Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/107438
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dc.contributor.authorAlves, Nuno Guerreiro-
dc.contributor.authorAlves, Américo J. S.-
dc.contributor.authorSoares, Maria I. L.-
dc.contributor.authorPinho e Melo, Teresa M. V. D.-
dc.date.accessioned2023-07-12T08:34:32Z-
dc.date.available2023-07-12T08:34:32Z-
dc.date.issued2021-
dc.identifier.issn1615-4150pt
dc.identifier.issn1615-4169pt
dc.identifier.urihttps://hdl.handle.net/10316/107438-
dc.description.abstractSpirocyclic molecules are widely recognized for their complex three-dimensional features and structural rigidity. Among this class of molecules, the spiro-lactams subclass stands out, being extensively explored due to its bioactivity and utility in a variety of scientific fields such as drug design and organic synthesis. Given the recognition of spirocyclic lactams’ broad potential, several efforts have been engaged on the pursuit of new synthetic strategies towards these molecules. The present review gathers advances on the synthesis of both spiro- β-lactams (spiroazetidin-2-ones) and spiro-δ-lactams (spiropiperidon-2-ones) reported since 2015. The work is divided into two distinct parts, each one dedicated to one of these types of spiro-lactam, with the approach used for building the spirocyclic system being extensively discussed, according to the method’s scope, efficiency, selectivity, and reaction mechanism.pt
dc.language.isoengpt
dc.publisherWiley Online Librarypt
dc.relationinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB/00313/2020/PT/Coimbra Chemistry Centerpt
dc.relationinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDP/00313/2020/PT/Coimbra Chemistry Centerpt
dc.relationinfo:eu-repo/grantAgreement/FCT/POR_CENTRO/PD/BD/135287/2017/PT/Broadening the spectrum of spito-B-lactams antiviral activity: from new targets identification to the discovery of new compounds with anti-influenza activity.pt
dc.relationinfo:eu-repo/grantAgreement/FCT/OE/SFRH/BD/128910/2017/PT/Novel spiro-lactams as new antimicrobial agentspt
dc.rightsembargoedAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/pt
dc.subjectβ-lactamspt
dc.subjectδ-lactamspt
dc.subjectspiro-β-lactamspt
dc.subjectspiro-δ-lactamspt
dc.subjectpenicillanatespt
dc.subjectspirocyclizationpt
dc.titleRecent Advances in the Synthesis of Spiro‐β‐Lactams and Spiro‐δ‐Lactamspt
dc.typearticle-
degois.publication.firstPage2464pt
degois.publication.lastPage2501pt
degois.publication.issue10pt
degois.publication.titleAdvanced Synthesis & Catalysispt
dc.peerreviewedyespt
dc.identifier.doi10.1002/adsc.202100013pt
degois.publication.volume363pt
dc.date.embargo2022-01-01*
uc.date.periodoEmbargo365pt
item.grantfulltextopen-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.openairetypearticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextCom Texto completo-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.orcid0000-0001-8860-0470-
crisitem.author.orcid0000-0003-3256-4954-
Appears in Collections:I&D CQC - Artigos em Revistas Internacionais
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