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- W2884562244 endingPage "4448" @default.
- W2884562244 startingPage "4444" @default.
- W2884562244 abstract "Stereospecific Cu-catalyzed nucleophilic ring opening of N-sulfonylaziridines with propargylamines and subsequent hydroamination afford piperazines, which leads to double-bond isomerization to furnish tetrahydropyrazines. Optically active aziridines can be cross-coupled with high enantiomeric purities (>98% ee)." @default.
- W2884562244 created "2018-08-03" @default.
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- W2884562244 date "2018-07-16" @default.
- W2884562244 modified "2023-10-18" @default.
- W2884562244 title "Stereospecific Ring Opening and Cycloisomerization of Aziridines with Propargylamines: Synthesis of Functionalized Piperazines and Tetrahydropyrazines" @default.
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- W2884562244 doi "https://doi.org/10.1021/acs.orglett.8b01723" @default.
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