JOURNAL BROWSE
Search
Advanced SearchSearch Tips
Synthesis and Conformational Analysis of Novel Polymeric Ligands based on myo-Inositol
facebook(new window)  Pirnt(new window) E-mail(new window) Excel Download
 Title & Authors
Synthesis and Conformational Analysis of Novel Polymeric Ligands based on myo-Inositol
Kim, Tae-Hyeon; Holmes, Andrew B.;
  PDF(new window)
 Abstract
Synthesis of novel polymeric ligands based on myo-inositol was performed. Cyclopolymerization, whose mechanism and the cyclic structure were proved, was first attempted to build a conformationally rigid inositol polymer. Comparative spectroscopic methods were introduced to verify the conformation of the prepared cyclohexane polymers. A conformationally rigid polymeric ligand was successfully prepared using myo-inositol carbonate.
 Keywords
myo-Inositol;Conformationally Rigid Polymer;Metal-binding Ligand;Conformational Analysis of Cyclohexane Polymers
 Language
Korean
 Cited by
1.
Conformational analysis of the natural iron chelator myo-inositol 1,2,3-trisphosphate using a pyrene-based fluorescent mimic, Organic & Biomolecular Chemistry, 2010, 8, 12, 2850  crossref(new windwow)
2.
Conformational study of the natural iron chelator myo-inositol 1,2,3-trisphosphate using restrained/flexible analogues and computational analysis, Tetrahedron, 2010, 66, 46, 8949  crossref(new windwow)
3.
Fluorescent probe: complexation of Fe3+with the myo-inositol 1,2,3-trisphosphate motif, Chemical Communications, 2008, 41, 5161  crossref(new windwow)
 References
1.
Wulff, G. Angew. Chem. Int. Ed. Engl. 1989, 28, 21 crossref(new window)

2.
Kaliyappan, T.; Kanna, P. Prog. Polym. Sci. 2000, 25, 343 crossref(new window)

3.
Schulz, G. E.; Schirmer, R. H. Principles of Protein Structure; Springer-Verlag; New York, 1979

4.
Angyal, S. J. Pure Appl. Chem. 1973, 35, 131 crossref(new window)

5.
Angyal, S. J. Tetrahedron, 1974, 30, 1695 crossref(new window)

6.
Angyal, S. J.; Greeves, D.; Littlemore, L. Aust. J. Chem. 1985, 38, 1561 crossref(new window)

7.
Anderson, J. E.; Angyal, S. J.; Craig, D. C. J. Chem. Soc. Perkin Trans. 2, 1997, 729

8.
Angyal, S. J. Aust. J. Chem. 2000, 53, 567 crossref(new window)

9.
Angyal, S. J. Carbohydr. Res. 2000, 325, 313 crossref(new window)

10.
Ghisletta, M.; Jalett, H. P.; Gerfin, T.; Gramlich, V.; Hegetschweiler, K. Helv. Chim. Acta, 1992, 75, 2233 crossref(new window)

11.
Kradolfer, T.; Hegetschweiler, K. Helv. Chim. Acta, 1992, 75, 2243 crossref(new window)

12.
Hegetschweiler, K.; Ghisletta, M.; Fassler, T. F.; Nesper, R.; Schmalle, H. W.; Rihs, G. Inorg. Chem. 1993, 32, 2032 crossref(new window)

13.
Tae, J.; Rogers, R. D.; Paquette, L. A. Org. Lett. 2000, 2, 139 crossref(new window)

14.
Paquette, L. A.; Tae, J. J. Am. Chem. Soc. 2001, 123, 4974 crossref(new window)

15.
Paquette, L. A.; Selvaraj, P. R.; Keller, K. M.; Brodbelt, J. S. Tetrahedron, 2005, 61, 231 crossref(new window)

16.
Kim, T.-H.; Dokolas, P.; Feeder, N.; Giles, M.; Holmes, A. B. Chem. Commun. 2000, 2419

17.
Kim, T.-H.; Giles, M.; Holmes, A. B. Chem. Commun. 2000, 2421

18.
Lee, H.-J.; Kim, T.-H. Bull. Korean Chem. Soc. 2006, 27, 359 crossref(new window)

19.
Corey, E. J.; Suggs, J. W. J. Org. Chem. 1973, 38, 3224 crossref(new window)