Issue 13, 1988

Biosynthesis of a carbocyclic pentose analogue linked to bacteriohopanetetrol from the bacterium Methylobacterium organophilum

Abstract

The labelling patterns resulting from incorporations of [1-13C]- and [2-13C]-acetate into a novel carbocyclic pentofuranose analogue linked via an ether bond to bacteriohopanetetrol in several bacteria were consistent with a reaction sequence starting from a 2-ketohexose and identical with those involved in the conversion of D-glucose into myo-inositol.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1988, 868-870

Biosynthesis of a carbocyclic pentose analogue linked to bacteriohopanetetrol from the bacterium Methylobacterium organophilum

G. Flesch and M. Rohmer, J. Chem. Soc., Chem. Commun., 1988, 868 DOI: 10.1039/C39880000868

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