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dc.contributor.author
Yerien, Damián Emilio  
dc.contributor.author
Bonesi, Sergio Mauricio  
dc.contributor.author
Postigo, Jose Alberto  
dc.date.available
2017-06-08T15:36:30Z  
dc.date.issued
2016-05  
dc.identifier.citation
Yerien, Damián Emilio; Bonesi, Sergio Mauricio; Postigo, Jose Alberto; Fluorination methods in drug discovery; Royal Society Of Chemistry; Organic & Biomolecular Chemistry; 14; 36; 5-2016; 8398-8427  
dc.identifier.issn
1477-0520  
dc.identifier.uri
http://hdl.handle.net/11336/17770  
dc.description.abstract
Fluorination reactions of medicinal and biologically-active compounds will be discussed. Late stage fluorination strategies of medicinal targets have recently attracted considerable attention on account of the influence that the fluorine atom can impart to targets of medicinal importance, such as a modulation of lipophilicity, electronegativity, basicity and bioavailability, this latter as a consequence of membrane permeability. Therefore, the recourse to late-stage fluorine substitution on compounds with already known and relevant biological activity can provide the pharmaceutical industry with new leads with improved medicinal properties. The fluorination strategies will take into account different fluorinating reagents, nucleophilic, electrophilic and of radical nature. Diverse families of organic compounds such as (hetero)aromatic rings, and aliphatic substrates (sp3 , sp 2 , and sp carbon atoms) will be studied in late-stage fluorination reaction strategies.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Royal Society Of Chemistry  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
Fluorination  
dc.subject
Drug Discovery  
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Biological Targets  
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Medicinal Compounds  
dc.subject.classification
Química Orgánica  
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Ciencias Químicas  
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CIENCIAS NATURALES Y EXACTAS  
dc.title
Fluorination methods in drug discovery  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2017-06-07T20:46:45Z  
dc.journal.volume
14  
dc.journal.number
36  
dc.journal.pagination
8398-8427  
dc.journal.pais
Reino Unido  
dc.journal.ciudad
Londres  
dc.description.fil
Fil: Yerien, Damián Emilio. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Química Orgánica; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina  
dc.description.fil
Fil: Bonesi, Sergio Mauricio. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Centro de Investigaciones en Hidratos de Carbono. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Centro de Investigaciones en Hidratos de Carbono; Argentina  
dc.description.fil
Fil: Postigo, Jose Alberto. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Química Orgánica; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina  
dc.journal.title
Organic & Biomolecular Chemistry  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1039/C6OB00764C  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://pubs.rsc.org/en/Content/ArticleLanding/2016/OB/C6OB00764C#!divAbstract