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Syntheses of specifically labelled 2,3,6-trideoxyhexoses

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Original languageEnglish
Pages (from-to)2297-2304
Number of pages8
JournalTetrahedron
Volume51
Issue number8
Publication statusPublished - 20 Feb 1995
Externally publishedYes

Abstract

Two synthetic approaches producing L-(-) and D-(+)-rhodinose (6 and 13 respectively), L-(-)-(19)- and D-(+)-amicetose and L- and D-enopyranose 15 specifically deuterated at C-2 and C-3 are described. The strategy which starts from threonine also offers the opportunity for the synthesis of the [1-13C]-labelled compounds.

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Syntheses of specifically labelled 2,3,6-trideoxyhexoses. / Kirschning, Andreas; Hary, Ulrike; Ries, Monika.
In: Tetrahedron, Vol. 51, No. 8, 20.02.1995, p. 2297-2304.

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Kirschning A, Hary U, Ries M. Syntheses of specifically labelled 2,3,6-trideoxyhexoses. Tetrahedron. 1995 Feb 20;51(8):2297-2304. doi: 10.1016/0040-4020(94)01081-A
Kirschning, Andreas ; Hary, Ulrike ; Ries, Monika. / Syntheses of specifically labelled 2,3,6-trideoxyhexoses. In: Tetrahedron. 1995 ; Vol. 51, No. 8. pp. 2297-2304.
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AU - Ries, Monika

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