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Arylpyridines: A Review from Selective Synthesis to Atropisomerism

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dc.abstract.enMultiply arylated heterocycles are interesting structures with highly useful functions and fascinating optoelectronic and biological properties. Pyridines are an important class of compounds, playing a role in various fields of chemistry. When the pyridine ring is connected to other aromatic systems, novel stereochemical outcomes may arise. This work summarizes different methodologies applied for the synthesis of substituted arylpyridine derivatives and summarizes stereochemical phenomena resulting from atropisomerism present in certain arylated pyridines.
dc.affiliationUniwersytet Warszawski
dc.contributor.authorPomarański, Piotr
dc.contributor.authorCzarnocki, Zbigniew
dc.date.accessioned2024-01-24T16:56:40Z
dc.date.available2024-01-24T16:56:40Z
dc.date.issued2019
dc.description.financeNie dotyczy
dc.description.number3
dc.description.volume51
dc.identifier.doi10.1055/S-0037-1611365
dc.identifier.issn0039-7881
dc.identifier.urihttps://repozytorium.uw.edu.pl//handle/item/101175
dc.languageeng
dc.pbn.affiliationchemical sciences
dc.relation.ispartofSynthesis
dc.relation.pages587-611
dc.rightsClosedAccess
dc.sciencecloudnosend
dc.subject.enpyridine derivatives
dc.subject.enheterocyclic compounds
dc.subject.enstereochemistry
dc.subject.enatropisomerism
dc.subject.enSuzuki–Miyaura reaction
dc.titleArylpyridines: A Review from Selective Synthesis to Atropisomerism
dc.typeJournalArticle
dspace.entity.typePublication