摘要
A novel application of intramolecular base catalysis confers enhanced reaction rates for aminolysis ligations between peptide thioesters and peptides bearing N-terminal aspartate or glutamate residues. The broad scope of this process and its application in the total synthesis of the diabetes drug exenatide is demonstrated.
原文 | 英語 |
---|---|
頁(從 - 到) | 4770-4773 |
頁數 | 4 |
期刊 | Organic Letters |
卷 | 13 |
發行號 | 18 |
DOIs | |
出版狀態 | 已發佈 - 9月 16 2011 |
對外發佈 | 是 |
ASJC Scopus subject areas
- 生物化學
- 物理與理論化學
- 有機化學