色胺
废止
化学
组合化学
立体化学
有机化学
生物化学
催化作用
作者
Luo-Rong Yuan,You Zi,Shun‐Jun Ji,Xiaoping Xu
标识
DOI:10.1021/acs.joc.4c02302
摘要
A mild approach for synthesizing CF3-substituted β-aza-spiroindolines and β-carbolines from tryptamine-derived isocyanides via site-selective radical annulations has been reported. The crucial role of C2 substituents in the selective annulation process has been clarified. The approach shows good generality and practical applicability, highlighting its effectiveness and versatility.
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