This thesis focuses on the development of efficient and scalable total syntheses of natural products that can be used as preferred scaffolds for anti-infective drug discovery. It describes the total synthesis of two classes of antimicrobial non-ribosomal peptides (NRPs) - teixobactin and the skyllamycins - with subsequent biological evaluation. The first part describes the first total synthesis of teixobactin by means of a solid-phase peptide synthesis-macrolactamisation approach, yielding a synthetic natural product that can combat a number of clinically relevant Gram-positive bacterial pathogens. The second part describes the first total synthesis of skyllamycins A-C, a family of structurally complex cyclic NRPs, which inhibit the growth of the Pseudomonas aeruginosa biofilms that are responsible for significant mortality among cystic fibrosis patients.
ISBN: | 9789811088056 |
Publication date: | 14th May 2018 |
Author: | Andrew Giltrap |
Publisher: | Springer an imprint of Springer Nature Singapore |
Format: | Hardback |
Pagination: | 268 pages |
Series: | Springer Theses |
Genres: |
Medicinal chemistry Medical microbiology and virology |