1 research outputs found
Inherently Chiral Azonia[6]helicene-Modified β‑Cyclodextrin: Synthesis, Characterization, and Chirality Sensing of Underivatized Amino Acids in Water
The (<i>P</i>)- and (<i>M</i>)-3-azonia[6]helicenyl
β-cyclodextrins exhibit l/d selectivities
of up to 12.4 and <i>P</i>/<i>M</i> preferences
of up to 28.2 upon complexation with underivatized proteinogenic amino
acids in aqueous solution at pH 7.3