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The asymmetric Petasis borono-Mannich reaction : insights on the last 15 years

datacite.subject.fosCiências Naturais::Ciências Químicas
dc.contributor.authorMarques, Carolina
dc.contributor.authorBrandão, Pedro
dc.date.accessioned2026-03-16T12:55:24Z
dc.date.available2026-03-16T12:55:24Z
dc.date.issued2023-06
dc.description.abstractThe Petasis borono-Mannich reaction, commonly described as the Petasis reaction, was one of the latest famous multicomponent reactions described in the literature. Currently celebrating its 30th anniversary since it was first reported by Petasis and Akritopoulou in 1993, this reaction has emerged as a powerful tool for the synthesis of biologically relevant molecules (such as substituted amines or amino acids), among others. This three-component catalyst-free reaction (the classic model), involving the coupling of an aldehyde, an amine, and a boronic acid, enables the synthesis of polysubstituted amine-containing molecules. Several accounts regarding the catalyst-free version using different carbonyl, amine, and boron-type components have been reported thus far. In contrast, the asymmetric version is still in its infancy since it was first reported in 2007. In this work, we aim to review the asymmetric versions of the Petasis reaction reported over the last 15 years, considering the chiral pool approach (asymmetric induction by one reaction component) and the use of catalysts (organocatalysts, transition-metal catalysts, and others) to access enantiomeric and diastereomeric pure amino-derivatives. Insights regarding the catalyzed Petasis reaction and consequent sustainable synthesis will be highlighted.eng
dc.identifier.citationMarques C, Brandão P. The Asymmetric Petasis Borono-Mannich Reaction: Insights on the Last 15 Years. Catalysts. 2023; 13(6):1022. https://doi.org/10.3390/catal13061022
dc.identifier.doi10.3390/catal13061022
dc.identifier.issn2073-4344
dc.identifier.urihttp://hdl.handle.net/10400.26/62202
dc.language.isoeng
dc.peerreviewedyes
dc.publisherMDPI
dc.relation.hasversionhttps://doi.org/10.3390/catal13061022
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectPetasis borono-Mannich reaction
dc.subjectasymmetric
dc.subjectenantioselective
dc.subjectdiastereoselective
dc.subjectorganocatalyst
dc.subjectmulticomponent reaction
dc.titleThe asymmetric Petasis borono-Mannich reaction : insights on the last 15 yearseng
dc.typecontribution to journal
dspace.entity.typePublication
oaire.citation.issue6
oaire.citation.startPage1022
oaire.citation.titleCatalysts
oaire.citation.volume13
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85

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