Decoration of Coiled-Coil Peptides with N-Cysteine Peptide Thioesters As Cyclic Peptide Precursors Using Copper-Catalyzed Azide–Alkyne Cycloaddition (CuAAC) Click Reaction-Reference-Cited by-同舟云学术

Decoration of Coiled-Coil Peptides with N-Cysteine Peptide Thioesters As Cyclic Peptide Precursors Using Copper-Catalyzed Azide–Alkyne Cycloaddition (CuAAC) Click Reaction

Published:2018-11-08 Issue:23 Volume:20 Page:7493-7497
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Rink W. Mathis¹,Thomas Franziska¹²^ORCID

Affiliation:

1. Institute of Organic and Biomolecular Chemistry, Georg-August Universität Göttingen, Tammannstraße 2, 37077 Göttingen, Germany

2. Center for Biostructural Imaging of Neurodegeneration, von-Siebold-Straße 3a, 37075 Göttingen, Germany

Funder

Deutsche Forschungsgemeinschaft

Verband der Chemischen Industrie

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.8b03261

Reference45 articles.

1. Peptidotriazoles on Solid Phase: [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides

2. A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective “Ligation” of Azides and Terminal Alkynes

3. Peptide Conjugation via CuAAC ‘Click’ Chemistry

4. Bioorthogonal Chemistry: Fishing for Selectivity in a Sea of Functionality

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