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

C.      Thomassigny; M.   T.   Barroso; C.      Greck

doi:10.2174/1570178054038876

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.

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

« Previous Next »

Rights & Permissions Print Cite

Letters in Organic Chemistry

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.

Export Options

Export File:

RIS (for EndNote, Reference Manager, ProCite)

BibTeX

Text

Content:

Citation Only

Citation and Abstract

About this article

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