Total synthesis of jamaicamide B.
Org Biomol Chem
; 22(23): 4637-4640, 2024 06 12.
Article
in En
| MEDLINE
| ID: mdl-38716558
ABSTRACT
Jamaicamide B was isolated from the cyanobacterium Moorea producens in Jamaica and shows neurotoxicity. This unique mixed peptide-polyketide structure contains a pyrrolinone ring, a ß-methoxy enone, an (E)-olefin, an undetermined stereocenter at C9, an (E)-chloroolefin, and a terminal alkyne. We report herein the first total synthesis and structural confirmation of the marine natural product (9R)-jamaicamide B.
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Cyanobacteria
Country/Region as subject:
Caribe ingles
/
Jamaica
Language:
En
Journal:
Org Biomol Chem
Journal subject:
BIOQUIMICA
/
QUIMICA
Year:
2024
Document type:
Article
Affiliation country:
Country of publication: