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dc.contributor.author
Della Rosa, Claudia Daniela
dc.contributor.author
Kneeteman, Maria Nelida
dc.contributor.author
Mancini, Pedro Maximo Emilio
dc.date.available
2020-04-16T19:20:28Z
dc.date.issued
2005-12
dc.identifier.citation
Della Rosa, Claudia Daniela; Kneeteman, Maria Nelida; Mancini, Pedro Maximo Emilio; 2-Nitrofurans as dienophiles in Diels–Alder reactions; Pergamon-Elsevier Science Ltd; Tetrahedron Letters; 46; 50; 12-2005; 8711-8714
dc.identifier.issn
0040-4039
dc.identifier.uri
http://hdl.handle.net/11336/102782
dc.description.abstract
2-Nitrofuran derivatives are studied in Diels-Alder reactions under thermal conditions. In contrast to 2-acilfurans, they proved to be efficient dienophiles.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
Pergamon-Elsevier Science Ltd
dc.rights
info:eu-repo/semantics/openAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
DIELS-ALDER
dc.subject
DIENOPHILES
dc.subject
NITROFURANS
dc.subject.classification
Química Orgánica
dc.subject.classification
Ciencias Químicas
dc.subject.classification
CIENCIAS NATURALES Y EXACTAS
dc.title
2-Nitrofurans as dienophiles in Diels–Alder reactions
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2020-04-13T13:13:57Z
dc.journal.volume
46
dc.journal.number
50
dc.journal.pagination
8711-8714
dc.journal.pais
Países Bajos
dc.journal.ciudad
Amsterdam
dc.description.fil
Fil: Della Rosa, Claudia Daniela. Universidad Nacional del Litoral; Argentina
dc.description.fil
Fil: Kneeteman, Maria Nelida. Universidad Nacional del Litoral; Argentina
dc.description.fil
Fil: Mancini, Pedro Maximo Emilio. Universidad Nacional del Litoral; Argentina
dc.journal.title
Tetrahedron Letters
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.tetlet.2005.10.042
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