(R)-O-Aryllactic acids: Convenient chiral solvating agents for direct 1H NMR determination of the enantiomeric composition of amines and amino alcohols
✍ Scribed by Rafael Chinchilla; Francisco Foubelo; Carmen Nájera; Miguel Yus
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 176 KB
- Volume
- 6
- Category
- Article
- ISSN
- 0957-4166
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
Enantiomers of t-butylphenylphosphinothioic acid were found to be useful chiral solvating agents (CSAs) for 1H-NMR determination of enantiomeric excess (ee) of many classes of chiral organic compounds, such as alcohols, diols, thiols, mercaptoalcohols, amines, amlnoalcohols, hydroxyacids and related
Permethylated Cyclodextrins as Chiral Solvating Agents for the Determination of the Enantiomeric Composition of Apolar Substrates by NMR. -Ongoing studies show the efficiency of permethylated β-cyclodextrin for the title purpose with racemic compounds such as (I) and (II). Additionally, the usefulne