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dc.contributor.editorSilva, Vera L. M.
dc.contributor.editorSilva, Artur M. S.
dc.date.accessioned2022-11-17T16:22:23Z
dc.date.available2022-11-17T16:22:23Z
dc.date.issued2022
dc.identifierONIX_20221117_9783036554211_6
dc.identifier.urihttps://directory.doabooks.org/handle/20.500.12854/93749
dc.description.abstractPyrazoles and their reduced form, pyrazolines, are considered privileged scaffolds in medicinal chemistry, owing to their noteworthy biological activities, physicochemical properties and occurrence in many low-molecular-weight compounds present in several marketed drugs (e.g., Celebrex® and Viagra®). Pyrazoles are also found in a variety of agrochemicals (fungicides, insecticides, and herbicides) and are versatile compounds for synthetic manipulations. Their challenging chemical structures and properties (mainly tautomerism, with possible implications in their reactivity), and diverse applications, have attracted the attention of many researchers who have developed various synthetic approaches. This reprint presents some examples of the most recent advances in pyrazoles’ chemistry, including synthetic methodologies to access novel pyrazole derivatives, to their functionalization, and studies of their properties and applications in different fields, mainly in medicine and materials science.
dc.languageEnglish
dc.subject.classificationthema EDItEUR::G Reference, Information and Interdisciplinary subjects::GP Research and information: generalen_US
dc.subject.classificationthema EDItEUR::P Mathematics and Science::PN Chemistryen_US
dc.subject.classificationthema EDItEUR::P Mathematics and Science::PN Chemistry::PNN Organic chemistryen_US
dc.subject.otherpyrazolopyridopyridazine dione
dc.subject.otherN-aminopyrazolopyrrolopyridine dione
dc.subject.otherluminol
dc.subject.otherphotoluminescence
dc.subject.otherpyrazole
dc.subject.othercoumarin
dc.subject.otherantimicrobial
dc.subject.otherhydrazone
dc.subject.otherbiofilm
dc.subject.otherStaphylococcus aureus
dc.subject.otherS. epidermidis
dc.subject.otherMRSA
dc.subject.otherpyrazolyl-ureas
dc.subject.otherpyrazole nucleus
dc.subject.otherprotein kinase inhibitors
dc.subject.otheranti-inflammatory agents
dc.subject.otheranticancer agents
dc.subject.otheranti-pathogens agents
dc.subject.othernitrated pyrazoles-based
dc.subject.otherenergetic salts
dc.subject.othersynthesis
dc.subject.otherhigh energy density material
dc.subject.otherinsensitivity
dc.subject.otheramination
dc.subject.other4-halopyrazole
dc.subject.otherBuchwald-Hartwig coupling
dc.subject.otherPd(dba)2
dc.subject.otherCuI mediated coupling
dc.subject.otheraliphatic amine
dc.subject.otherX-ray
dc.subject.otherpyrazolate
dc.subject.othercoinage metals
dc.subject.othermetallacycles
dc.subject.otherM06-2x
dc.subject.otherpyrazolyl-s-triazine
dc.subject.otherFe(III)
dc.subject.otherself-assembly
dc.subject.otherHirshfeld
dc.subject.otherantimicrobial activity
dc.subject.otherpyrazoles
dc.subject.otherstyrylpyrazoles
dc.subject.otherbiological activity
dc.subject.otherorganic synthesis
dc.subject.otherreactivity
dc.subject.otherhomocoupling
dc.subject.otherbipyrazole
dc.subject.othertransition-metal catalysts
dc.subject.othermetal–organic frameworks
dc.subject.other1,3-dipolar cycloadditions
dc.subject.other2,3-dihydropyrazolo[1,2-a]pyrazoles
dc.subject.othercopper-catalyzed azomethine imine-alkyne cycloaddition (CuAIAC)
dc.subject.otherazomethine imines
dc.subject.otherynones
dc.subject.otherbis(pyrazol-1-yl)alkanes
dc.subject.othercarboxylation
dc.subject.otheroxalyl chloride
dc.subject.otherdicarboxylic acids
dc.subject.otheralkylation
dc.subject.othersuperbasic medium
dc.subject.other1,2,4-oxadiazoles
dc.subject.otherspiropyrazolinium compounds
dc.subject.otherin vitro antitubercular screening
dc.subject.otherX-ray diffraction
dc.subject.othermolecular docking
dc.subject.otherpolynuclear
dc.subject.othersilver
dc.subject.othercrystal structure
dc.subject.otherpyrazolate ligand
dc.subject.othercoordination polymer
dc.subject.otherfunctionalization
dc.subject.otherheterocyclic
dc.subject.otherneurodegeneration
dc.subject.otherAlzheimer’s disease
dc.subject.otherParkinson’s disease
dc.subject.otherinhibitor
dc.subject.otherantagonist
dc.subject.otherantitumor scaffold
dc.subject.otherenzymatic inhibitory
dc.subject.otherN-heterocyclic compounds
dc.subject.otherpyrazolo[1,5-a]pyrimidine
dc.subject.otherpyrazolo[1,5-a]pyrimidines
dc.subject.otheraromatic substitution
dc.subject.otherelectrooxidation
dc.subject.otherC–H halogenation
dc.subject.otherC–H thiocyanation
dc.subject.otherN–N coupling
dc.subject.othercyclic voltammetry
dc.subject.othern/a
dc.titleRecent Advances in the Synthesis, Functionalization and Applications of Pyrazole-Type Compounds I
dc.typebook
oapen.identifier.doi10.3390/books978-3-0365-5421-1
oapen.relation.isPublishedBy46cabcaa-dd94-4bfe-87b4-55023c1b36d0
oapen.relation.isbn9783036554211
oapen.relation.isbn9783036554228
oapen.pages400
oapen.place.publicationBasel


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