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dc.contributor.author
Orelli, Liliana Raquel
dc.contributor.author
Bisceglia, Juan Angel
dc.contributor.author
Gruber, Nadia
dc.contributor.author
Díaz, Jimena Estela
dc.contributor.author
Mollo, María Cruz
dc.date.available
2022-02-11T16:29:29Z
dc.date.issued
2020
dc.identifier.citation
Orelli, Liliana Raquel; Bisceglia, Juan Angel; Gruber, Nadia; Díaz, Jimena Estela; Mollo, María Cruz; Recent applications of microwave assisted cyclizations promoted by polyphosphoric acid esters to the synthesis of nitrogen heterocycles; Wiley Blackwell Publishing, Inc; 2; 2020; 631-666
dc.identifier.isbn
9781119708841
dc.identifier.uri
http://hdl.handle.net/11336/151888
dc.description.abstract
Polyphosphoric acid (PPA) esters PPE (ethyl polyphosphate) and PPSE (trimethylsilyl polyphosphate) are mild reagents of the Lewis acid type with a high dehydrating power due to their ability to react irreversibly with water.They are used mainly to conduct condensation reactions in which they bond to the oxygen atom present in alcohols, carbonyls and carboxylic acid derivatives generating electrophilic carbon species.The introduction describes the preparation, structure and applications of PPE and PPSE in the construction of heterocyclic moieties by both C-C and C-heteroatom bond formation. The main body of this chapter is devoted to the applications of the reagents to the synthesis of nitrogen heterocycles under microwave irradiation developed by our group.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
Wiley Blackwell Publishing, Inc
dc.rights
info:eu-repo/semantics/restrictedAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
PPE
dc.subject
PPSE
dc.subject
NITROGEN HETEROCYCLES
dc.subject
MICROWAVES
dc.subject.classification
Química Orgánica
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Ciencias Químicas
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CIENCIAS NATURALES Y EXACTAS
dc.title
Recent applications of microwave assisted cyclizations promoted by polyphosphoric acid esters to the synthesis of nitrogen heterocycles
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
2021-10-18T15:44:13Z
dc.journal.volume
2
dc.journal.pagination
631-666
dc.journal.pais
Estados Unidos
dc.journal.ciudad
Hoboken
dc.description.fil
Fil: Orelli, Liliana Raquel. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Química Orgánica; Argentina
dc.description.fil
Fil: Bisceglia, Juan Angel. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Química Orgánica; Argentina
dc.description.fil
Fil: Gruber, Nadia. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Química Orgánica; Argentina
dc.description.fil
Fil: Díaz, Jimena Estela. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Química Orgánica; Argentina
dc.description.fil
Fil: Mollo, María Cruz. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Química Orgánica; Argentina
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://doi.org/10.1002/9781119708841.ch20
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/book/10.1002/9781119708841
dc.conicet.paginas
900
dc.source.titulo
Synthetic Approaches to Nonaromatic Nitrogen Heterocycles
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