Cyaphide‐Azide 1,3‐Dipolar Cycloaddition Reactions: Scope and Applicability

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Bibliographic citation: Cyaphide‐Azide 1,3‐Dipolar Cycloaddition Reactions: Scope and Applicability ; day:10 ; month:08 ; year:2023 ; extent:9
Chemistry - a European journal ; (10.08.2023) (gesamt 9)

Creator: Yang, Eric S.
Mapp, Alex
Taylor, Andrew
Beer, Paul D.
Goicoechea, Jose M.

DOI: 10.1002/chem.202301648

URN: urn:nbn:de:101:1-2023081115040743771407

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:58 AM CEST

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Associated

Yang, Eric S.
Mapp, Alex
Taylor, Andrew
Beer, Paul D.
Goicoechea, Jose M.

Other Objects (12)

Metal Influence on Cyaphide‐Azide 1,3‐Dipolar Cycloaddition Reactions: Aromaticity and Activation Strain

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Exploration of the 1,3-dipolar cycloaddition reaction between azide and phosphorane partners and use in peptide ligation

Copper-Catalyzed Alkyne–Azide Cycloaddition by Kinetic Resolution

Is DFT Accurate Enough to Calculate Regioselectivity? The Case of 1,3‐Dipolar Cycloaddition of Azide to Alkynes and Alkenes

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

Conjugating Hemoglobin and Albumin by Strain‐Promoted Azide‐ Alkyne Cycloaddition

Alkyne–Azide Cycloaddition on Water-Soluble Copper NP–Cobaltocene Catalyst

Bioorthogonal Azide–Thioalkyne Cycloaddition Catalyzed by Photoactivatable Ruthenium(II) Complexes

Azide–Alkyne Cycloaddition with a Melanin-Supported Copper(I) Catalyst

exo-Selective Catalysts for 1,3-Dipolar Nitrone Cycloaddition

Metal Influence on Cyaphide‐Azide 1,3‐Dipolar Cycloaddition Reactions: Aromaticity and Activation Strain

Hochschulschrift

Exploration of the 1,3-dipolar cycloaddition reaction between azide and phosphorane partners and use in peptide ligation

Copper-Catalyzed Alkyne–Azide Cycloaddition by Kinetic Resolution

Is DFT Accurate Enough to Calculate Regioselectivity? The Case of 1,3‐Dipolar Cycloaddition of Azide to Alkynes and Alkenes

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

Conjugating Hemoglobin and Albumin by Strain‐Promoted Azide‐ Alkyne Cycloaddition

Alkyne–Azide Cycloaddition on Water-Soluble Copper NP–Cobaltocene Catalyst

Bioorthogonal Azide–Thioalkyne Cycloaddition Catalyzed by Photoactivatable Ruthenium(II) Complexes

Azide–Alkyne Cycloaddition with a Melanin-Supported Copper(I) Catalyst

exo-Selective Catalysts for 1,3-Dipolar Nitrone Cycloaddition

Metal Influence on Cyaphide‐Azide 1,3‐Dipolar Cycloaddition Reactions: Aromaticity and Activation Strain

Hochschulschrift

Exploration of the 1,3-dipolar cycloaddition reaction between azide and phosphorane partners and use in peptide ligation

Copper-Catalyzed Alkyne–Azide Cycloaddition by Kinetic Resolution

Is DFT Accurate Enough to Calculate Regioselectivity? The Case of 1,3‐Dipolar Cycloaddition of Azide to Alkynes and Alkenes

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

Conjugating Hemoglobin and Albumin by Strain‐Promoted Azide‐ Alkyne Cycloaddition

Alkyne–Azide Cycloaddition on Water-Soluble Copper NP–Cobaltocene Catalyst

Bioorthogonal Azide–Thioalkyne Cycloaddition Catalyzed by Photoactivatable Ruthenium(II) Complexes

Azide–Alkyne Cycloaddition with a Melanin-Supported Copper(I) Catalyst

exo-Selective Catalysts for 1,3-Dipolar Nitrone Cycloaddition

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Cyaphide‐Azide 1,3‐Dipolar Cycloaddition Reactions: Scope and Applicability

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Other Objects (12)

Metal Influence on Cyaphide‐Azide 1,3‐Dipolar Cycloaddition Reactions: Aromaticity and Activation Strain

Exploration of the 1,3-dipolar cycloaddition reaction between azide and phosphorane partners and use in peptide ligation

Copper-Catalyzed Alkyne–Azide Cycloaddition by Kinetic Resolution

Is DFT Accurate Enough to Calculate Regioselectivity? The Case of 1,3‐Dipolar Cycloaddition of Azide to Alkynes and Alkenes

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

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

Conjugating Hemoglobin and Albumin by Strain‐Promoted Azide‐ Alkyne Cycloaddition

Alkyne–Azide Cycloaddition on Water-Soluble Copper NP–Cobaltocene Catalyst

Bioorthogonal Azide–Thioalkyne Cycloaddition Catalyzed by Photoactivatable Ruthenium(II) Complexes

Bioorthogonal Azide–Thioalkyne Cycloaddition Catalyzed by Photoactivatable Ruthenium(II) Complexes

Azide–Alkyne Cycloaddition with a Melanin-Supported Copper(I) Catalyst

exo-Selective Catalysts for 1,3-Dipolar Nitrone Cycloaddition

Metal Influence on Cyaphide‐Azide 1,3‐Dipolar Cycloaddition Reactions: Aromaticity and Activation Strain

Exploration of the 1,3-dipolar cycloaddition reaction between azide and phosphorane partners and use in peptide ligation

Copper-Catalyzed Alkyne–Azide Cycloaddition by Kinetic Resolution

Is DFT Accurate Enough to Calculate Regioselectivity? The Case of 1,3‐Dipolar Cycloaddition of Azide to Alkynes and Alkenes

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

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

Conjugating Hemoglobin and Albumin by Strain‐Promoted Azide‐ Alkyne Cycloaddition

Alkyne–Azide Cycloaddition on Water-Soluble Copper NP–Cobaltocene Catalyst

Bioorthogonal Azide–Thioalkyne Cycloaddition Catalyzed by Photoactivatable Ruthenium(II) Complexes

Bioorthogonal Azide–Thioalkyne Cycloaddition Catalyzed by Photoactivatable Ruthenium(II) Complexes

Azide–Alkyne Cycloaddition with a Melanin-Supported Copper(I) Catalyst

exo-Selective Catalysts for 1,3-Dipolar Nitrone Cycloaddition

Metal Influence on Cyaphide‐Azide 1,3‐Dipolar Cycloaddition Reactions: Aromaticity and Activation Strain

Exploration of the 1,3-dipolar cycloaddition reaction between azide and phosphorane partners and use in peptide ligation

Copper-Catalyzed Alkyne–Azide Cycloaddition by Kinetic Resolution

Is DFT Accurate Enough to Calculate Regioselectivity? The Case of 1,3‐Dipolar Cycloaddition of Azide to Alkynes and Alkenes

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

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

Conjugating Hemoglobin and Albumin by Strain‐Promoted Azide‐ Alkyne Cycloaddition

Alkyne–Azide Cycloaddition on Water-Soluble Copper NP–Cobaltocene Catalyst

Bioorthogonal Azide–Thioalkyne Cycloaddition Catalyzed by Photoactivatable Ruthenium(II) Complexes

Bioorthogonal Azide–Thioalkyne Cycloaddition Catalyzed by Photoactivatable Ruthenium(II) Complexes

Azide–Alkyne Cycloaddition with a Melanin-Supported Copper(I) Catalyst

exo-Selective Catalysts for 1,3-Dipolar Nitrone Cycloaddition

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