A cyclic sulfate approach to the synthesis of 1,4-dideoxy-1,4-imino derivatives of L-xylitol, L-arabinitol and D-xylitol

Article abstract of DOI:10.1080/00397919208020496

Polyhydroxylated pyrrolidines are readily accessible by ring opening of a 1,4-cyclic sulfate function in pentitol derivatives by nitrogen nucleophiles and further processing of the in situ generated charged sulfate group.

Full text of DOI:10.1080/00397919208020496

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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A Cyclic Sulfate Approach
to the Synthesis of 1,4-
Dideoxy-1,4-imino Derivatives
of L-Xylitol, L-Arabinitol and D-
Xylitol
Pieter A.M. van der Klein a , Wim Filemon a , Helgo
J.G. Broxterman a , Gijs A. van der Marel a &
Jacques H. van Boom a
a Gorlaeus Laboratories, P.O. Box 9502, 2300, RA,
Leiden, The Netherlands
Published online: 23 Sep 2006.
To cite this article: Pieter A.M. van der Klein , Wim Filemon , Helgo J.G.
Broxterman , Gijs A. van der Marel & Jacques H. van Boom (1992): A Cyclic Sulfate
Approach to the Synthesis of 1,4-Dideoxy-1,4-imino Derivatives of L-Xylitol, L-
Arabinitol and D-Xylitol, Synthetic Communications: An International Journal for
Rapid Communication of Synthetic Organic Chemistry, 22:12, 1763-1771
To link to this article: http://dx.doi.org/10.1080/00397919208020496
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