Selectively deuterated monomers for preparation of deuterated po 1 y ( ( dime t h y 1 i m i n i o ) prop y 1 e ne ) , p o 1 y ( ( d i m e t h y 1 i 10 i n i 0 ) hex y 1 c n e ) , and poly((dimethy1iminio)decylene) have been synthesized:(2-'Y2)-1.3-dibromopropane. ( 1.10-11 2 ) -, ( 2 , 9-2H2 I-,
Deuterium labelling of theaflavin
β Scribed by Weimin Peng; Yin-fang Yao
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- French
- Weight
- 123 KB
- Volume
- 52
- Category
- Article
- ISSN
- 0022-2135
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β¦ Synopsis
Abstract
An efficient deuterium labelling of theaflavin, aiming at radiolabelling of theaflavin, was accomplished for the first time by using 4βdeuteriumβlabelled epiβcatechin as the precursor and the resulting Dβlabelled theaflavin was fully characterized by ^1^H NMR, ^13^C NMR, IR spectroscopy and ESIβMS. The synthesis features a novel efficient polyphenol oxidase (PPO) catalyzed benzotropolone formation. PPO was bound onto a selected polymer by a novel efficient method developed in this lab. Copyright Β© 2009 John Wiley & Sons, Ltd.
π SIMILAR VOLUMES
N-Aryl amides may be deuterated by exchange with deuterium oxide in the presence of rhodium(fI1) chloride. Under such conditions deuterium is introduced into positions t o the anilide nitrogen atom with a high degree of regioselectivity.
Deuterium labelled thiomuscimol ( 6 ) was synthesized v i a zatalytic deuteration in strongly basic CZH302H-'H 0 (9:l) of 3-methoxy-4-bromo-5-(N-meth-oxycarbonyZaminomethy1) isothiazole ( 3 ) . ment of bromine by deuterium was accompanied by partial exchange of the side chain methylene protons for d
## Abstract Theaflavin, theaflavin monogallate and theaflavin digallate were isolated from black tea leaves and studied by 1D and 2D NMR techniques, thus allowing unambiguous assignment of the ^1^H and ^13^C resonances of these complexes. Earlier studies have not yielded ^13^C data of equal reliabi