Article ; Online: N-Terminal Proline Editing for the Synthesis of Peptides with Mercaptoproline and Selenoproline: Mechanistic Insights Lead to Greater Efficiency in Proline Native Chemical Ligation.
ACS chemical biology
2024 Volume 19, Issue 2, Page(s) 536–550
Abstract: Native chemical ligation (NCL) at proline has been limited by cost and synthetic access. In addition, prior examples of NCL using mercaptoproline have exhibited stalling of the reaction after thioester exchange, due to ... ...
Abstract | Native chemical ligation (NCL) at proline has been limited by cost and synthetic access. In addition, prior examples of NCL using mercaptoproline have exhibited stalling of the reaction after thioester exchange, due to inefficient |
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MeSH term(s) | Proline ; Hydroxyproline ; Peptides/chemistry ; Amides ; Sulfur Compounds |
Chemical Substances | Proline (9DLQ4CIU6V) ; Hydroxyproline (RMB44WO89X) ; Peptides ; Amides ; Sulfur Compounds |
Language | English |
Publishing date | 2024-02-07 |
Publishing country | United States |
Document type | Journal Article |
ISSN | 1554-8937 |
ISSN (online) | 1554-8937 |
DOI | 10.1021/acschembio.3c00705 |
Database | MEDical Literature Analysis and Retrieval System OnLINE |
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