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Highly efficient regioselective ring openings of N-tosylaziridines to haloamines using ferric(Ⅲ) halides 被引量:1

Highly efficient regioselective ring openings of N-tosylaziridines to haloamines using ferric(Ⅲ) halides
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摘要 FeX3(X = Cl, Br) were found to be very effective reagents and powerful catalysts for regioselective ring openings of a variety of N-tosylaziridines with them to afford the corresponding b-haloamines in good to excellent yields with high regioselectivity under mild conditions. At the same time, 13 new compounds were obtained firstly. Moreover, the b-bromoamine prepared could be transferred into b-nitroamine with NaNO2 in moderate yield. FeX3(X = Cl, Br) were found to be very effective reagents and powerful catalysts for regioselective ring openings of a variety of N-tosylaziridines with them to afford the corresponding b-haloamines in good to excellent yields with high regioselectivity under mild conditions. At the same time, 13 new compounds were obtained firstly. Moreover, the b-bromoamine prepared could be transferred into b-nitroamine with NaNO2 in moderate yield.
出处 《Chinese Chemical Letters》 SCIE CAS CSCD 2014年第8期1174-1178,共5页 中国化学快报(英文版)
基金 the Natural Science Foundation of Shanxi Province (Nos. 2012021007-2, 2011011010-2) for financial support supported by Scientific and Technological Innovation Programs of Higher Education Institutions in Shanxi (No. 20120006)
关键词 RING-OPENING N-Tosylaziridine Haloamine Ferric (Ⅲ) halide Regioselectivity Ring-opening N-Tosylaziridine Haloamine Ferric (Ⅲ) halide Regioselectivity
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参考文献30

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