Programmed Polyene Cyclization Enabled by Chromophore Disruption.

J Am Chem Soc

Department of Chemistry and Biochemistry, Florida State University, Tallahassee, Florida 32306, United States.

Published: April 2022

A new polyene cyclization strategy exploiting β-ionyl derivatives was developed. Photoinduced deconjugation of the extended π-system within these chromophores unveils a contrathermodynamic polyene that engages in a Heck bicyclization to afford [4.4.1]-propellanes. This cascade improves upon the limited regioselectivity achieved using existing biomimetic tactics and tolerates both electron-rich and electron-deficient (hetero)aryl groups. The utility of this approach was demonstrated with the diverted total synthesis of taxodione and salviasperanol, two isomeric abietane diterpenes that were previously inaccessible along the same synthetic pathway.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10559755PMC
http://dx.doi.org/10.1021/jacs.2c02144DOI Listing

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