Natural chirality of methylene sites applied to the recognition of origin and to the study of biochemical mechanisms
- 11 July 1983
- journal article
- Published by Wiley in FEBS Letters
- Vol. 158 (1) , 131-133
- https://doi.org/10.1016/0014-5793(83)80692-9
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Identification of the origin of natural alcohols by natural abundance hydrogen-2 nuclear magnetic resonanceAnalytical Chemistry, 1982
- A new method for the identification of the origin of natural products. Quantitative deuterium NMR at the natural abundance level applied to the characterization of anetholesJournal of the American Chemical Society, 1982
- Natural selective 2H labelling applied to the study of chemical mechanisms; labelling without enrichmentJournal of the Chemical Society, Chemical Communications, 1982
- Deuterium labelling at the natural abundance level as studied by high field quantitative 2H NMRTetrahedron Letters, 1981
- Determination of the enantiomeric purity and absolute configuration of α-deuteriated primary alcoholsJournal of the Chemical Society, Chemical Communications, 1973
- THE ABSOLUTE CONFIGURATION OFdextro-1-DEUTERIOETHANOLCanadian Journal of Chemistry, 1963
- Enzymatic Synthesis of the Enantiomorphis of Ethanol-1-d1,2Journal of the American Chemical Society, 1953