Pd-Catalyzed Allylic Substitution using Nucleophilic Amines: Access to Functionalized Mono- and Bis-N-Allyl Synthons

dc.contributor.author
Gao, Fengyun
dc.contributor.author
Ghorai, Debasish
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Benet-Buchholz, Jordi
dc.contributor.author
Kleij, Arjan W.
dc.date.accessioned
2024-09-09T13:54:58Z
dc.date.accessioned
2024-12-16T11:52:19Z
dc.date.available
2025-08-09T22:45:09Z
dc.date.issued
2024-08-09
dc.identifier.uri
http://hdl.handle.net/2072/537803
dc.description.abstract
We here report a catalytic strategy to enable the decarboxylative allylic amination of vinyl cyclic carbonates using various aliphatic and nucleophilic amines. The use of a protic medium and chelating diphosphine ligands is a main driver towards chemo-selective allylic amine formation, thereby minimizing undesired ligand-driven complex speciation and aminolysis of the involved substrate. This improved approach amplifies the repertoire of allylic amine synthons that can be prepared from a variety of substrate combinations.
eng
dc.format.extent
9 p.
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dc.language.iso
eng
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dc.publisher
Wiley-VCH
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dc.rights
CC-BY 4.0
dc.source
RECERCAT (Dipòsit de la Recerca de Catalunya)
dc.subject.other
Química
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dc.title
Pd-Catalyzed Allylic Substitution using Nucleophilic Amines: Access to Functionalized Mono- and Bis-N-Allyl Synthons
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dc.type
info:eu-repo/semantics/article
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dc.type
info:eu-repo/semantics/acceptedVersion
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dc.subject.udc
54 - Química
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dc.relation.projectID
CERCA Program/Generalitat de Catalunya
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dc.relation.projectID
ICREA
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dc.relation.projectID
Ministerio de Ciencia e Innovación (PID2020-112684GB-100, and Severo Ochoa Excellence Accreditation 2020–2023 CEX2019-000925-S)
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dc.relation.projectID
AGAUR (2021-SGR-00853)
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dc.relation.projectID
.FG thanks the Chinese Research Council (CSC) for a predoctoral fellowship (2021-06180010)
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dc.relation.projectID
DG appreciates postdoctoral funding from AGAUR (2018-BP-00243) and AEI (PCI2021-122021-2B)
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dc.identifier.doi
https://doi.org/10.1002/adsc.202400685
dc.rights.accessLevel
info:eu-repo/semantics/openAccess


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