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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  
dc.subject.classification
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