| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5167558 | Phytochemistry | 2006 | 10 Pages |
Abstract
The deuterium patterns (the relative abundances of isotopomers) of natural aromatic compounds are determined by that of their precursors in the shikimic acid pathway - erythrose, PEP and NADPH - and by intramolecular (IIE) and kinetic (KIE) isotope effects accompanying the NIH-shift during hydroxylation by monooxygenases.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Hanns-Ludwig Schmidt, Roland A. Werner, Wolfgang Eisenreich, Claudio Fuganti, Giovanni Fronza, Gérald Remaud, Richard J. Robins,