Total synthesis and isolation of citrinalin and cyclopiamine congeners

Article

关键词: ENANTIOSELECTIVE TOTAL-SYNTHESIS;    MARINE-DERIVED FUNGUS;    OXIDATION;    STEPHACIDIN;    METABOLITES;    DERIVATIVES;    ALKALOIDS;    CHEMISTRY;    SECONDARY;    REVISION;   

DOI  :  10.1038/nature13273

来源: SCIE

【 摘 要 】

Many natural products that contain basic nitrogen atoms-for example alkaloids like morphine and quinine-have the potential to treat a broad range of human diseases. However, the presence of a nitrogen atom in a target molecule can complicate its chemical synthesis because of the basicity of nitrogen atoms and their susceptibility to oxidation. Obtaining such compounds by chemical synthesis can be further complicated by the presence of multiple nitrogen atoms, but it can be done by the selective introduction and removal of functional groups that mitigate basicity. Here we use such a strategy to complete the chemical syntheses of citrinalin B and cyclopiamine B. The chemical connections that have been realized as a result of these syntheses, in addition to the isolation of both 17-hydroxycitrinalin B and citrinalin C (which contains a bicyclo[2.2.2]diazaoctane structural unit) through carbon-13 feeding studies, support the existence of a common bicyclo[2.2.2]diazaoctane-containing biogenetic precursor to these compounds, as has been proposed previously.

【 授权许可】

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