Preparation of 2,5-anhydrohexitols (part II). Intramolecular nucleophilic substitution of cyclic sulfates

Article abstract of DOI:10.1080/07328309908543990

The 2-O-acetyl-3,4-di-O-benzyl-5,6-O-cyclic sulfates 5, 16 and 25, derived from D-arabinose, D-ribose and D-xylose, respectively, are useful precursors in the synthesis of 2,5-anhydrohexitols. 5-Exo-tet cyclization of compounds 5, 16, and 25 under the inf

Full text of DOI:10.1080/07328309908543990

Journal of Carbohydrate Chemistry
ISSN: 0732-8303 (Print) 1532-2327 (Online) Journal homepage: http://www.tandfonline.com/loi/lcar20
Preparation of 2,5-Anhydrohexitols (Part Ii).
Intramolecular Nucleophilic Substitution of Cyclic
Sulfates
Floris L. van Delft , A. Rob , P.M. Valentijn , Gijs A. van der Marel & Jacques H.
van Boom
To cite this article: Floris L. van Delft , A. Rob , P.M. Valentijn , Gijs A. van der Marel & Jacques
H. van Boom (1999) Preparation of 2,5-Anhydrohexitols (Part Ii). Intramolecular Nucleophilic
Substitution of Cyclic Sulfates, Journal of Carbohydrate Chemistry, 18:2, 191-207, DOI:
10.1080/07328309908543990
To link to this article: http://dx.doi.org/10.1080/07328309908543990
Published online: 27 Feb 2008.
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Date: 01 June 2016, At: 05:56