Year: 2026
Type: article
Abstract: We disclose a concise, asymmetric synthesis of (-)-verrucarol, the natural product precursor of bioactive trichothecene macrocycles including verrucarins A and J. Historically, enantioselective construction of the 6/6/5 (A/B/C) ring system of the 12,13-epoxytrichothec-9-ene (EPT) core of trichothecene natural products has been a significant challenge. This architecture was constructed beginning with a chiral Lewis acid-catalyzed, enantioselective [4+2] cycloaddition to afford a cis-fused A/B ring fragment. A mechanistic hypothesis for the pivotal [4+2] cycloaddition was developed through experimentation and density functional theory (DFT). En route to completing the 6/6/5 core, we demonstrate diastereoselective modifications of the [4+2] cycloadduct including silylative generation and addition to a vinyl oxocarbenium. Final C-ring closure was achieved by a diastereoselective 5-endo-trig cyclization, thereby completing formal [3+2] annulation over two steps. Late-stage alkene transposition and hydroxyl-directed epoxidation furnished the target compound, (-)-verrucarol.
DOI: 10.1002/anie.5526474
Institution: Boston University
Language: English
Subfield: Organic Chemistry
Field: Chemistry
Domain: Physical Sciences
Open Access status: green
Awards: G1259630582, Acquisition of 300 & 400 MHz NMR Consoles, G4620400719, Acquisition of a Single Crystal X-ray Diffraction System for Macromolecular and Small Molecule Crytsallography, G7871885648, Acquisition of a High-Resolution Mass Spectrometer, G9000012602, Chemical Synthesis of Complex Natural Products for Translational Science
OpenAlex ID: W7134925898