Catalytic asymmetric synthesis achieves efficient production of zephycitrine, suggesting new drug possibilities.
The first catalytic asymmetric total synthesis of the naturally occurring Amaryllidaceae alkaloid, (+)‐zephycitrine ( 1a ), has been accomplished. This efficient 11‐step route (8.3% overall yield) establishes the key stereocenters using an organocatalytic Corey–Itsuno reduction. The construction of the complex core structure, featuring three contiguous stereocenters, was subsequently realized via a Mitsunobu reaction and a microwave‐assisted intramolecular carbonyl‐ene reaction. The synthesis was completed with a final Pictet–Spengler cyclization. This concise approach, employing a sequence of classical and robust reactions, provides a versatile and efficient platform for accessing pro‐drug derivatives and other members of the Amaryllidaceae alkaloid family.
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Mondal et al. (2026) studied this question.
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