Metallocyclodextrins of 6A-(3-aminopropylamino)-6A-deoxy-β-cyclodextrin: their formation and enantioselective complexation of (R)- and (S)-tryptophan anions in aqueous solution
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Physical and Theoretical Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/1994/FT/FT9949000739
Reference20 articles.
1. The inclusion of the enantiomers of N-trifluoroacetyl-4-fluorophenylalanine and N-trifluoroacetylphenylalanine by cyclomaltohexaose: A 2H- and 19F-N.M.R. study
2. Chiral molecular recognition: a19F nuclear magnetic resonance study of the diastereoisomer inclusion complexes formed between fluorinated amino acid derivatives and α-cyclodextrin in aqueous solution
3. Substituent effects and chiral discrimination in the complexation of benzoic, 4-methylbenzoic and (RS)-2-phenylpropanoic acids and their conjugate bases by β-cyclodextrin and 6A-amino-6A-deoxy-β-cyclodextrin in aqueous solution: potentiometric titration and1H nuclear magnetic resonance spectroscopic study
4. Artificial receptors for amino acids in water. Local environmental effect on polar recognition by 6A-amino-6B-carboxy- and 6B-amino-6A-carboxy-.beta.-cyclodextrins
5. Deuterium relaxation time of?-d-tryptophan included in cyclodextrin host molecules
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