Controlling alkyne reactivity by means of a copper-catalyzed radical reaction system for the synthesis of functionalized quaternary carbons

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Bibliographic citation: Controlling alkyne reactivity by means of a copper-catalyzed radical reaction system for the synthesis of functionalized quaternary carbons ; volume:16 ; pages:502-508
Beilstein journal of organic chemistry ; 16, 502-508

Classification: Chemie

DOI: 10.3762/bjoc.16.45

URN: urn:nbn:de:101:1-2021012207583932889040

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:35 AM CEST

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Controlling alkyne reactivity by means of a copper-catalyzed radical reaction system for the synthesis of functionalized quaternary carbons

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Other Objects (12)

Copper-Catalyzed Alkyne–Azide Cycloaddition by Kinetic Resolution

Conditional Copper‐Catalyzed Azide–Alkyne Cycloaddition by Catalyst Encapsulation †

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Advancements in the mechanistic understanding of the copper-catalyzed azide–alkyne cycloaddition

Alkyne-Functionalized Cyclooctyne on Si(001): Reactivity Studies and Surface Bonding from an Energy Decomposition Analysis Perspective

Copper‐Catalyzed C (sp 3)−H α‐Acetylation: Generation of Quaternary Centers

Copper‐Catalyzed C (sp 3)−H α‐Acetylation: Generation of Quaternary Centers

Computational Study of Alkyne‐Acid Cycloisomerization in Gold‐Functionalized Resorcinarene Cavitand

Double Nitroxide Labeling by Copper-Catalyzed Azide–Alkyne Cycloadditions with Noncanonical Amino Acids for Electron Paramagnetic Resonance Spectroscopy

Cationic Tungsten Alkylidyne N ‐Heterocyclic Carbene Complexes: Synthesis and Reactivity in Alkyne Metathesis

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Conditional Copper‐Catalyzed Azide–Alkyne Cycloaddition by Catalyst Encapsulation †

Conditional Copper‐Catalyzed Azide–Alkyne Cycloaddition by Catalyst Encapsulation †

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Copper‐Catalyzed C (sp 3)−H α‐Acetylation: Generation of Quaternary Centers

Copper‐Catalyzed C (sp 3)−H α‐Acetylation: Generation of Quaternary Centers

Computational Study of Alkyne‐Acid Cycloisomerization in Gold‐Functionalized Resorcinarene Cavitand

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Cationic Tungsten Alkylidyne N ‐Heterocyclic Carbene Complexes: Synthesis and Reactivity in Alkyne Metathesis

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Conditional Copper‐Catalyzed Azide–Alkyne Cycloaddition by Catalyst Encapsulation †

Conditional Copper‐Catalyzed Azide–Alkyne Cycloaddition by Catalyst Encapsulation †

Advancements in the mechanistic understanding of the copper-catalyzed azide–alkyne cycloaddition

Alkyne-Functionalized Cyclooctyne on Si(001): Reactivity Studies and Surface Bonding from an Energy Decomposition Analysis Perspective

Copper‐Catalyzed C (sp 3)−H α‐Acetylation: Generation of Quaternary Centers

Copper‐Catalyzed C (sp 3)−H α‐Acetylation: Generation of Quaternary Centers

Computational Study of Alkyne‐Acid Cycloisomerization in Gold‐Functionalized Resorcinarene Cavitand

Double Nitroxide Labeling by Copper-Catalyzed Azide–Alkyne Cycloadditions with Noncanonical Amino Acids for Electron Paramagnetic Resonance Spectroscopy

Cationic Tungsten Alkylidyne N ‐Heterocyclic Carbene Complexes: Synthesis and Reactivity in Alkyne Metathesis

Reactivity of a Dihydrodiborene with CO: Coordination, Insertion, Cleavage and Spontaneous Cyclic Alkyne Formation

Synthesis, Isolation and Reactivity of Silyl-Substituted Functionalized Silylenes

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