Organometallic reagents primed for peptide modification
| dc.contributor.author | Elgindy, Cecile | en |
| dc.contributor.author | Malins, Lara R. | en |
| dc.date.accessioned | 2025-12-31T19:41:11Z | |
| dc.date.available | 2025-12-31T19:41:11Z | |
| dc.date.issued | 2021-09-16 | en |
| dc.description.abstract | In this issue of Chem Catalysis, Walczak and co-workers introduce a carbastannatrane alanine derivative that facilitates amino acid side-chain functionalizations via C–C, C–S, and C–Se bond formation using Stille cross-coupling reactions. Applications in late-stage peptide modifications and macrocyclizations further exemplify the value of this novel building block. | en |
| dc.description.status | Peer-reviewed | en |
| dc.format.extent | 3 | en |
| dc.identifier.issn | 2667-1107 | en |
| dc.identifier.scopus | 85126079376 | en |
| dc.identifier.uri | https://hdl.handle.net/1885/733798020 | |
| dc.language.iso | en | en |
| dc.rights | Publisher Copyright: © 2021 Elsevier Inc. | en |
| dc.source | Chem Catalysis | en |
| dc.title | Organometallic reagents primed for peptide modification | en |
| dc.type | Commentary | en |
| dspace.entity.type | Publication | en |
| local.bibliographicCitation.lastpage | 760 | en |
| local.bibliographicCitation.startpage | 758 | en |
| local.contributor.affiliation | Elgindy, Cecile; Research School of Chemistry, ANU College of Science and Medicine, The Australian National University | en |
| local.contributor.affiliation | Malins, Lara R.; Research School of Chemistry, ANU College of Science and Medicine, The Australian National University | en |
| local.identifier.citationvolume | 1 | en |
| local.identifier.doi | 10.1016/j.checat.2021.06.020 | en |
| local.identifier.pure | a897db34-05ce-4a62-b7e6-0eccef734c10 | en |
| local.identifier.url | https://www.scopus.com/pages/publications/85126079376 | en |
| local.type.status | Published | en |