Application of stable isotope labelling methodology to the biosynthesis of the mycotoxin, terretonin, by aspergillus terreus: incorporation of 13C-labelled acetates and methionine, 2H- and 13C, 18O-labelled ethyl 3,5-dimethylorsellinate and oxygen-18 gas
暂无分享,去创建一个
[1] J. Vederas. The use of stable isotopes in biosynthetic studies. , 1987, Natural product reports.
[2] Richard N. Moore,et al. Biosynthesis of the hypocholesterolemic agent mevinolin by Aspergillus terreus. Determination of the origin of carbon, hydrogen, and oxygen atoms by carbon-13 NMR and mass spectrometry , 1985 .
[3] Y. Katsube,et al. STRUCTURE OF ED-1 ISOLATED FROM EMERICELLA DENTATA , 1982 .
[4] T. J. Simpson. Biosynthesis of highly modified meroterpenoids in aspergillus variecolor. Incorporation of 13C-labelled acetates and methionine into anditomin and andilesin C , 1981 .
[5] J. Vederas,et al. Magnitudes of 18O isotope shifts in 13C nuclear magnetic resonance spectra of ketones and alcohols , 1980 .
[6] J. Vederas. Structural dependence of oxygen-18 isotope shifts in carbon-13 NMR spectra , 1980 .
[7] C. Foote,et al. Acyclic mechanism in the cleavage of benzils with alkaline hydrogen peroxide , 1979 .
[8] R. J. Cole,et al. Austin, a novel polyisoprenoid mycotoxin from Aspergillus ustus. , 1976, Journal of the American Chemical Society.