Concise Total Synthesis of Isospongian Diterpenoid (±)‐Polyrhaphin D

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Abstract
The first total synthesis of isospongian diterpenoid (±)‐polyrhaphin D has been accomplished in 9 steps with 19 % overall yield starting from the Wieland–Miescher ketone derivative. The key features of our synthesis include a sequential reduction/Michael addition/aldol condenzation to assemble the A ring and an intramolecular dehydrative cyclization/olefin isomerization reaction to install the γ‐butenolide D ring.

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