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dc.contributor.author
Simonetti, Sebastián Osvaldo
dc.contributor.author
Larghi, Enrique Leandro
dc.contributor.author
Kaufman, Teodoro Saul
dc.date.available
2018-07-20T16:11:35Z
dc.date.issued
2016-12
dc.identifier.citation
Simonetti, Sebastián Osvaldo; Larghi, Enrique Leandro; Kaufman, Teodoro Saul; The 3,4-dioxygenated 5-hydroxy-4-aryl-quinolin-2(1: H)-one alkaloids. Results of 20 years of research, uncovering a new family of natural products; Royal Society of Chemistry; Natural Product Reports; 33; 12; 12-2016; 1425-1446
dc.identifier.issn
0265-0568
dc.identifier.uri
http://hdl.handle.net/11336/52739
dc.description.abstract
Covering: up to April 2016 Aspergillus and Penicillium are fungal species known to produce a high diversity of secondary metabolites, many of them endowed with interesting bioactivity. The small but steadily growing family of the naturally occurring 5-hydroxy-4-aryl-quinolin-2(1H)-one alkaloids and closely related compounds, which represent the results of various research projects that spanned over 20 years and involved scientists from different continents, are covered here. Emphasis is placed on the isolation and chemical structures of the different compounds, together with their source microorganisms, environmental conditions, country or region of origin, and relevant biological activities. In addition, stereochemical aspects, as well as the proposed biosynthetic pathways for the different members, and the incipient synthetic efforts towards some of the compounds or their key intermediates, are discussed in detail.
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
Natural Products
dc.subject
Organic Synthesis
dc.subject
Quinolones
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Biological Activity
dc.subject.classification
Otras Ciencias Químicas
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Ciencias Químicas
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CIENCIAS NATURALES Y EXACTAS
dc.title
The 3,4-dioxygenated 5-hydroxy-4-aryl-quinolin-2(1: H)-one alkaloids. Results of 20 years of research, uncovering a new family of natural products
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2018-07-18T20:49:32Z
dc.journal.volume
33
dc.journal.number
12
dc.journal.pagination
1425-1446
dc.journal.pais
Reino Unido
dc.journal.ciudad
Cambridge
dc.description.fil
Fil: Simonetti, Sebastián Osvaldo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario. Instituto de Química Rosario. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Química Rosario; Argentina
dc.description.fil
Fil: Larghi, Enrique Leandro. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario. Instituto de Química Rosario. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Química Rosario; Argentina
dc.description.fil
Fil: Kaufman, Teodoro Saul. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario. Instituto de Química Rosario. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Química Rosario; Argentina
dc.journal.title
Natural Product Reports
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/https://dx.doi.org/10.1039/C6NP00064A
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://pubs.rsc.org/en/Content/ArticleLanding/2016/NP/C6NP00064A
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