N‐Terminal‐Specific Dual Modification of Peptides through Copper‐Catalyzed [3+2] Cycloaddition
Article Properties
-
LanguageEnglish
-
DOI (url)
-
Publication Date2024/02/12
-
Journal
-
Indian UGC (journal)
-
Refrences92
-
Haruka Machida Faculty of Science and Engineering Chuo University 1-13-27 Kasuga Bunkyo-ku Tokyo 112-8551 Japan
-
Kazuya Kanemoto Faculty of Science and Engineering Chuo University 1-13-27 Kasuga Bunkyo-ku Tokyo 112-8551 JapanGraduate School of Pharmaceutical Sciences Tohoku University 6-3 Aoba, Aramaki, Aoba-ku Sendai 980-8578 Japan ORCID (unauthenticated)
Abstract
Cite
Machida, Haruka, and Kazuya Kanemoto. “N‐Terminal‐Specific Dual Modification of Peptides through Copper‐Catalyzed [3+2] Cycloaddition”. Angewandte Chemie, vol. 136, no. 12, 2024, https://doi.org/10.1002/ange.202320012.
Machida, H., & Kanemoto, K. (2024). N‐Terminal‐Specific Dual Modification of Peptides through Copper‐Catalyzed [3+2] Cycloaddition. Angewandte Chemie, 136(12). https://doi.org/10.1002/ange.202320012
Machida, Haruka, and Kazuya Kanemoto. “N‐Terminal‐Specific Dual Modification of Peptides through Copper‐Catalyzed [3+2] Cycloaddition”. Angewandte Chemie 136, no. 12 (2024). https://doi.org/10.1002/ange.202320012.
Machida H, Kanemoto K. N‐Terminal‐Specific Dual Modification of Peptides through Copper‐Catalyzed [3+2] Cycloaddition. Angewandte Chemie. 2024;136(12).
Refrences
| Title | Journal | Journal Categories | Citations | Publication Date |
|---|---|---|---|---|
| 10.1039/D0SC01153C | ||||
| Drug Carriers for the Delivery of Therapeutic Peptides | Biomacromolecules |
| 147 | 2014 |
| Click Chemistry in Peptide-Based Drug Design | Molecules |
| 137 | 2013 |
Chemical Conjugation to Less Targeted Proteinogenic Amino Acids | ChemBioChem |
| 21 | 2022 |
Selective N-terminal acylation of peptides and proteins with a Gly-His tag sequence | Nature Communications |
| 42 | 2018 |