The 1 H and 13 C NMR chemical shift assignments of 10-substituted decal-2-ones, cis (H, CH 3 and CO 2 CH 3 ) and trans (H, CH 3 , OH and CO 2 C 2 H 5 ) were based on 2D COSY and HETCOR experiments, supported by selective spin decoupling experiments. The discrimination between the cis and the trans c
cis–trans isomerization of 2-(4-pyridyl)-substituted thiazolidine-4-carboxylic acids: pH dependence by 1H and 13C NMR
✍ Scribed by Fabio Ponticelli; Enrico Marinello; Maria Cristina Missale
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- English
- Weight
- 200 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The presence of two diastereoisomeric thiazolidines obtained by the reaction of L‐cysteine or L‐cysteine ethyl ester and pyridoxal or pyridoxal‐5‐phosphate is demonstrated by ^1^H and ^13^CNMR spectroscopy. Fast interconversion of isomers occurs in neutral or alkaline solution.
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