Stereoselective Preparation of 1-Deoxy-Homonojirimycin from a β- Ketoester Bearing Sugar

Title: Stereoselective Preparation of 1-Deoxy-Homonojirimycin from a β- Ketoester Bearing Sugar

Volume: 2 Issue: 4

Author(s): C. Thomassigny, M. T. Barroso and C. Greck

Affiliation:

Keywords: xylofuranose, deoxy-homonojirimycin, polyhydroxylated piperidine, ketoester, hydroxyester

Abstract: We present in this note the preparation of 1,5,6-trideoxy-1,5-imino-D-gluco-heptitol commonly known as 1-deoxy-homonojirimycin by a diastereoselective way. The polyhydroxylated piperidine has been obtained from a β-ketoester bearing a xylofuranose moiety.

Cite this article as:

Thomassigny C., Barroso T. M. and Greck C., Stereoselective Preparation of 1-Deoxy-Homonojirimycin from a β- Ketoester Bearing Sugar, Letters in Organic Chemistry 2005; 2 (4) . https://dx.doi.org/10.2174/1570178054038876