Conversion of isoxazolines to β-hydroxy esters. Synthesis of 2-deoxy-D-ribose

doi:10.1016/S0040-4039(00)85028-5

Tetrahedron Letters

Volume 27, Issue 38, 1986, Pages 4647-4650

https://doi.org/10.1016/S0040-4039(00)85028-5 Get rights and content

Abstract

A simple and effficient preparation of β-hydroxy esters with a well-defined stereochemistry has been developed using 3-bromoisoxazolines as key-intermidiates. A synthesis of 2-decxy-D-ribose is also reported

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Conversion of isoxazolines to β-hydroxy esters. Synthesis of 2-deoxy-D-ribose

Abstract

Acc. Chem. Res.

The Tenth Int.Cong. of Heterocyclic Chem

A.C.S. Monograph 180

II Farmaco Ed. Sc.

II Farmaco Ed. Sc.

J. Am. Chem. Soc.

J. Org. Chem.