An Enantiospecific Synthesis of Isoneoamphilectane Confirms Its Strained Tricyclic Structure

We describe a total synthesis of the rare isocyanoterpene natural product isoneoamphilectane and two of its unnatural diastereomers. The significantly strained ring system of the reported natural product-along with a hypothesis about a biosynthetic relationship to related family members-inspired us to consider a potential misassignment in the structure's relative configuration. As a result, we initially targeted two less strained, more accessible, stereoisomers of the reported natural product. When these compounds failed to exhibit spectroscopic data that matched those of isoneoamphilectane, we embarked on a synthesis of the originally proposed strained structure via an approach that hinged on a challenging cis-to-trans decalone epimerization. Ultimately, we implemented a novel cyclic sulfite pinacol-type rearrangement to generate the strained ring system. Additional features of this work include the application of a stereocontrolled Mukaiyama-Michael addition of an acyclic silylketene acetal, an unusual intramolecular alkoxide-mediated regioselective elimination, and an HAT-mediated alkene hydroazidation to forge the C-N bond of the tertiary isonitrile. Throughout this work, our synthetic planning was heavily guided by computational analyses to inform on key issues of stereochemical control.

Automated summary

We have successfully synthesized the rare isocyanoterpene natural product isoneoamphilectane and its two unnatural diastereomers. Our initial hypothesis about a misassignment in the structure's relative configuration led us to target two less-strained stereoisomers, but they did not match the spectroscopic data of isoneoamphilectane. We then embarked on a challenging synthesis of the originally proposed strained structure, guided by computational analyses to control stereochemistry.