A General Light‐Driven Organocatalytic Platform for the Activation of Inert Substrates
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
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Englisch
- Bibliographic citation
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A General Light‐Driven Organocatalytic Platform for the Activation of Inert Substrates ; day:29 ; month:06 ; year:2023 ; extent:7
Angewandte Chemie ; (29.06.2023) (gesamt 7)
- Creator
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Wu, Shuo
Schiel, Florian
Melchiorre, Paolo
- DOI
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10.1002/ange.202306364
- URN
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urn:nbn:de:101:1-2023062915423061750631
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:50 AM CEST
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Wu, Shuo
- Schiel, Florian
- Melchiorre, Paolo
Other Objects (12)
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A General Light‐Driven Organocatalytic Platform for the Activation of Inert Substrates
Light‐Driven Enantioselective Organocatalytic β‐Benzylation of Enals
Forging Fluorine‐Containing Quaternary Stereocenters by a Light‐Driven Organocatalytic Aldol Desymmetrization Process
Forging Fluorine‐Containing Quaternary Stereocenters by a Light‐Driven Organocatalytic Aldol Desymmetrization Process
Organocatalytic Carbocyclizations
Distinguishing inert Higgs doublet and inert triplet scenarios
Light-driven bioprocesses
A Dinuclear Dihydride Complex for Bimetallic Reductive Activation and Transformation of a Range of Inert Substrates
Organocatalytic C-H Hydroxylation
Organocatalytic Asymmetric Claisen Rearrangement
Organocatalytic Vinylogous Michael Additions
Hybrid nanoreactors formed by interpolyelectrolyte complex formation: a colloidal platform for light-driven catalysis †
A General Light‐Driven Organocatalytic Platform for the Activation of Inert Substrates
Light‐Driven Enantioselective Organocatalytic β‐Benzylation of Enals
Forging Fluorine‐Containing Quaternary Stereocenters by a Light‐Driven Organocatalytic Aldol Desymmetrization Process
Forging Fluorine‐Containing Quaternary Stereocenters by a Light‐Driven Organocatalytic Aldol Desymmetrization Process
Organocatalytic Carbocyclizations
Distinguishing inert Higgs doublet and inert triplet scenarios
Light-driven bioprocesses
A Dinuclear Dihydride Complex for Bimetallic Reductive Activation and Transformation of a Range of Inert Substrates
Organocatalytic C-H Hydroxylation
Organocatalytic Asymmetric Claisen Rearrangement
Organocatalytic Vinylogous Michael Additions