Highly Efficient Cyclization Approach of Propargylated Peptides via Gold(I)-Mediated Sequential C–N, C–O, and C–C Bond Formation
Author:
Affiliation:
1. Schulich Faculty of Chemistry, Technion-Israel Institute of Technology, Haifa 3200008, Israel
Funder
H2020 European Research Council
Publisher
American Chemical Society (ACS)
Subject
General Chemical Engineering,General Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acscentsci.1c00969
Reference38 articles.
1. How proteins bind macrocycles
2. Getting in Shape: Controlling Peptide Bioactivity and Bioavailability Using Conformational Constraints
3. Contemporary strategies for peptide macrocyclization
4. Ligation Technologies for the Synthesis of Cyclic Peptides
5. Synthesis of All-l Cyclic Tetrapeptides Using Pseudoprolines as Removable Turn Inducers
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