Synthesis of new pseudonucleosides containing sulfamylated derivatives of natural amino acids as aglycone

Article abstract of DOI:10.1080/07328319908044724

New chiral sulfahydantoins have been synthesized via alkaline cyclisation, starting from symmetric sulfamide derivatives of natural amino acids. Tetraacetyl ribofuranose was used in the glycosylation step in order to obtain the pseudonucleosides in β-anom

Full text of DOI:10.1080/07328319908044724

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Nucleosides and Nucleotides
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Synthesis of New Pseudonucleosides
Containing Sulfamylated Derivatives of
Natural Amino Acids as Aglycone
Nour-Eddine Aouf a , Ouassila Attoui a & Abdelghani Djahoudi a
a Laboratory of Bioorganic Chemistry, Annaba University , BP12 El,
Hadjar, Algeria
Published online: 04 Oct 2006.
To cite this article: Nour-Eddine Aouf , Ouassila Attoui & Abdelghani Djahoudi (1999) Synthesis of
New Pseudonucleosides Containing Sulfamylated Derivatives of Natural Amino Acids as Aglycone,
Nucleosides and Nucleotides, 18:6-7, 1385-1386, DOI: 10.1080/07328319908044724
To link to this article: http://dx.doi.org/10.1080/07328319908044724
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