Reduction of Oximes and Hydrazones: Asymmetric and Diastereoselective Approaches

Detalhes bibliográficos
Autor(a) principal: Ribeiro, João L. P.
Data de Publicação: 2021
Outros Autores: Alves, Cláudia, Cardoso, Ana L., Lopes, Susana M. M., Pinho e Melo, Teresa M. V. D.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/107507
https://doi.org/10.2174/1385272825666210706151631
Resumo: The 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.
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spelling Reduction of Oximes and Hydrazones: Asymmetric and Diastereoselective ApproachesChiral aminesasymmetric reductionenantioselective reductiondiastereoselective reductionoximeschiral hydroxylamineshydrazoneschiral hydrazinesThe 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.Bentham Science2021info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/107507http://hdl.handle.net/10316/107507https://doi.org/10.2174/1385272825666210706151631eng13852728Ribeiro, João L. P.Alves, CláudiaCardoso, Ana L.Lopes, Susana M. M.Pinho e Melo, Teresa M. V. D.info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-18T08:02:33Zoai:estudogeral.uc.pt:10316/107507Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:23:51.130739Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Reduction of Oximes and Hydrazones: Asymmetric and Diastereoselective Approaches
title Reduction of Oximes and Hydrazones: Asymmetric and Diastereoselective Approaches
spellingShingle Reduction of Oximes and Hydrazones: Asymmetric and Diastereoselective Approaches
Ribeiro, João L. P.
Chiral amines
asymmetric reduction
enantioselective reduction
diastereoselective reduction
oximes
chiral hydroxylamines
hydrazones
chiral hydrazines
title_short Reduction of Oximes and Hydrazones: Asymmetric and Diastereoselective Approaches
title_full Reduction of Oximes and Hydrazones: Asymmetric and Diastereoselective Approaches
title_fullStr Reduction of Oximes and Hydrazones: Asymmetric and Diastereoselective Approaches
title_full_unstemmed Reduction of Oximes and Hydrazones: Asymmetric and Diastereoselective Approaches
title_sort Reduction of Oximes and Hydrazones: Asymmetric and Diastereoselective Approaches
author Ribeiro, João L. P.
author_facet Ribeiro, João L. P.
Alves, Cláudia
Cardoso, Ana L.
Lopes, Susana M. M.
Pinho e Melo, Teresa M. V. D.
author_role author
author2 Alves, Cláudia
Cardoso, Ana L.
Lopes, Susana M. M.
Pinho e Melo, Teresa M. V. D.
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Ribeiro, João L. P.
Alves, Cláudia
Cardoso, Ana L.
Lopes, Susana M. M.
Pinho e Melo, Teresa M. V. D.
dc.subject.por.fl_str_mv Chiral amines
asymmetric reduction
enantioselective reduction
diastereoselective reduction
oximes
chiral hydroxylamines
hydrazones
chiral hydrazines
topic Chiral amines
asymmetric reduction
enantioselective reduction
diastereoselective reduction
oximes
chiral hydroxylamines
hydrazones
chiral hydrazines
description The 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.
publishDate 2021
dc.date.none.fl_str_mv 2021
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/107507
http://hdl.handle.net/10316/107507
https://doi.org/10.2174/1385272825666210706151631
url http://hdl.handle.net/10316/107507
https://doi.org/10.2174/1385272825666210706151631
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 13852728
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv Bentham Science
publisher.none.fl_str_mv Bentham Science
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
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reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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