Synthesis of polyhydroxylated 6-N-benzylpiperidin-2-ones. A novel access to 1,5-dideoxy-1,5-imino-D-xylitol

Article abstract of DOI:10.1080/00397919508012674

The synthesis of polyhydroxylated 6-N-benzylpiperidin-2-ones is described from the corresponding N-benzylaminoglycoside. These compounds are easily reduced to the differently protected 1,5-dideoxy-1,5-imino-D-xylitol.

Full text of DOI:10.1080/00397919508012674

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Synthetic Communications: An
International Journal for Rapid
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Organic Chemistry
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Synthesis of Polyhydroxylated
6-N-Benzylpiperidin-2-Ones. A
Novel Access to 1, 5-Dideoxy-1,
5-imino-D-xylitol
Francęois-Didier Boyer a , Ange Pancrazi b & Jean-
Yves Lallemand b
a INRA, Unité de Phytopharmacie et Médiateurs
Chimiques, CNRA, route de Saint-Cyr, 78026,
Versailles Cedex, France
b Laboratoire de Synthèse Organique, D.C.S.O. Ecole
Polytechnique, 91128, Palaiseau Cedex, France
Published online: 23 Sep 2006.
To cite this article: Francois-Didier Boyer , Ange Pancrazi & Jean-Yves Lallemand
(1995) Synthesis of Polyhydroxylated 6-N-Benzylpiperidin-2-Ones. A Novel Access to 1,
5-Dideoxy-1, 5-imino-D-xylitol, Synthetic Communications: An International Journal
for Rapid Communication of Synthetic Organic Chemistry, 25:8, 1099-1108
To link to this article: http://dx.doi.org/10.1080/00397919508012674
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