FR901483: Synthetic Efficiency Remains a Challenge

Author:

Ruan Zhuwei12,Li Cheng3,Shen Defeng12,Huang Sha-Hua14,Hong Ran1

Affiliation:

1. Key Laboratory of Synthetic Chemistry of Natural Substances, Center for Excellence in Molecular Synthesis, Shanghai Institute of Organic Chemistry (CAS)

2. University of Chinese Academy of Sciences

3. WuXi AppTec

4. School of Chemical and Environmental Engineering, Shanghai Institute of Technology

Abstract

FR901483 is a unique alkaloid bearing an aza-tricyclic structure, a phosphate group, and a congested tertiary nitrogen center. This alkaloid was reported to be a potent immunosuppressant with antimetabolite ability. The unprecedented architecture has captured imagination of synthetic chemists since its isolation in 1996. To date, ten total or formal syntheses and several synthetic approaches to access the tricyclic core skeleton have been reported. In this review, we highlight the novel synthetic methods and strategies and discuss the synthetic challenge for meeting the criteria of drug development.1 Introduction2 Bioinspired Total Synthesis of FR9014833 Non-bioinspired Approaches toward FR9014834 Various Tactics for Accessing the Core Skeleton5 Challenges for Efficiency

Funder

National Natural Science Foundation of China

Publisher

Georg Thieme Verlag KG

Subject

Organic Chemistry,Catalysis

Cited by 9 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. Aza-Wacker Cyclization Toward the Bridged Core of FR901483;Synthesis;2023-01-13

2. The phosphate ester group in secondary metabolites;Natural Product Reports;2022

3. A Bridge to Alkaloid Synthesis;The Chemical Record;2021-09-02

4. Reinventing the wheel for enabling the synthesis of hinckdentine A;Tetrahedron Letters;2021-03

5. (−)-FR901483 and TAN1251 (A-D);α-Tertiary Amines en Route to Natural Products;2021

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