A simple access to carbocyclic analogs of 2-deoxy-D-ribose having the 3-hydroxymethylene moiety replaced by heteroatoms

Article abstract of DOI:10.1080/07328309608005664

(2S,4S)-1-O-Benzyl-2,5-di-O-mesyl-4-O-methoxymethylpentan-1,2,4,5-tetrol, a versatile precursor for subsequent cyclisations with bivalent nucleophiles, was obtained in five steps from the easily accessible (3S,5S)-3-hydroxy-5-hydroxymethyldihydrofuran-2(3

Full text of DOI:10.1080/07328309608005664

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Journal of Carbohydrate Chemistry
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A Simple Access to Carbocyclic Analogs
of 2-Deoxy-d-Ribose Having the 3-
Hydroxymethylene Moiety Replaced by
Heteroatoms
Karsten Schürrle a & Wolfgang Piepersberg a
a FB 9- Chemische Mikrobiologie , Bergische Universität/GH ,
Gaußstr. 20, 42097, Wuppertal, Germany
Published online: 22 Aug 2006.
To cite this article: Karsten Schürrle & Wolfgang Piepersberg (1996) A Simple Access to Carbocyclic
Analogs of 2-Deoxy-d-Ribose Having the 3-Hydroxymethylene Moiety Replaced by Heteroatoms,
Journal of Carbohydrate Chemistry, 15:4, 435-447, DOI: 10.1080/07328309608005664
To link to this article: http://dx.doi.org/10.1080/07328309608005664
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