立体中心
对映选择合成
烷基化
筑地反应
化学
催化作用
吲哚试验
背景(考古学)
组合化学
有机化学
立体化学
古生物学
生物
作者
Marco Bandini,Astrid Eichholzer,Achille Umani‐Ronchi
标识
DOI:10.2174/157019307780599270
摘要
Indole benzylic stereocenters are molecular frameworks largely present in natural occurring compounds, with their absolute configuration being of key importance in determining the biological activity of the entire molecule. In this context, the development of new catalytic asymmetric strategies for their preparation is a research area of astonishingly rapid growth by means of organic as well as organometallic catalysts. Here, an update of this thriving scenario is presented by focusing in highly stereocontrolled Michael addition approaches, addition to carbonyl units, direct aromatic C-H activation/alkylation, and allylic alkylation. Keywords: Alkylation, asymmetric catalysis, Friedel-Crafts, indoles
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