化学
对映选择合成
全合成
催化作用
纳米技术
甲烷氧化偶联
生化工程
组合化学
有机化学
工程类
材料科学
作者
Muhammad Usman,Xudong Hu,Wen‐Bo Liu
标识
DOI:10.1002/cjoc.202000029
摘要
Tetrahydrocarbazol‐4‐one represents a prevalent framework of numerous natural products and pharmaceuticals. This review summaries the recent synthetic progresses of this core structure, including Fischer indolization, oxidative and reductive coupling, α‐arylative cyclization by means of transition‐ metal catalysis or under metal‐free conditions, and other methods. The recently emerged enantioselective catalytic methods of tetrahydrocarbazol‐4‐ ones are also described. The mechanistic insights and applications of these strategies as a key step in the total (formal) synthesis of complex alkaloids are highlighted as well.
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