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Volumn 6, Issue 1-2, 1995, Pages 141-157

Recognition of sugars and related compounds by “reading-out”-type interfaces

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EID: 0000736478     PISSN: 10610278     EISSN: 10290478     Source Type: Journal    
DOI: 10.1080/10610279508032530     Document Type: Article
Times cited : (78)

References (72)
  • 7
  • 30
    • 0020202426 scopus 로고
    • For a comprehensive review see
    • For a comprehensive review see Wulff, G. Pure Appl. Chem. 1982, 54, 2093.
    • (1982) Pure Appl. Chem. , vol.54 , Issue.2093
    • Wulff, G.1
  • 31
    • 84954668626 scopus 로고    scopus 로고
    • From our work and that of others (references 9–30) it is known that the boronate ester is rapidly and reversibly formed under basic conditions. Noncovalent interactions are described using such terms as recognition, complex and binding constants
    • From our work and that of others (references 9–30) it is known that the boronate ester is rapidly and reversibly formed under basic conditions. Noncovalent interactions are described using such terms as “recognition”, “complex” and “binding constants”. These terms will be used to describe the equilibrium between covalent boronate ester and free boronic acid at high pH.
    • These terms will be used to describe the equilibrium between covalent boronate ester and free boronic acid at high pH
  • 36
    • 84954801497 scopus 로고    scopus 로고
    • In the CD studies of monosaccharides D-galactose frequently shows exceptional behaviours2
    • Here the discussions are made for the pyranose form but similar discussions are possible for the furanose form
    • In the CD studies of monosaccharides D-galactose frequently shows exceptional behaviours2. The reason is not well understood. Here the discussions are made for the pyranose form but similar discussions are possible for the furanose form.
    • The reason is not well understood
  • 54
    • 0003516958 scopus 로고
    • For a comprehensive review see, (ed by Inoue, Y.; Gokel, G. W.); Marcel Dekker: New York, chapter 9
    • For a comprehensive review see Shinkai, S. In Cation Binding by Macrocycles (ed by Inoue, Y.; Gokel, G. W.); Marcel Dekker: New York, 1990, chapter 9.
    • (1990) Cation Binding by Macrocycles
    • Shinkai, S.1
  • 69
    • 0000627623 scopus 로고
    • A solution containing cholesteryl nanoate
    • (1.2XIO-5 mol), cholesteryl chloride (0.8 XIO-5mol) and the 2:1 boronic acid saccharide complex (5.2 X10-7mol) in chloroform was prepared, An aliquot (200 mL) was spread on a quartz plate and mixed with minute glass beads having a uniform diameter (10±0.2mM). The sample was dried and then sandwitched between another quartz plate. The thickness of the sample prepared is then regulated by the glass beads. The wavelength of maximum reflection (XR = nP, where n is the mean index of reflection and P is the helical pitch of the cholesteric mesophase) was measured spectrophotometrically at 27°C. For details of the measurement method see
    • A solution containing cholesteryl nanoate (1.2XIO-5 mol), cholesteryl chloride (0.8 XIO-5mol) and the 2:1 boronic acid saccharide complex (5.2 X10-7mol) in chloroform was prepared. An aliquot (200 mL) was spread on a quartz plate and mixed with minute glass beads having a uniform diameter (10±0.2mM). The sample was dried and then sandwitched between another quartz plate. The thickness of the sample prepared is then regulated by the glass beads. The wavelength of maximum reflection (XR = nP, where n is the mean index of reflection and P is the helical pitch of the cholesteric mesophase) was measured spectrophotometrically at 27°C. For details of the measurement method see: Shannon, P. J. Macromolecules 1984, 17, 1873.
    • (1984) Macromolecules , vol.17 , Issue.1873
    • Shannon, P.J.1
  • 70
    • 84954754003 scopus 로고    scopus 로고
    • Energy minimizations of the 1/saccharide complexes was conducted using a semiempirical molecular orbital calculation method with full-geometry optimization (MOPAC ver. 6.0, AMI Hamiltonian).65
    • These calculations were preformed on the engineering workstation system (SUN 4/2 and IRIS 4D/35G). The illustrations in Figure 2 were made by the ORTEPC66 for the optimized structures
    • Energy minimizations of the 1/saccharide complexes was conducted using a semiempirical molecular orbital calculation method with full-geometry optimization (MOPAC ver. 6.0, AMI Hamiltonian).65 The imput structures for the complexes were established using the molecular modeling system (MOL-GRAPH ver3.0, Daikin Ind. Ltd.) These calculations were preformed on the engineering workstation system (SUN 4/2 and IRIS 4D/35G). The illustrations in Figure 2 were made by the ORTEPC66 for the optimized structures.
    • The imput structures for the complexes were established using the molecular modeling system (MOL-GRAPH ver3.0, Daikin Ind. Ltd.)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.