Asymmetric Total Synthesis of (2<i>R</i>)‑Hydroxynorneomajucin, a Norsesquiterpene from <i>Illicium jiadifengpi</i>

We report the first total synthesis of (2R)-hydroxy­norneomajucin, a norsesquiterpene derived from the Illicium genus. This natural product displays neurotrophic properties. Small molecule neurotrophins have potential as therapeutics in neurodegenerative diseases. Key steps of our synthesis include a Tsuji–Trost reaction, a Pauson–Khand cyclization, and a Nagata hydrocyanation. A simple sequence of reductions and a Mukaiyama hydration introduce the A-ring substituents with the correct configurations. The overall synthesis was completed in 17 steps (longest linear sequence, LLS).