Journal
ORGANIC LETTERS
Volume 11, Issue 12, Pages 2655-2658Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol9006794
Keywords
-
Categories
Funding
- Japan Society for Promotion of Science [16380142]
- Ministry of Education, Culture, Sports, Science, and Technology [16073207]
- Drugs for Neglected Diseases initiative
- All Kitasato Project Study
- Grants-in-Aid for Scientific Research [16073207, 16380142] Funding Source: KAKEN
Ask authors/readers for more resources
Merobatzelladines A (1) and B (2) have been isolated from a marine sponge Monanchora sp. as antibacterial constituents. Their structures including relative stereochemistry were determined by interpretation of spectral data. The absolute stereochemistry of merobatzelladine B (2) was elucidated after introduction of the fourth ring system preinstalled with a secondary hydroxyl group to which the modified Mosher method was applied. Merobatzelladines exhibit moderate anti-infective activity against a bacterium and protozoa.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available