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Volumn 28, Issue 5, 1996, Pages 458-464
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Diastereomeric differences of "pendant type" monosubstituted cyclodextrins, mono-[6-deoxy-6N(N′-formyl L- and D-phenylglycylamino)]-β-cyclodextrin in conformation and "induced-fit" behavior
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Author keywords
Cyclodextrin; Diastereomer; Flexible Arm; Inclusion Molecular Recognition; Induced Fit; Nuclear Magnetic Resonance; Weak Interaction
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Indexed keywords
AROMATIC COMPOUNDS;
CONFORMATIONS;
EMISSION SPECTROSCOPY;
MOLECULAR DYNAMICS;
MOLECULES;
NUCLEAR MAGNETIC RESONANCE;
SYNTHESIS (CHEMICAL);
CAPPED TYPE;
CHIRAL CARBON;
DIASTEREOMERIC DIFFERENCES;
FORMYL GROUP;
HYDROPHOBIC CAVITY SHAPE;
MACROCYCLIC RING;
MOLECULAR RECOGNITION;
MONO DEOXY CYCLODEXTRIN;
MONO DEOXY FORMYL PHENYLGLYCYLAMINO CYCLODEXTRIN;
PENDANT TYPE;
MONOMERS;
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EID: 0029708048
PISSN: 00323896
EISSN: None
Source Type: Journal
DOI: 10.1295/polymj.28.458 Document Type: Article |
Times cited : (9)
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References (13)
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