Issue 4, 1999

Diastereoselective Synthesis of N-Protected β-Amino-α-hydroxyacids (Norstatines) from Urethane N-Carboxyanhydrides (UNCAs)

Abstract

β-Amino-α-hydroxyacids (norstatines) are prepared from urethane N-protected carboxyanhydrides (UNCAs); the key step is the diastereoselective reduction of a keto-acetylenic compound, which lead is, with syn diastereoselectivity, to the corresponding propargylic alcohol.

Article information

Article type
Paper

J. Chem. Res. (S), 1999, 282-283

Diastereoselective Synthesis of N-Protected β-Amino-α-hydroxyacids (Norstatines) from Urethane N-Carboxyanhydrides (UNCAs)

P. Audin, C. Pothion, J. Fehrentz, A. Loffet, J. Martinez and J. Paris, J. Chem. Res. (S), 1999, 282 DOI: 10.1039/A809421G

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