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- W2022681108 abstract "Moreover, chiral selenideand diselenides containing ligands offer attractive and practical options in the development of asymmetric transformations. In this context, a straightforward synthesis of a new set of chiral β-seleno amine through a stereoselective aziridine ring opening with selenium nucleophiles, generated by reducing agents such as NaBH4, LiBHEt3, zinc or indium salts have been described by our group 2 . We herein report an ecofriendly procedure for the synthesis of chiral β-seleno amine under mild conditions, using selenium nucleophile generated by base in the presence of CuO nanopowder as a catalyst in ionic liquid BMIM[BF4] as solvent." @default.
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- W2022681108 date "2013-09-01" @default.
- W2022681108 modified "2023-09-27" @default.
- W2022681108 title "Copper Oxide Nanoparticles-Catalyzed Aziridine Ring Opening with Diaryl Diselenides Under Ionic Liquid as Reaction Medium" @default.
- W2022681108 doi "https://doi.org/10.5151/chempro-14bmos-r0026-1" @default.
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