Issue 9, 2018

Total synthesis of teixobactin and its stereoisomers

Abstract

Teixobactin is a depsipeptide natural product with potent antibiotic activity against a range of Gram-positive multi-drug resistant bacteria. Its composition features a unique L-allo-enduracididine (allo-End10), three Iles2/6/11 residues, and one D-allo-Ile5 residue. Intrigued by the potential biological impact of the stereochemistry of these residues, we synthesized teixobactin and three of its stereoisomers carrying L-End10, D-End10 or D-allo-End10. In addition, stereoisomers with D-allo-Ile shuffled to positions 2, 6 or 11 were prepared. Our synthetic strategy uses the combined methods of solution and solid phase peptide synthesis. The solution phase synthesis overcomes the racemization issue for ester coupling between Ile11 and Thr8. The solid phase synthesis improves efficiency and convergence. This method also allows the efficient preparation of fluorescent-labeled analogs of teixobactin.

Graphical abstract: Total synthesis of teixobactin and its stereoisomers

Supplementary files

Article information

Article type
Research Article
Submitted
06 ፌብሩ 2018
Accepted
23 ፌብሩ 2018
First published
24 ፌብሩ 2018

Org. Chem. Front., 2018,5, 1431-1435

Total synthesis of teixobactin and its stereoisomers

L. Liu, S. Wu, Q. Wang, M. Zhang, B. Wang, G. He and G. Chen, Org. Chem. Front., 2018, 5, 1431 DOI: 10.1039/C8QO00145F

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements