Recent Advances in Total Synthesis of Tetrahydroisoquinoline Alkaloids Quinocarcin and Lemonomycin

Author:

Yang Yang1,Guo Ju1,Shen Lanhua1,Li Jingyi1,Li Fuan1,Wang Sifan1

Affiliation:

1. Key Laboratory of Green Chemical Engineering Process of Ministry of Education/Hubei Key Laboratory of Novel Reactor and Green Chemical Technology, Wuhan Institute of Technology

Abstract

Abstract: Tetrahydroisoquinoline natural products are a kind of alkaloids containing various pharmacological activities. These structurally diverse alkaloids mainly consist of two subclasses, monotetrahydroisoquinolines(MTHI) and bistetrahydroisoquinolines(BTHI). Since its family member, Ecteinascidin-743 (INN: Trabectedin, trade name: Yondelis® ), has been approved by European Union in 2007 and the FDA in 2015 for the treatment of advanced soft tissue tumors, the research on this kind of natural product is full of new vitality. Quinocarcin and lemonomycin share a common diazabicyclo[3.2.1]octane framework that belongs to the subclass of MTHI, and their excellent antitumor activity and challenging architecture have made them an ideal target for total synthesis. In this short review, the progress in the total synthesis of quinocarcin and lemonomycin is summarized.

Publisher

Bentham Science Publishers Ltd.

Subject

Organic Chemistry

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