Synthesis of the Reported Structure of <i>trans</i>-Africanan-1α-ol
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A trisubstituted cyclopentane chiron has been prepared by dynamic kinetic reduction of a pulegone-derived β-keto ester. This chiron served as the starting material for the synthesis of the reported structure of the tricyclic sesquiterpene trans-africanan-1α-ol. The synthetic material was not congruent with the natural product.
创建时间：
2011-12-02
