化学
对映选择合成
胺化
催化作用
对映体药物
硝基苯
产量(工程)
有机化学
组合化学
材料科学
冶金
作者
Tianjiao Cui,Chen‐Xi Ye,Jordan Thelemann,Daniel Jenisch,Eric Meggers
标识
DOI:10.1002/cjoc.202300162
摘要
Comprehensive Summary Enantioselective or enantioconvergent iron‐catalyzed ring‐closing C(sp 3 )‐H aminations of N ‐aroyloxyurea through intermediate iron nitrene species provide chiral 2‐imidazolidinones in up to 99% yield and with up to 95% ee (40 examples). This is a rare example in which sustainable iron catalysis is combined with C(sp 3 )‐H amination and asymmetric catalysis. Chiral 2‐imidazolidinones are prevalent structural motifs in bioactive molecules and can also be hydrolyzed to valuable chiral vicinal diamines in a single step.
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