Issue 10, 1987

An elimination–rearrangement of ribulose-1,5-bisphosphate with implications for riboflavin biosynthesis

Abstract

Ribulose-1,5-bisphosphate (5) undergoes a sequence of elimination and benzilic acid rearrangement in a process with features that parallel those of the rearrangement occuring during incorporation of pentose precursors into riboflavin (1).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1987, 742-744

An elimination–rearrangement of ribulose-1,5-bisphosphate with implications for riboflavin biosynthesis

D. H. G. Crout and J. A. Hadfield, J. Chem. Soc., Chem. Commun., 1987, 742 DOI: 10.1039/C39870000742

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