Synthesis of the bis-tetrahydropyrano[2,3-b:2′,3′-e] piperazine ring system: A new tricyclic heterocycle from D-glucosamine

Article abstract of DOI:10.1080/07328309608005676

2-Amino-3,4,6-tri-O-benzyl-2-deoxy-D-glucopyranose was transformed into its bis(tetrahydropyranyl)piperazine dimer (4) by reaction with 1,1′-thionyldiimidazole or 1,1′-sulfonyldiimidazole. This dimeric form of glucosamine is the first representative of th

Full text of DOI:10.1080/07328309608005676

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Synthesis of the Bis-
Tetrahydropyrano[2,3-b:2′,3′-e]
Piperazine Ring System: A New Tricyclic
Heterocycle from D-Glucosamine
Robert J. Kerns a , Toshihiko Toida a & Robert J. Linhardt a
a Division of Medicinal and Natural Products Chemistry , College of
Pharmacy University of Iowa , Iowa City, Iowa , 52242
Published online: 22 Aug 2006.
To cite this article: Robert J. Kerns , Toshihiko Toida & Robert J. Linhardt (1996) Synthesis of the
Bis-Tetrahydropyrano[2,3-b:2′,3′-e] Piperazine Ring System: A New Tricyclic Heterocycle from D-
Glucosamine, Journal of Carbohydrate Chemistry, 15:5, 581-590, DOI: 10.1080/07328309608005676
To link to this article: http://dx.doi.org/10.1080/07328309608005676
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