Double Nitroxide Labeling by Copper-Catalyzed Azide–Alkyne Cycloadditions with Noncanonical Amino Acids for Electron Paramagnetic Resonance Spectroscopy
- 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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In: ACS Chemical Biology ; 14 (2019), 5. - S. 839-844. - ISSN 1554-8929. - eISSN 1554-8937
- Classification
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Chemie
- Event
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Veröffentlichung
- (where)
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Konstanz
- (who)
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KOPS Universität Konstanz
- (when)
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2019
- Creator
- URN
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urn:nbn:de:bsz:352-2-zfywk5o2w02p4
- Rights
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:47 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Widder, Pia
- Berner, Frederic
- Summerer, Daniel
- Drescher, Malte
- KOPS Universität Konstanz
Time of origin
- 2019
Other Objects (12)
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Conditional Copper‐Catalyzed Azide–Alkyne Cycloaddition by Catalyst Encapsulation †
Highly active dinuclear copper catalysts for homogeneous azide-alkyne cycloadditions
Highly Active Dinuclear Copper Catalysts for Homogeneous Azide-Alkyne Cycloadditions
Chemoselectivity of Tertiary Azides in Strain‐Promoted Alkyne‐Azide Cycloadditions
Advancements in the mechanistic understanding of the copper-catalyzed azide–alkyne cycloaddition
Live Monitoring of Strain‐Promoted Azide Alkyne Cycloadditions in Complex Reaction Environments by Inline ATR‐IR Spectroscopy
Development of Copper-Catalyzed Cycloadditions and Organocatalyzed Domino Reactions
A 66‐Nuclear All‐Alkynyl Protected Peanut‐Shaped Silver (I)/Copper (I) Heterometallic Nanocluster: Intermediate in Copper‐Catalyzed Alkyne‐Azide Cycloaddition
Alkyne–Azide Cycloaddition on Water-Soluble Copper NP–Cobaltocene Catalyst
Conjugating Hemoglobin and Albumin by Strain‐Promoted Azide‐ Alkyne Cycloaddition
Copper-Catalyzed Alkyne–Azide Cycloaddition by Kinetic Resolution
Conditional Copper‐Catalyzed Azide–Alkyne Cycloaddition by Catalyst Encapsulation †
Conditional Copper‐Catalyzed Azide–Alkyne Cycloaddition by Catalyst Encapsulation †
Highly active dinuclear copper catalysts for homogeneous azide-alkyne cycloadditions
Highly Active Dinuclear Copper Catalysts for Homogeneous Azide-Alkyne Cycloadditions
Chemoselectivity of Tertiary Azides in Strain‐Promoted Alkyne‐Azide Cycloadditions
Advancements in the mechanistic understanding of the copper-catalyzed azide–alkyne cycloaddition
Live Monitoring of Strain‐Promoted Azide Alkyne Cycloadditions in Complex Reaction Environments by Inline ATR‐IR Spectroscopy
Development of Copper-Catalyzed Cycloadditions and Organocatalyzed Domino Reactions
A 66‐Nuclear All‐Alkynyl Protected Peanut‐Shaped Silver (I)/Copper (I) Heterometallic Nanocluster: Intermediate in Copper‐Catalyzed Alkyne‐Azide Cycloaddition
Alkyne–Azide Cycloaddition on Water-Soluble Copper NP–Cobaltocene Catalyst
Conjugating Hemoglobin and Albumin by Strain‐Promoted Azide‐ Alkyne Cycloaddition
Copper-Catalyzed Alkyne–Azide Cycloaddition by Kinetic Resolution
Conditional Copper‐Catalyzed Azide–Alkyne Cycloaddition by Catalyst Encapsulation †
Conditional Copper‐Catalyzed Azide–Alkyne Cycloaddition by Catalyst Encapsulation †
Highly active dinuclear copper catalysts for homogeneous azide-alkyne cycloadditions
Highly Active Dinuclear Copper Catalysts for Homogeneous Azide-Alkyne Cycloadditions
Chemoselectivity of Tertiary Azides in Strain‐Promoted Alkyne‐Azide Cycloadditions
Advancements in the mechanistic understanding of the copper-catalyzed azide–alkyne cycloaddition
Live Monitoring of Strain‐Promoted Azide Alkyne Cycloadditions in Complex Reaction Environments by Inline ATR‐IR Spectroscopy
Development of Copper-Catalyzed Cycloadditions and Organocatalyzed Domino Reactions
A 66‐Nuclear All‐Alkynyl Protected Peanut‐Shaped Silver (I)/Copper (I) Heterometallic Nanocluster: Intermediate in Copper‐Catalyzed Alkyne‐Azide Cycloaddition
Alkyne–Azide Cycloaddition on Water-Soluble Copper NP–Cobaltocene Catalyst