NMR as a tool for simultaneous study of diasteroisomeric inclusion complexes, part 2: complexes formed by racemic mixture of 4′-hydroxyflavanone and two cyclodextrins
Author:
Publisher
Springer Science and Business Media LLC
Subject
Condensed Matter Physics,General Chemistry,Food Science
Link
http://link.springer.com/content/pdf/10.1007/s10847-011-0094-4.pdf
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4. Kasprzyk-Hordern, B.: Pharmacologically active compounds in the environment and their chirality. Chem. Soc. Rev. 39, 4466–4503 (2010)
5. Anczewski, W., Dodziuk, H., Ejchart, A.: Manifestation of chiral recognition of camphor enantiomers by α-cyclodextrin in longitudinal and transverse relaxation rates of the corresponding 1:2 complexes and determination of the orientation of the guest inside the host capsule. Chirality 15, 654–659 (2003)
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