Issue 15, 1984
From the journal:

Journal of the Chemical Society, Chemical Communications

Biosynthesis of 6-methylsalicylic acid; the combined use of mono- and tri-duteriated acetate precursors to investigate the degree of stereocontrol in the aromatisation sequence

Chris Abell  and  James Staunton  

Abstract

The Results from a novel combination of incorporation experiments using mono- and tri-deuteriated acetate precursors indicate that the aromatisation sequence in 6-methylsalicylic acid biosynthesis occurs stereospecifically and therefore is under enzymic control.

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Article information

DOI
https://doi.org/10.1039/C39840001005
Article type
Paper

J. Chem. Soc., Chem. Commun., 1984, 1005-1007

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Biosynthesis of 6-methylsalicylic acid; the combined use of mono- and tri-duteriated acetate precursors to investigate the degree of stereocontrol in the aromatisation sequence

C. Abell and J. Staunton, J. Chem. Soc., Chem. Commun., 1984, 1005 DOI: 10.1039/C39840001005

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