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.

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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
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article

Total syntheses of Kavaratamide A and 5- epi -Kavaratamide A

Fang‐Zhong Hu, Yue Chen, Tieshun Ren, Ke Lv
2 citations
Organic & Biomolecular Chemistry
Microbial Natural Products and Biosynthesis
0.90
article

Total syntheses of Kavaratamide A and 5- epi -Kavaratamide A

Fang‐Zhong Hu, Yue Chen, Tieshun Ren, Ke Lv
article en
2 citations

Abstract

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.

Organic & Biomolecular ChemistryVol. 23(7)
Nankai University (CN)
Life below water
Openalex Percentile: Top 22%
Microbial Natural Products and Biosynthesis
0.90
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