ChemInform Abstract: Synthesis of Enantiomerically Pure 2,3‐Disubstituted Isoxazolidin‐5‐ones.

Irma Panfil; S. Maciejewski; C. BELZECKI; Marek Chmielewski

doi:10.1002/chin.198940205

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ChemInform Abstract: Synthesis of Enantiomerically Pure 2,3‐Disubstituted Isoxazolidin‐5‐ones.

Irma Panfil S. Maciejewski C. BELZECKI Marek Chmielewski

Year: 1989 Journal: ChemInform Vol: 20 (40) Publisher: Wiley

DOI: 10.1002/chin.198940205

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Abstract

Abstract The α,β‐unsaturated sugar lactones (I) react with the hydroxylamines (II) to give the optically pure 3‐(hydroxyalkyl)isoxazolidin‐5‐ones (III) which are characterized as acetates or silyl ethers.

Keywords:

Chemistry Silylation Organic chemistry Sugar Optically active Catalysis

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Carbohydrate Chemistry and Synthesis

Physical Sciences → Chemistry → Organic Chemistry

Chemical Synthesis and Analysis

Life Sciences → Biochemistry, Genetics and Molecular Biology → Molecular Biology

Synthetic Organic Chemistry Methods

Physical Sciences → Chemistry → Organic Chemistry

ChemInform Abstract: Synthesis of Enantiomerically Pure 2,3‐Disubstituted Isoxazolidin‐5‐ones.

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