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Total Synthesis of (+)-7-Bromotrypargine and Unnatural Analogues: Biological Evaluation Uncovers Activity at CNS Targets of Therapeutic Relevance
[Image: see text] The first total synthesis of (+)-7-bromotrypargine, a β-carboline alkaloid from Ancornia sp. is reported. The synthesis proceeds in nine steps, eight steps longest linear sequence, in 36.9% overall yield. Biological characterization found that (+)-7-bromotrypargine is a H(3) antago...
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| Main Authors: | , , , , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
American Chemical Society
2011
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| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3254090/ https://ncbi.nlm.nih.gov/pubmed/22247792 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/cn200075n |
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