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- W2026367088 abstract "Aziridination of cyclohex-2-enol, 3-methylcyclohex-2-enol, and 3-phenylcyclohex-2-enol with 3-acetoxyamino-2-ethylquinazolin-4(3H)-one (4) proceeds with high stereoselectivity syn to the hydroxy group to give compounds (7), (19), and (21), respectively in good yields. These results are analogous to the epoxidations of these alkenes using peracids. Aziridinations of cyclohex-2-enyl acetate or cyclohex-2-enyl methyl ether proceed stereospecifically anti to the acetoxy or methoxy group to give (11) and (17), respectively, but in low yield. These results are in contrast to the epoxidations of these alkenes using peracids." @default.
- W2026367088 created "2016-06-24" @default.
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- W2026367088 date "1989-01-01" @default.
- W2026367088 modified "2023-09-23" @default.
- W2026367088 title "Aziridination of cyclohex-2-enols and 3-substituted cyclohexenes: comparison with epoxidation" @default.
- W2026367088 doi "https://doi.org/10.1039/p19890001515" @default.
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