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Total Synthesis of 6-Hydroxymetatacarboline-d Discovered from Mycena metata via the Pictet–Spengler Reaction Followed by the Horner–Wadsworth–Emmons Reaction
[Image: see text] Total synthesis of a new β-carboline alkaloid, 6-hydroxymetatacarboline-d, which was isolated from fruiting bodies of Mycena metata was accomplished in 14 steps. The synthetic strategy features the Pictet–Spengler reaction to construct the tricyclic core followed by amide coupling...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8028005/ https://www.ncbi.nlm.nih.gov/pubmed/33842763 http://dx.doi.org/10.1021/acsomega.0c06202 |
Sumario: | [Image: see text] Total synthesis of a new β-carboline alkaloid, 6-hydroxymetatacarboline-d, which was isolated from fruiting bodies of Mycena metata was accomplished in 14 steps. The synthetic strategy features the Pictet–Spengler reaction to construct the tricyclic core followed by amide coupling and the Horner–Wadsworth–Emmons reaction. |
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