Inherently Chiral Azonia[6]helicene-Modified β-Cyclodextrin: Synthesis, Characterization, and Chirality Sensing of Underivatized Amino Acids in Water
Helicene
Chirality
Characterization
DOI:
10.1021/acs.joc.6b00130
Publication Date:
2016-03-22T18:10:15Z
AUTHORS (12)
ABSTRACT
The (P)- and (M)-3-azonia[6]helicenyl β-cyclodextrins exhibit L/D selectivities of up to 12.4 P/M preferences 28.2 upon complexation with underivatized proteinogenic amino acids in aqueous solution at pH 7.3.
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