Stereopermutation on the Putative Structure of the Marine Natural Product Mucosin

A stereodivergent total synthesis has been executed based on the plausibly misassigned structure of the unusual marine hydrindane mucosin (1). The topological connectivity of the four contiguous all-carbon stereocenters has been examined by selective permutation on the highlighted core. Thus, capita...

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Detalles Bibliográficos
Autores principales: Antonsen, Simen G., Gallantree-Smith, Harrison, Görbitz, Carl Henrik, Hansen, Trond Vidar, Stenstrøm, Yngve H., Nolsøe, Jens M. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151738/
https://www.ncbi.nlm.nih.gov/pubmed/29027970
http://dx.doi.org/10.3390/molecules22101720

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151738/
https://www.ncbi.nlm.nih.gov/pubmed/29027970
http://dx.doi.org/10.3390/molecules22101720

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