Chlorine in an Organic Molecule, a Universal Promoter—Workhorse—Of Reactions

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dc.contributor.authorMąkosza, Mieczysław
dc.contributor.authorFedoryński, Michał
dc.contributor.editorDembinski, Roman
dc.contributor.organizationInstitute of Organic Chemistry, Polish Academy of Sciences
dc.contributor.organizationFaculty of Chemistry, Warsaw University of Technology
dc.date.accessioned2024-09-18T14:23:52Z
dc.date.available2024-09-18T14:23:52Z
dc.date.issued2023
dc.description.abstractDue to the electronic configuration of the atom and charge of the nucleus, the chlorine in organic molecules can exert a variety of effects. It can depart as a chloride anion in the process of substitution and elimination, facilitates the abstraction of protons and stabilizes generated carbanions, exerts moderate stabilizing effect of carbenes, carbocations and radicals. There are frequent cases where chlorine substituent promotes more than one transformation. These rich effects of chlorine substituent will be illustrated by examples of our work.en
dc.identifier.citationMolecules 2023, 28, 7957 ; https://doi.org/10.3390/molecules28247957
dc.identifier.doi10.3390/molecules28247957
dc.identifier.issn1420-3049
dc.identifier.urihttps://open.icm.edu.pl/handle/123456789/24859
dc.language.isoen
dc.publisherMDPI
dc.rightsUznanie autorstwa 4.0 Międzynarodoween
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceMolecules
dc.subjectphase transfer catalysisen
dc.subjectγ-halocarbanionsen
dc.subjectdichlorocarbeneen
dc.subjectvicarious nucleophilic substitutionen
dc.subjectnucleophilic substitution of chlorineen
dc.subjectbase induced β-eliminationen
dc.subjectα-halocarbanionsen
dc.subjectDarzens reactionen
dc.subjectchlorine as electrophilic centeren
dc.titleChlorine in an Organic Molecule, a Universal Promoter—Workhorse—Of Reactionsen
dc.typearticle
dc.type.versionpublishedVersion
person.identifier.orcidMąkosza, Mieczysław [0000-0001-9091-7792]
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