title compound, C14H10N4O6S, the indazole ring system is almost perpendicular to the tosyl ring, as indicated by the dihedral angle of 89.40 (9)° between their planes.
Bassou Oulemda +4 more
doaj +1 more source
ABSTRACT We present chemical kinetic rate constants for the cis to trans isomerisation or rotamerization of monomeric seleno‐, thio‐, and formic acids and that of three of their dimeric species, based on variational transition state theory and multidimensional tunneling calculations in the gas‐phase, from 10 K to 300 K. These provide, firstly, reliable
Judith Wurmel, John M. Simmie
wiley +1 more source
The reaction of 2,4-disubstituted thiosemicarbazides with 2,3,5,6-tetrachloro-1,4-benzo-quinone gave 2-aryl-5,6-dichloro-3-(substituted imino)-2,3-dihydro-1 H-indazole-4,7-diones in 57–66% yield together with smaller amounts of 2-aryl-3-(substituted ...
Mamdouh A. Mohamed +2 more
core +1 more source
Discrete and polymeric Cu(II) complexes featuring substituted indazole ligands: their synthesis and structural chemistry [PDF]
Reported here are the syntheses of four indazole-based ligands and the structural characterisation of four Cu(II) complexes derived from them. The ligands 1-(2-pyridyl)-1H-indazole, L1, and 2-(2-pyridyl)-2Hindazole, L2, have been characterised by ...
Hawes, C.S. +3 more
core +1 more source
The monoamine oxidase inhibition properties of indazole derivatives
The monoamine oxidase (MAO) enzymes are important catalysts of the metabolism of biogenic and dietary amines in the central and peripheral nervous systems.
Mohau G. Mashishi +3 more
doaj +1 more source
A Tale of Two Heterocycles: How Oxygen and Sulfur Shape Divergent Kemp Reactivity
Like benzisoxazoles, benzisothiazoles also undergo Kemp elimination, with rates accelerated by aprotic polar solvents and electron‐withdrawing groups. Oxygen‐containing heterocycles exhibit more localized negative charges than sulfur analogs, resulting in a more pronounced catalytic response to these environmental factors. ABSTRACT The Kemp elimination
Ella R. Jennings +5 more
wiley +1 more source
Synthesis and evaluation of antibacterial activity of novel 3-methyl-1H-indazole derivatives
Aim of the study was designed to synthesize and evaluate antibacterial activity of novel heterocyclic compounds, 3-methyl-1H-indazole derivatives. The heterocyclic compounds, 3-methyl-1H-indazole derivatives (1a-1d and 2a-2d) were synthesized; all of ...
Farrukh Shaikh +4 more
doaj +1 more source
Ethyl 2-(6-nitro-1H-indazol-1-yl)acetate
The asymmetric unit of the title compound, C11H11N3O4, comprises two independent molecules, both of which display positional disorder of their ethyl chains in 0.868 (4):0.132 (4) and 0.839 (4):0.161 (4) ratios. The packing is directed by a combination of
Mohamed Mokhtar Mohamed Abdelahi +4 more
doaj +1 more source
A series of 12 novel fused [6,6] saturated and unsaturated nitrogen bicycles is synthesized in three to five steps and expands the CRAFT library's fragment space. A 2,6‐naphthyridin‐3‐ol core replaces the dihydroquinolinone scaffold of aripiprazole, a scaffold‐hopping strategy.
Temitayo Omowumi Alegbejo Price +12 more
wiley +1 more source

