Molybdenum Catalyzed Acceptorless Dehydrogenation of Alcohols for the Synthesis of Quinolines
Autor(a) principal: | |
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Data de Publicação: | 2024 |
Outros Autores: | |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
Texto Completo: | http://hdl.handle.net/10362/182881 |
Resumo: | Funding Information: . The authors thank Fundação para a Ciência e a Tecnologia (FCT) for projects 10.54499/PTDC/QUI‐QIN/0359/2021, MOSTMICRO‐ITQB, UIDB/04612/20220 and UIPD/04612/2020. The National NMR Facility is supported by CERMAX through project 022162. We also thank C. Almeida for elemental analysis and mass spectrometry at ITQB laboratories. ESI‐HRMS data were provided by the Mass Spectrometry Unit (UniMS), ITQB/IBET. The authors would like to thank the Crystallography Service of the LAQV, Department of Chemistry, NOVA School of Science and Technology, Portugal, for the structural determination of the complexes and 1 6 Publisher Copyright: © 2024 The Authors. ChemCatChem published by Wiley-VCH GmbH. |
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Molybdenum Catalyzed Acceptorless Dehydrogenation of Alcohols for the Synthesis of Quinolinesacceptorless dehydrogenative couplingMolybdenumquinolinestriazolylideneCatalysisPhysical and Theoretical ChemistryOrganic ChemistryInorganic ChemistryFunding Information: . The authors thank Fundação para a Ciência e a Tecnologia (FCT) for projects 10.54499/PTDC/QUI‐QIN/0359/2021, MOSTMICRO‐ITQB, UIDB/04612/20220 and UIPD/04612/2020. The National NMR Facility is supported by CERMAX through project 022162. We also thank C. Almeida for elemental analysis and mass spectrometry at ITQB laboratories. ESI‐HRMS data were provided by the Mass Spectrometry Unit (UniMS), ITQB/IBET. The authors would like to thank the Crystallography Service of the LAQV, Department of Chemistry, NOVA School of Science and Technology, Portugal, for the structural determination of the complexes and 1 6 Publisher Copyright: © 2024 The Authors. ChemCatChem published by Wiley-VCH GmbH.The first molybdenum triazolylidene complexes catalyzing the atom-economical synthesis of quinolines through acceptorless dehydrogenative coupling of alcohols is reported. A new family of Mo(0) complexes bearing chelating bis-1,2,3-triazolylidene, pyridyl-1,2,3-triazolylidene, and bis-triazole ligands have been prepared and applied as catalysts for the synthesis of quinolines. Interestingly, Mo complexes bearing bis-1,2,3-triazolylidene ligands with alkyl groups (Et, n-Bu) displayed superior catalytic activities than those containing aryl substituents on the triazolylidene rings. Control experiments corroborated that the catalytic reaction involves the dehydrogenation pathway.Instituto de Tecnologia Química e Biológica António Xavier (ITQB)RUNGarcia, BeatrizRoyo, Beatriz2025-05-08T21:30:40Z2024-02-232024-02-23T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10362/182881eng1867-3880PURE: 90641809https://doi.org/10.1002/cctc.202400024info:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2025-05-19T01:40:15Zoai:run.unl.pt:10362/182881Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-29T07:14:13.445424Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse |
dc.title.none.fl_str_mv |
Molybdenum Catalyzed Acceptorless Dehydrogenation of Alcohols for the Synthesis of Quinolines |
title |
Molybdenum Catalyzed Acceptorless Dehydrogenation of Alcohols for the Synthesis of Quinolines |
spellingShingle |
Molybdenum Catalyzed Acceptorless Dehydrogenation of Alcohols for the Synthesis of Quinolines Garcia, Beatriz acceptorless dehydrogenative coupling Molybdenum quinolines triazolylidene Catalysis Physical and Theoretical Chemistry Organic Chemistry Inorganic Chemistry |
title_short |
Molybdenum Catalyzed Acceptorless Dehydrogenation of Alcohols for the Synthesis of Quinolines |
title_full |
Molybdenum Catalyzed Acceptorless Dehydrogenation of Alcohols for the Synthesis of Quinolines |
title_fullStr |
Molybdenum Catalyzed Acceptorless Dehydrogenation of Alcohols for the Synthesis of Quinolines |
title_full_unstemmed |
Molybdenum Catalyzed Acceptorless Dehydrogenation of Alcohols for the Synthesis of Quinolines |
title_sort |
Molybdenum Catalyzed Acceptorless Dehydrogenation of Alcohols for the Synthesis of Quinolines |
author |
Garcia, Beatriz |
author_facet |
Garcia, Beatriz Royo, Beatriz |
author_role |
author |
author2 |
Royo, Beatriz |
author2_role |
author |
dc.contributor.none.fl_str_mv |
Instituto de Tecnologia Química e Biológica António Xavier (ITQB) RUN |
dc.contributor.author.fl_str_mv |
Garcia, Beatriz Royo, Beatriz |
dc.subject.por.fl_str_mv |
acceptorless dehydrogenative coupling Molybdenum quinolines triazolylidene Catalysis Physical and Theoretical Chemistry Organic Chemistry Inorganic Chemistry |
topic |
acceptorless dehydrogenative coupling Molybdenum quinolines triazolylidene Catalysis Physical and Theoretical Chemistry Organic Chemistry Inorganic Chemistry |
description |
Funding Information: . The authors thank Fundação para a Ciência e a Tecnologia (FCT) for projects 10.54499/PTDC/QUI‐QIN/0359/2021, MOSTMICRO‐ITQB, UIDB/04612/20220 and UIPD/04612/2020. The National NMR Facility is supported by CERMAX through project 022162. We also thank C. Almeida for elemental analysis and mass spectrometry at ITQB laboratories. ESI‐HRMS data were provided by the Mass Spectrometry Unit (UniMS), ITQB/IBET. The authors would like to thank the Crystallography Service of the LAQV, Department of Chemistry, NOVA School of Science and Technology, Portugal, for the structural determination of the complexes and 1 6 Publisher Copyright: © 2024 The Authors. ChemCatChem published by Wiley-VCH GmbH. |
publishDate |
2024 |
dc.date.none.fl_str_mv |
2024-02-23 2024-02-23T00:00:00Z 2025-05-08T21:30:40Z |
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 |
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http://hdl.handle.net/10362/182881 |
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http://hdl.handle.net/10362/182881 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
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1867-3880 PURE: 90641809 https://doi.org/10.1002/cctc.202400024 |
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info:eu-repo/semantics/openAccess |
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openAccess |
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Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia |
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