Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/107507
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dc.contributor.authorRibeiro, João L. P.-
dc.contributor.authorAlves, Cláudia-
dc.contributor.authorCardoso, Ana L.-
dc.contributor.authorLopes, Susana M. M.-
dc.contributor.authorPinho e Melo, Teresa M. V. D.-
dc.date.accessioned2023-07-17T12:02:59Z-
dc.date.available2023-07-17T12:02:59Z-
dc.date.issued2021-
dc.identifier.issn13852728pt
dc.identifier.urihttps://hdl.handle.net/10316/107507-
dc.description.abstractThe asymmetric reduction of oximes and hydrazones is an attractive and versatile strategy for the synthesis of chiral amines, which are valuable building blocks in organic synthesis. This review summarizes the relevant developments, made in the last decade, on the enantioselective and diastereoselective reduction of oximes and hydrazones involving metal-catalyzed hydrogenation/hydrogenolysis reactions, hydride donor reactions, and electrochemical reactions.pt
dc.language.isoengpt
dc.publisherBentham Sciencept
dc.relationUIDB/00313/2020pt
dc.relationUIDP/QUI/00313/2020pt
dc.relationPD/BD/143160/2019pt
dc.relationPD/BD/143159/2019pt
dc.rightsembargoedAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subjectChiral aminespt
dc.subjectasymmetric reductionpt
dc.subjectenantioselective reductionpt
dc.subjectdiastereoselective reductionpt
dc.subjectoximespt
dc.subjectchiral hydroxylaminespt
dc.subjecthydrazonespt
dc.subjectchiral hydrazinespt
dc.titleReduction of Oximes and Hydrazones: Asymmetric and Diastereoselective Approachespt
dc.typearticle-
degois.publication.firstPage2175pt
degois.publication.lastPage2198pt
degois.publication.issue19pt
degois.publication.titleCurrent Organic Chemistrypt
dc.peerreviewedyespt
dc.identifier.doi10.2174/1385272825666210706151631pt
degois.publication.volume25pt
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.orcid0000-0002-5185-3930-
crisitem.author.orcid0000-0003-0551-7255-
crisitem.author.orcid0000-0002-1580-5667-
crisitem.author.orcid0000-0003-3256-4954-
Appears in Collections:I&D CQC - Artigos em Revistas Internacionais
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This item is licensed under a Creative Commons License Creative Commons