Jump to main content
Jump to site search

Issue 15, 1984
Previous Article Next Article

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

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.

Back to tab navigation

Article type: Paper
DOI: 10.1039/C39840001005
Citation: J. Chem. Soc., Chem. Commun., 1984, 1005-1007
  •   Request permissions

    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

Search articles by author

Spotlight

Advertisements