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- W2949352912 abstract "We have developed, on the basis of a chelation-strategy, an efficient copper-catalyzed aziridination protocol with the use of 5-methyl-2-pyridinesulfonamide and PhI(OAc)2. The reaction proceeds smoothly under mild conditions to give aziridines in moderate to good yields in the absence of external ligands or bases. The coordination-assisted approach offers the additional benefits that efficient deprotection of the N-substituent and selective aziridine ring-opening are effectively achieved." @default.
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- W2949352912 date "2004-09-30" @default.
- W2949352912 modified "2023-10-07" @default.
- W2949352912 title "Notable Coordination Effects of 2-Pyridinesulfonamides Leading to Efficient Aziridination and Selective Aziridine Ring Opening" @default.
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- W2949352912 doi "https://doi.org/10.1021/ol0481784" @default.
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