Total syntheses of Kavaratamide A and 5- <i>epi</i> -Kavaratamide A
The total synthesis of Kavaratamide A, a new Linear Lipodepsipeptide from the Marine Cyanobacterium <i>Moorena bouillonii</i> was achieved by assembling the side chain in stage through condensation coupling, carbon-chain extension, Steglich esterification and Evans aldol reaction. In addition, total synthesis of Kavaratamide A's isomer, 5-<i>epi</i>-kavaratamide A, is also successfully achieved. Cytotoxicity test suggested that Kavaratamide A and 5-<i>epi</i>-Kavaratamide A have a moderate bioactivity against cancer cells.
Authors
- Fang‐Zhong Hu (ORCID: https://orcid.org/0000-0002-5422-9455)
- Yue Chen (ORCID: https://orcid.org/0000-0001-8888-1452)
- Tieshun Ren
- Ke Lv
Institutions
- Nankai University (CN)
Publication Details
- Journal
- Organic & Biomolecular Chemistry
- Published
- 2024-11-26
- DOI
- https://doi.org/10.1039/d4ob01409j
- Citations
- 2
- Primary Topic
- Microbial Natural Products and Biosynthesis
- Type
- article
- Field-Weighted Citation Impact
- 0.90