Results 1 to 10 of about 10,572 (203)

Nitroreductase-triggered indazole formation [PDF]

open access: yesNature Communications
Biocatalysis contributes significantly to the development of more sustainable synthetic pathways by using mild reaction conditions and water as a solvent.
Henrik Terholsen   +5 more
doaj   +3 more sources

Synthesis, Characterization, Antimicrobial Activity and Molecular Modeling Studies of Novel Indazole-Benzimidazole Hybrids [PDF]

open access: yesAntibiotics
Background/Objectives: In this work, a series of six new indazole-benzimidazole hybrids (M1–M6) were designed, synthesized, and fully characterized. The design of these compounds was based on the combination of two pharmacophoric units, indazole and ...
Redouane Er-raqioui   +14 more
doaj   +2 more sources

Facile indazole-endowed thiadiazole hybrid derivatives as antibacterial, anti-diabetic and thymidine phosphorylase inhibitors: An insight to experimental, in-vitro biological potential and computational approaches [PDF]

open access: yesSaudi Pharmaceutical Journal
In this study, a series of newly synthesized indazole-based thiadiazole hybrid derivatives (1–13) were successfully synthesized from indazole-based thiosemicarbazides starting from the 5-methyl-1H-indazole-3-carboxylic acid.
Sabeen Arshad   +6 more
doaj   +2 more sources

Crystal structure of 2-[2-(2,5-dichlorobenzyloxy)-2-(furan-2-yl)ethyl]-2H-indazole

open access: yesActa Crystallographica Section E: Crystallographic Communications, 2016
In the title compound, C20H16Cl2N2O2, the indazole ring system is approximately planar [maximum deviation = 0.033 (1) Å], its mean plane is oriented at dihedral angles of 25.04 (4) and 5.10 (4)° to the furan and benzene rings, respectively.
Özden Özel Güven   +4 more
doaj   +4 more sources

Indazole: Photoleitfähigkeit und Oxidationspotentiale

open access: yesCHIMIA, 1988
In sensitized electrophotographic layers, excellent charge transport properties are exhibited by 2-(p-aminophenyl)indazoles (1). Corresponding 2-aminoindazoles (2) are ineffective.
Bernhard Albert   +2 more
doaj   +2 more sources

Synthesis, Antiprotozoal Activity, and Cheminformatic Analysis of 2-Phenyl-2H-Indazole Derivatives

open access: yesMolecules, 2021
Indazole is an important scaffold in medicinal chemistry. At present, the progress on synthetic methodologies has allowed the preparation of several new indazole derivatives with interesting pharmacological properties.
Karen Rodríguez-Villar   +9 more
doaj   +1 more source

(7E)-3-(4-Methoxyphenyl)-7-[(4-methoxyphenyl)methylidene]-4,5,6,7-tetrahydro-3aH-indazole

open access: yesMolbank, 2020
Indazole derivatives are well known to have various pharmacological activities. We synthesized a novel derivative of indazole, namely (7E)-3-(4-methoxyphenyl)-7-[(4-methoxyphenyl)methylidene]-4,5,6,7-tetrahydro-3aH-indazole by condensation reaction ...
Hariyanti Hariyanti   +3 more
doaj   +1 more source

Regioselective N-alkylation of the 1H-indazole scaffold; ring substituent and N-alkylating reagent effects on regioisomeric distribution

open access: yesBeilstein Journal of Organic Chemistry, 2021
The indazole scaffold represents a promising pharmacophore, commonly incorporated in a variety of therapeutic drugs. Although indazole-containing drugs are frequently marketed as the corresponding N-alkyl 1H- or 2H-indazole derivative, the efficient ...
Ryan M. Alam, John J. Keating
doaj   +1 more source

Methyl 1-(4-fluorobenzyl)-1H-indazole-3-carboxylate

open access: yesIUCrData, 2023
The title compound, C16H13FN2O2, was synthesized by nucleophilic substitution of the indazole N—H hydrogen atom of methyl 1H-indazole-3-carboxylate with 1-(bromomethyl)-4-fluorobenzene. In the crystal, some hydrogen-bond-like interactions are observed.
Takahiro Doi, Takayuki Sakai
doaj   +1 more source

Davis-Beirut reaction: route to thiazolo-, thiazino-, and thiazepino-2H-indazoles. [PDF]

open access: yes, 2014
Methods for the construction of thiazolo-, thiazino-, and thiazepino-2H-indazoles from o-nitrobenzaldehydes or o-nitrobenzyl bromides and S-trityl-protected 1°-aminothioalkanes are reported.
Farber, Kelli M   +2 more
core   +2 more sources

Home - About - Disclaimer - Privacy