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Crystal structures and chiral recognition of the diastereomeric salts prepared from 2-methoxy-2-(1-naphthyl)propanoic acid

โœ Scribed by Ichikawa, Akio; Ono, Hiroshi; Echigo, Takuya; Mikata, Yuji


Book ID
124166001
Publisher
Royal Society of Chemistry
Year
2011
Tongue
English
Weight
940 KB
Volume
13
Category
Article
ISSN
1466-8033

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Enantiomer separation of a powerful chir
โœ Krisztina Gyimesi-Forrรกs; Kazuaki Akasaka; Michael Lรคmmerhofer; Norbert M. Maier ๐Ÿ“‚ Article ๐Ÿ“… 2005 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 512 KB

The enantiodiscriminating potential of the weak anion exchange-type quinine-based chiral stationary phases (CSPs) for direct enantiomer separation of racemic 2-methoxy-2-(1-naphthyl)propionic acid (selectand, SA) was studied. The influence of structure variations of the selector (SO) in the carbamat