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- W2053233722 abstract "The authors report enantio- and diastereoselective one-pot procedures to 4,5-disubstituted isoxazoline N-oxides having up to three contiguous stereocenters. The cascade reaction consists of an enantioselective, organocatalytic functionalization to α-bromo aldehydes or α,β-epoxy aldehydes, followed by a base mediated face-selective Henry reaction, and a subsequent stereospecific intramolecular O-alkylation. The obtained 4,5-disubstituted isoxazoline N-oxides are converted into l-ribo-phytosphingosine and polyhydroxylated α-amino acids." @default.
- W2053233722 created "2016-06-24" @default.
- W2053233722 date "2009-07-23" @default.
- W2053233722 modified "2023-09-26" @default.
- W2053233722 title "Molecular Complexity by Organocatalytic One-Pot Strategies" @default.
- W2053233722 doi "https://doi.org/10.1055/s-0029-1217596" @default.
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