Qinghan Li, Lirong Han, Hui Zhou, Jinsong Hou, Xiaohao Shi
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引用次数: 0
Abstract
Indole[2,1-a]isoquinoline structures are widely present in many drug molecules and natural product molecules. Its derivatives have a wide range of physiological and pharmacological activities such as antibacterial, antiviral, anti-tumor,anti-cytostatic,anti-venom, and as an inhibitor of tubulin polymerization properties. They are also important intermediates in organic synthesis and structural units in drug synthesis. Therefore, indole[2,1-a]isoquinoline compounds have great application value in the pharmaceutical field. The study of its synthesis methods has also become an important research field of organic synthesis. At present, chemists have developed many efficient methods for synthesizing indole[2,1-a]isoquinoline derivatives. Thispaper reviews the research progress in the synthesis methods and application of indole[2,1-a]isoquinoline compounds in recent years, and representative examples and reaction mechanisms are discussed.
期刊介绍:
Advanced Synthesis & Catalysis (ASC) is the leading primary journal in organic, organometallic, and applied chemistry.
The high impact of ASC can be attributed to the unique focus of the journal, which publishes exciting new results from academic and industrial labs on efficient, practical, and environmentally friendly organic synthesis. While homogeneous, heterogeneous, organic, and enzyme catalysis are key technologies to achieve green synthesis, significant contributions to the same goal by synthesis design, reaction techniques, flow chemistry, and continuous processing, multiphase catalysis, green solvents, catalyst immobilization, and recycling, separation science, and process development are also featured in ASC. The Aims and Scope can be found in the Notice to Authors or on the first page of the table of contents in every issue.