Journal of the Chemical Society. Chemical communications p. 2051 - 2052 (1994)
Update date:2022-08-11
Topics:
Eliseev, Alexey V.
Iacobucci, Guillermo A.
Khanjin, Nikolai A.
Menger, F. M.
Spectroscopic and kinetic studies of β-cyclodextrin-linked L- and D-phenylalanine cyanoethyl esters in aqueous solution reveal an unusual intramolecular complexation mode where the hydrophobic portion of the amino acid resides outside the host cavity; L- and D-derivatives show different binding geometries and energies.
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