D/L selective re-binding of saccharide-imprinted [60]fullerene- bisadducts based on a saccharide-boronic acid interaction: Development of a molecular imprinting technique useful in a homogeneous system

Tetrahedron

Volumn 55, Issue 13, 1999, Pages 3883-3892

  Ishi i, Tsutomu ^a   Iguchi, Ritsuko ^a   Shinkai, Seiji ^a  

^a JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

BORONIC ACID DERIVATIVE; CARBOHYDRATE; FULLERENE DERIVATIVE;

ARTICLE; BINDING AFFINITY; CHEMICAL REACTION; MOLECULAR INTERACTION; MOLECULAR RECOGNITION; PRIORITY JOURNAL; STEREOCHEMISTRY;

EID: 0033605897     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(99)00117-9     Document Type: Article

References (23)

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16. fA), the three signs, f, C, and A mean fullerene, clockwise, and anticlockwise, respectively. For naming of chiral fullerene derivatives see: Thilgen, C.; Herrmann, A.; Diederich, F. Helv. Chim. Acta, 1997, 80, 183-199.
17. fA)-5. The CD spectra of 5a and 5b were already reported in reference 6b.
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22. Although the elemental analyses of 3 and 4 were also measured, the observed values did not coincided with the calculated values because of the contamination of a trace amount of solvents. Further, for 4 the existence of a few different structures such as free boronic acid, boronic acid anhydride, and cyclic trimer 2,4,6-o-triarylboroxin may cause the disagreement in elemental analysis. The high resolution mass spectrometry of 3 and 4 could not be performed because of the very low intensities of the parent ion peaks of 3 and 4.
23. 1H NMR spectroscopic method.