| ID | 116717 |
| Author |
Sato, Daiki
Tokushima University
Denda, Masaya
Tokushima University
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Tsunematsu, Honoka
Tokushima University
Tanaka, Naonobu
Tokushima University
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Konishi, Isamu
Tokushima University
Komiya, Chiaki
Tokushima University
Otaka, Akira
Tokushima University
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|
| Content Type |
Journal Article
|
| Description | Intramolecular S-acylation of a thiol-installed threonine with a thioester unit, followed by S–O acyl transfer and subsequent desulphurisation, allows the synthesis of lactone peptides. A protocol has been developed enabling the cyclisation of a linear peptide, a reaction which has not been achieved by conventional methods.
|
| Journal Title |
Chemical Communications
|
| ISSN | 1364548X
|
| NCID | AA12455105
|
| Publisher | The Royal Society of Chemistry
|
| Volume | 58
|
| Issue | 17
|
| Start Page | 2918
|
| End Page | 2921
|
| Published Date | 2022-02-01
|
| Rights | © Royal Society of Chemistry 2022
|
| EDB ID | |
| DOI (Published Version) | |
| URL ( Publisher's Version ) | |
| FullText File | |
| language |
eng
|
| TextVersion |
Author
|
| departments |
Pharmaceutical Sciences
Bioscience and Bioindustry
|
