| ID | 116717 |
| 著者 |
Sato, Daiki
Tokushima University
Tsunematsu, Honoka
Tokushima University
Konishi, Isamu
Tokushima University
Komiya, Chiaki
Tokushima University
|
| 資料タイプ |
学術雑誌論文
|
| 抄録 | 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.
|
| 掲載誌名 |
Chemical Communications
|
| ISSN | 1364548X
|
| cat書誌ID | AA12455105
|
| 出版者 | The Royal Society of Chemistry
|
| 巻 | 58
|
| 号 | 17
|
| 開始ページ | 2918
|
| 終了ページ | 2921
|
| 発行日 | 2022-02-01
|
| 権利情報 | © Royal Society of Chemistry 2022
|
| EDB ID | |
| 出版社版DOI | |
| 出版社版URL | |
| フルテキストファイル | |
| 言語 |
eng
|
| 著者版フラグ |
著者版
|
| 部局 |
薬学系
生物資源系
|
