Issue 12, 1999
From the journal:

Chemical Communications

Stereochemical course of the reduction step in the formation of 2-C-methylerythritol from the terpene precursor 1-deoxyxylulose in higher plants

Duilio Arigoni,   José-Luis Giner,   Silvia Sagner,   Juraithip Wungsintaweekul,   Meinhart H. Zenk,   Klaus Kis,   Adelbert Bacher  and  Wolfgang Eisenreich  

Abstract

Feeding of 1-deoxy-D-[3-2H]xylulose to leaves of the tree Liriodendron tulipifera affords 2-C-methyl-D-erythritollabelled specifically in the HSi position of C-1.

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Article information

DOI
https://doi.org/10.1039/A902216C
Article type
Paper

Chem. Commun., 1999, 1127-1128

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Stereochemical course of the reduction step in the formation of 2-C-methylerythritol from the terpene precursor 1-deoxyxylulose in higher plants

D. Arigoni, J. Giner, S. Sagner, J. Wungsintaweekul, M. H. Zenk, K. Kis, A. Bacher and W. Eisenreich, Chem. Commun., 1999, 1127 DOI: 10.1039/A902216C

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