Volume 127, Issue 21 pp. 6353-6357
Zuschrift

Catalytic Asymmetric Total Synthesis of (−)-Galanthamine and (−)-Lycoramine

Lei Li

Lei Li

State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Xue Yuan Rd. 38, Beijing 100191 (China)

These authors contributed equally to this work.

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Qiao Yang

Qiao Yang

State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Xue Yuan Rd. 38, Beijing 100191 (China)

These authors contributed equally to this work.

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Dr. Yuan Wang

Dr. Yuan Wang

State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Xue Yuan Rd. 38, Beijing 100191 (China)

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Prof. Yanxing Jia

Corresponding Author

Prof. Yanxing Jia

State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Xue Yuan Rd. 38, Beijing 100191 (China)

State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Xue Yuan Rd. 38, Beijing 100191 (China)Search for more papers by this author
First published: 02 April 2015
Citations: 21

We are grateful to the National Natural Science Foundation of China (Nos. 21402003, and 21290183) for their financial support.

Abstract

The catalytic asymmetric total syntheses of (−)-galanthamine (1) and (−)-lycoramine (2) have been achieved by using a conceptually new strategy featuring two metal-catalyzed reactions as the key steps. A new method for the construction of 3,4-fused benzofurans has been developed through a palladium-catalyzed intramolecular Larock annulation reaction, which was successfully applied to the construction of the ABD tricyclic skeleton of 1 and 2. To achieve the asymmetric synthesis of 1 and 2, a ScIII/N,N′-dioxide complex was used to catalyze the enantioselective conjugate addition of 3-alkyl-substituted benzofuranone to methyl vinyl ketone for the construction of a chiral quaternary carbon center.

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