The synthesis of isotopically labelled N-acetylcysteamine thioesters utilising a baker's yeast reduction in D2O
- 31 December 1991
- journal article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 1 (4) , 223-226
- https://doi.org/10.1016/s0960-894x(00)80257-7
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Intact incorporation of acetate-derived di- and tetraketides during biosynthesis of dehydrocurvularin, a macrolide phytotoxin from Alternaria cinerariaeJournal of the American Chemical Society, 1990
- Baker's Yeast as a Reagent in Organic SynthesisSynthesis, 1990
- Macrolide biosynthesis. 5. Intact incorporation of a chain-elongation intermediate into nargenicinJournal of the American Chemical Society, 1988
- Macrolide biosynthesis. 4. Intact incorporation of a chain-elongation intermediate into erythromycin.Journal of the American Chemical Society, 1987
- Macrolide biosynthesis. Tylactone formation involves the processive addition of three carbon unitsJournal of the American Chemical Society, 1987
- YEAST REDUCTION OF ETHYL ACETOACETATE: (S)-( + )-ETHYL 3-HYDROXYBUTANOATEOrganic Syntheses, 1985
- Synthesis of (2S)-2-PropylthietanAustralian Journal of Chemistry, 1982
- The Biosynthesis of Long-Chain Fatty Acids. Incorporation of Radioactivity from Stereospecifically Tritiated Malonyl Thiol Esters, and the Stereochemistry of the Acetyl-CoA Carboxylase ReactionEuropean Journal of Biochemistry, 1977
- .alpha.-Methoxy-.alpha.-trifluoromethylphenylacetic acid, a versatile reagent for the determination of enantiomeric composition of alcohols and aminesThe Journal of Organic Chemistry, 1969
- Über den Abbau der Aminosäuren bei der Hefegärung.Hoppe-Seyler´s Zeitschrift Für Physiologische Chemie, 1910