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dc.contributor.author
Larghi, Enrique Leandro
dc.contributor.author
Bracca, Andrea Beatriz Juana
dc.contributor.author
Simonetti, Sebastián Osvaldo
dc.contributor.author
Kaufman, Teodoro Saul
dc.date.available
2025-02-25T13:33:10Z
dc.date.issued
2023-12
dc.identifier.citation
Larghi, Enrique Leandro; Bracca, Andrea Beatriz Juana; Simonetti, Sebastián Osvaldo; Kaufman, Teodoro Saul; Recent developments in the total synthesis of natural products using the Ugi multicomponent reactions as the key strategy; Royal Society of Chemistry; Organic & Biomolecular Chemistry; 22; 3; 12-2023; 429-465
dc.identifier.issn
1477-0520
dc.identifier.uri
http://hdl.handle.net/11336/255151
dc.description.abstract
The total syntheses of selected natural products using different versions of the Ugi multicomponent reaction is reviewed on a case-by-case basis. The revision covers the period 2008-2023 and includes detailed descriptions of the synthetic sequences, the use of state-of-the-art chemical reagents and strategies, as well as the advantages and limitations of the transformation and some remedial solutions. Relevant data on the isolation and bioactivity of the different natural targets are also briefly provided. The examples clearly evidence the strategic importance of this transformation and its key role in the modern natural products synthetic chemistry toolbox. This methodology proved to be a valuable means for easily building molecular complexity and efficiently delivering step-economic syntheses even of intricate structures, with a promising future.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
Royal Society of Chemistry
dc.rights
info:eu-repo/semantics/restrictedAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
MULTICOMPONENT REACTION
dc.subject
NATURAL PRODUCTS
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TOTAL SYNTHESIS
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BIOLOGICAL ACTIVITY
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Química Orgánica
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Ciencias Químicas
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CIENCIAS NATURALES Y EXACTAS
dc.title
Recent developments in the total synthesis of natural products using the Ugi multicomponent reactions as the key strategy
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2024-11-27T09:47:21Z
dc.journal.volume
22
dc.journal.number
3
dc.journal.pagination
429-465
dc.journal.pais
Reino Unido
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: Bracca, Andrea Beatriz Juana. 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: 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: 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
Organic & Biomolecular Chemistry
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://pubs.rsc.org/en/content/articlelanding/2024/ob/d3ob01837g/unauth
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1039/D3OB01837G
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