Results 31 to 40 of about 92,195 (127)
2‐Aryl‐3‐phenylamino‐4,5‐dihydro‐2H‐benz[g]indazoles with Analgesic Activity.
A series of 2-aryl-3-phenylamino-4,5-dihydro-2H-benz[g]indazoles was synthesized and tested for antiarrhythmic, local anaesthetic and analgesic activity.
W. FILIPPELLI +17 more
core +1 more source
The development of a novel selective synthesis of 3-amino-2H-indazoles from readily available 2-halobenzonitriles is presented. The reaction proceeds through a domino reaction sequence, consisting of a regioselective palladium-catalyzed coupling of ...
Lindemann, P. +6 more
core +1 more source
A multicatalytic strategy based on the simple combination of metal‐organic frameworks (MOFs) and organocatalysts is able to mediate challenging aerobic oxidation reactions. The use of earth‐abundant MOFs and commercially available (hydro)quinone co‐catalysts greatly simplify the generation of powerful multicatalytic systems, opening the door for the ...
Juan Camilo Arango‐Daza +5 more
wiley +2 more sources
Monosubstituted N‐arylhydroxylamines represent a unique subclass of hydroxylamines that act as pivotal intermediates in redox transformations and as versatile platforms for further synthetic transformations. They serve as key building blocks in the synthesis of architecturally complex heterocycles and other valuable organic compounds.
Michael G. Kallitsakis +2 more
wiley +1 more source
Organophosphorus-mediated N-N bond formation: facile access to 3-amino-2H-indazoles
A convenient and efficient strategy has been devised to access 3-amino-2H-indazole derivatives in two steps from readily available starting materials.
Nazare, M. +3 more
core +1 more source
Mechanistic and Reactivity Insights into Diboron‐Mediated NN and NN Bond Scission
This review highlights the emerging ability of diboron reagents to cleave both π‐bonded (N=N) and σ‐bonded (N—N) nitrogen–nitrogen linkages, integrating mechanistic understanding with recent synthetic applications. Diboron reagents have emerged as versatile reducing agents capable of transforming a broad range of functional groups through pathways like
Raúl Valderrama‐Callejón +2 more
wiley +1 more source
4F ABUTINACA maintains stable intravenous self‐administration at low doses in male rats, supporting its high abuse potential. Chronic exposure to 4F‐ABUTINACA induces persistent anxiety‐like behaviors and is associated with region‐specific neurotoxicity in the hippocampus, prefrontal cortex and nucleus accumbens, alongside dysregulation of the BDNF ...
Baobao Shi +10 more
wiley +1 more source
Cu/Pd cooperatively catalyzed tandem C–N and C–P bond formation: access to phosphorated 2H-indazoles
An unprecedented Cu/Pd cooperatively catalyzed tandem C–N/C–P bond formation reaction for the synthesis of phosphorated 2H-indazoles has been developed.
Aijun Lin +4 more
core +1 more source
A simple and efficient electrochemical method that utilizes modulation of the cell voltage to cause structural alterations in 2H-indazole is introduced. This method enables the C-3 acyloxylation of 2H-indazole and promotes the transfer of the acyl group ...
Neetu Kumari +11 more
core +2 more sources
Electrophilic Iodination of Heterocyclic Compounds. Recent Advances 2008–2025: Part II
Electrophilic iodination using molecular iodine and iodide sources represents an efficient approach for accessing valuable iodinated organic compounds. This review highlights recent advances in the iodination of heterocyclic compounds from 2008 to 2025, emphasizing the role of heteroaryl iodides as important synthetic intermediates for biologically ...
Njomza Ajvazi, Stojan Stavber
wiley +1 more source

