Issue 18, 1982

Application of 2H β-isotopic shifts in 13C n.m.r. spectra to biosynthetic studies. Incorporation of [1-13C, 2H3]acetate into O-methylasparvenone in Aspergillus parvulus

Abstract

Incorporation of [1-13C,2H3]acetate into O-methylasparvenone (1) and analysis of the 2H β-isotope shifts in the resulting 13C n.m.r. spectrum indicate that one hydrogen is lost from the methyl derived from the acetate ‘starter’ unit; the magnitude of the observed 2H β-isotope shifts showed a marked dependence on the functionality of the reporter 13C nucleus and the stereospecificity of 2H incorporation.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1982, 1074-1076

Application of 2H β-isotopic shifts in 13C n.m.r. spectra to biosynthetic studies. Incorporation of [1-13C, 2H3]acetate into O-methylasparvenone in Aspergillus parvulus

T. J. Simpson and D. J. Stenzel, J. Chem. Soc., Chem. Commun., 1982, 1074 DOI: 10.1039/C39820001074

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