The use of quasi-enantiomeric isotopomers as chiral probes for determining stereoisomeric purity

This review discusses the use of chiral isotopomers, in particular the use of quasi‐enantiomeric isotopomers as novel chiral probes for determination of enantio‐ and diastereoisomeric purity. Copyright © 2004 John Wiley & Sons, Ltd.

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Published in:Journal of labelled compounds & radiopharmaceuticals 2004-09, Vol.47 (10), p.705-717
Main Authors: Eames, Jason, Suggate, Michael J.
Format: Article
Language:English
Subjects:
[13C]-labelling
[2H]-labelling
acyl transfer
Biological and medical sciences
Chemistry
Contrast media. Radiopharmaceuticals
covalent nucleophilic catalysis
diastereoisomeric excess
enantiomeric excess
Exact sciences and technology
isotopomers
Kinetics and mechanisms
Medical sciences
Organic chemistry
parallel kinetic resolution
Pharmacology. Drug treatments
quasi-enantiomers
Reactivity and mechanisms
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container_title Journal of labelled compounds & radiopharmaceuticals
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description This review discusses the use of chiral isotopomers, in particular the use of quasi‐enantiomeric isotopomers as novel chiral probes for determination of enantio‐ and diastereoisomeric purity. Copyright © 2004 John Wiley & Sons, Ltd.
doi_str_mv 10.1002/jlcr.860
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identifier ISSN: 0362-4803
ispartof Journal of labelled compounds & radiopharmaceuticals, 2004-09, Vol.47 (10), p.705-717
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source Wiley-Blackwell Read & Publish Collection
subjects [13C]-labelling
[2H]-labelling
acyl transfer
Biological and medical sciences
Chemistry
Contrast media. Radiopharmaceuticals
covalent nucleophilic catalysis
diastereoisomeric excess
enantiomeric excess
Exact sciences and technology
isotopomers
Kinetics and mechanisms
Medical sciences
Organic chemistry
parallel kinetic resolution
Pharmacology. Drug treatments
quasi-enantiomers
Reactivity and mechanisms
title The use of quasi-enantiomeric isotopomers as chiral probes for determining stereoisomeric purity
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