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- W2061143997 abstract "An efficient and mild Ni(ClO4)2-catalyzed [3+2] cycloaddition of N-tosylaziridines and aldehydesvia C–C bond cleavage was developed. The cycloaddition reaction proceeds with high diastereoselectivity and regioselectivity leading to highly substituted 1,3-oxazolidines. Notably, this novel reaction can be easily expanded to gram level scale and the thermal conditions cannot achieve the same transformation." @default.
- W2061143997 created "2016-06-24" @default.
- W2061143997 creator A5006928430 @default.
- W2061143997 creator A5048609660 @default.
- W2061143997 creator A5051482208 @default.
- W2061143997 date "2011-01-01" @default.
- W2061143997 modified "2023-10-07" @default.
- W2061143997 title "Nickel(ii)-catalyzed diastereoselective [3+2] cycloaddition of N-tosyl-aziridines and aldehydes via selective carbon–carbon bond cleavage" @default.
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- W2061143997 doi "https://doi.org/10.1039/c1cc12189h" @default.
- W2061143997 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/21655580" @default.
- W2061143997 hasPublicationYear "2011" @default.
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