Enantiospecific Aluminum-Catalyzed (3+2) Cycloaddition of Unactivated Aziridines with Isothiocyanates
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https://figshare.com/articles/dataset/Enantiospecific_Aluminum-Catalyzed_3_2_Cycloaddition_of_Unactivated_Aziridines_with_Isothiocyanates/4037883
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资源简介：
An Al(salen)Cl efficiently catalyzed
the enantiospecific (3+2)
cycloaddition of unactivated chiral aziridines with isothiocyanates
to furnish functionalized iminothiazolidines at room temperature with
94–99% ee. The use of an aluminum Lewis acid as the catalyst,
high enantiomeric purities, mild reaction conditions, broad substrate
scope, and the high atom economy are the significant practical features.
创建时间：
2016-11-14
