Advances in the Total Synthesis of Gelsemine

Author:

Yang Liyan1,Wang Zhonglei2ORCID

Affiliation:

1. School of Physics and Physical Engineering, Qufu Normal University, Qufu, 273165, P.R. China

2. Key Laboratory of Green Natural Products and Pharmaceutical Intermediates in Colleges and Universities of Shandong Province, Key Laboratory of Life-Organic Analysis of Shandong Province, School of Chemistry and Chemical Engineering, Qufu Normal University, Qufu, 273165, P.R. China | School of Pharmaceutical Sciences, Tsinghua University, Beijing 100084, P.R. China

Abstract

Abstract: Gelsemine is a remarkable indole alkaloid isolated from the medicinal plant Gelsemium elegans (Carolina or yellow jasmine) and demonstrates effectiveness in alleviating cognitive impairment, suggesting it could treat Alzheimer's disease. Gelsemine comprises seven adjoining chiral carbon centres and hexacyclic cage structures, making it an oddly difficult synthetic target. The unique structure and potential bio-pharmacological properties of gelsemine have led to the publication of nine interesting total syntheses of gelsemine (including three asymmetric syntheses) in the near past three decades by eight distinguished research groups. Several strategies are brimming with modern concepts of synthesis, such as highly enantioselective organocatalytic Diels–Alder reaction and the biomimetic enol–oxonium cyclization reaction. To better explore the therapeutic effects of gelsemine, this review summarizes the progress in the total synthesis tactics and strategies of the fascinating natural product gelsemine.

Funder

Qufu Normal University, China

Publisher

Bentham Science Publishers Ltd.

Subject

Organic Chemistry

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. A bioinspired cyclization toward koumine and gelsemine;Cell Reports Physical Science;2022-10

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