Structure of cyclodextrins and their complexes. Part 7. [1]. Unusual NMR manifestations of chiral recognition of (1R,5R)- and (1S,5S)-α-pinenes by α-cyclodextrin in different solvents

Polish Journal of Chemistry

Volumn 70, Issue 10, 1996, Pages 1361-1364

  Dodziuk, H ^a   Sitkowski, J ^a   Stefaniak, L ^a   Sybilska, D ^a  

^a POLISH ACADEMY OF SCIENCES   (Poland)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0041164403     PISSN: 01375083     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (23)

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2. Former parts of the series: Dodziuk H., Sitkowski J., Stefaniak L., Sybilska D. and Jurczak J., Part 5 : Supramol. Chem., 7, 33 (1996) ; Dodziuk H., Sitkowski J., Stefaniak L., Sybliska D., Jurczak J. and Chmurski K., Part 6 : Supramol. Chem., submitted for publication.
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6. (1R,5R)-α-pinene is (+)-α-pinene. As discussed in Ref. 5, we believe that chirality sense should be denoted on the basis of the modified version of the Cahn, Ingold, and Prelog classification of chirality [6].
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