A New Hydrogen-Bonding Motif for Chiral Recognition in the Diastereomeric Salts of Racemic 1-Phenylethylamine Derivatives with Enantiopure O -Ethyl Phenylphosphonothioic Acid

Factors determining the pattern of a hyd

Factors determining the pattern of a hydrogen-bonding network in the diastereomeric salts of 1-arylethylamines with enantiopure P-chiral acids

✍ Yuka Kobayashi; Hiroaki Handa; Jin Maeda; Kazuhiko Saigo 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 370 KB

## Abstract In order to clarify factor(s) determining the pattern of a hydrogen‐bonding network in the diastereomeric salts of 1‐arylethylamines (**1**) with enantiopure P‐chiral acids, three kinds of enantiopure P‐chiral alkylphenylphosphinothioic acids (**3**) were synthesized, and their chiral r