Stereopermutation on the Putative Structure of the Marine Natural Product Mucosin

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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Bibliographic Details
Main Authors: Simen G. Antonsen, Harrison Gallantree-Smith, Carl Henrik Görbitz, Trond Vidar Hansen, Yngve H. Stenstrøm, Jens M. J. Nolsøe
Format: Article
Language:English
Published: MDPI AG 2017-10-01
Series:Molecules
Subjects:
marine hydrindane natural product
asymmetric synthesis
stereodivergent strategy
structural elucidation
eicosanoid
Online Access:https://www.mdpi.com/1420-3049/22/10/1720

Internet

https://www.mdpi.com/1420-3049/22/10/1720

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