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dc.contributor.author
Rossi, Roberto Arturo
dc.contributor.author
Buden, Maria Eugenia
dc.contributor.author
Guastavino, Javier Fernando
dc.contributor.other
Mortier, Jacques
dc.date.available
2024-10-14T10:47:27Z
dc.date.issued
2015
dc.identifier.citation
Rossi, Roberto Arturo; Buden, Maria Eugenia; Guastavino, Javier Fernando; Homolytic Aromatic Substitution; John Wiley & Sons; 2; 2015; 219-242
dc.identifier.isbn
9781118752012
dc.identifier.uri
http://hdl.handle.net/11336/245918
dc.description.abstract
Homolytic aromatic substitution (HAS) encompasses a wide range of synthetic transformations based on inter- and intramolecular additions of radicals to arenes. This chapter is intended to provide a description of important aspects and recent advances of these reactions including the principal mechanisms and the synthetic protocols used. An overview of selected examples are shown, which can be used as guides for a planned transformation. The chapter has been organized according to the different routes to generate the intermediate radicals. In the first one, the radicals are formed by homolytic cleavage processes (thermolysis and photolysis). The second route involves the use of peroxides or free radical initiator with tin hydrides and silanes. Finally, the third route involves redox reactions, where radicals can also be generated either by reduction or oxidation of an appropriate precursor. Also, the base-promoted electron transfer to induce the HAS is presented. In each of the procedures, various examples have been selected with the intent of showing which reaction is a suitable alternative to gain access to complex molecules, which makes these processes a powerful synthetic tool.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
John Wiley & Sons
dc.rights
info:eu-repo/semantics/restrictedAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
ARYLATION REACTIONS
dc.subject
BASE-PROMOTED HOMOLYTIC AROMATIC SUBSTITUTION
dc.subject
HOMOLYTIC AROMATIC SUBSTITUTION
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HOMOLYTIC CLEAVAGE PROCESSES
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PHOTOLYSIS
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REDOX REACTIONS
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SILICON HYDRIDES
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THERMOLYSIS
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TIN HYDRIDES
dc.subject.classification
Química Orgánica
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Ciencias Químicas
dc.subject.classification
CIENCIAS NATURALES Y EXACTAS
dc.title
Homolytic Aromatic Substitution
dc.type
info:eu-repo/semantics/publishedVersion
dc.type
info:eu-repo/semantics/bookPart
dc.type
info:ar-repo/semantics/parte de libro
dc.date.updated
2024-04-29T17:34:36Z
dc.journal.volume
2
dc.journal.pagination
219-242
dc.journal.pais
Estados Unidos
dc.journal.ciudad
Hoboken
dc.description.fil
Fil: Rossi, Roberto Arturo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina
dc.description.fil
Fil: Buden, Maria Eugenia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina
dc.description.fil
Fil: Guastavino, Javier Fernando. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Desarrollo Tecnológico para la Industria Química. Universidad Nacional del Litoral. Instituto de Desarrollo Tecnológico para la Industria Química; Argentina
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/10.1002/9781118754887.ch9
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1002/9781118754887.ch9
dc.conicet.paginas
992
dc.source.titulo
Arene Chemistry: Reaction Mechanisms and Methods for Aromatic Compounds
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