Beckmann rearrangement and Baeyer-Villiger oxidation of N-benzyl-2-C:1-N-carbonyl-2-deoxy-5,6-O-isopropylidene-3-keto-α-D- ribofuranosylamine

Article abstract of DOI:10.1080/07328309708006510

N-Benzyl-2-C:1-N-carbonyl-2-deoxy-5,6-O-isopropylidene-3-keto-α-D- ribohexo-furanosylamine (5), available by [2+2]cycloaddition of trichloroacetyl isocyanate to 1,4-anhydro-3-O-benzyl-5,6-O-isopropylidene-D-arabino-hex-1-enitol (1), was subjected to Baeye

Full text of DOI:10.1080/07328309708006510

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Journal of Carbohydrate Chemistry
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Beckmann Rearrangement and
Baeyer-Villiger Oxidation of N-
Benzyl-2-C:1-N-Carbonyl-2-Deoxy-5,6-
O-Isopropylidene-3-Keto-α-d-
Ribofuranosylamine
Wojciech Abramski a , Zofia Urbanczyk-Lipkowska a & Marek
Chmielewski a
a Institute of Organic Chemistry, Polish Academy of Sciences ,
01-224, Warsaw, Poland
Published online: 21 Aug 2006.
To cite this article: Wojciech Abramski , Zofia Urbanczyk-Lipkowska & Marek Chmielewski (1997)
Beckmann Rearrangement and Baeyer-Villiger Oxidation of N-Benzyl-2-C:1-N-Carbonyl-2-Deoxy-5,6-O-
Isopropylidene-3-Keto-α-d-Ribofuranosylamine, Journal of Carbohydrate Chemistry, 16:1, 63-74
To link to this article: http://dx.doi.org/10.1080/07328309708006510
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