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J Org Chem ; 81(8): 3430-4, 2016 Apr 15.
Article in English | MEDLINE | ID: mdl-27002931

ABSTRACT

The (P)- and (M)-3-azonia[6]helicenyl ß-cyclodextrins exhibit L/D selectivities of up to 12.4 and P/M preferences of up to 28.2 upon complexation with underivatized proteinogenic amino acids in aqueous solution at pH 7.3.


Subject(s)
Amino Acids/chemical synthesis , Polycyclic Compounds/chemistry , beta-Cyclodextrins/chemistry , Amino Acids/chemistry , Stereoisomerism , Water
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