Collect. Czech. Chem. Commun.
2003, 68, 1007-1019
https://doi.org/10.1135/cccc20031007
On the Conformation of Glycobilirubin
Stefan E. Boiadjiev and David A. Lightner*
Chemistry Department, University of Nevada, Reno, Nevada 89557-0020 U.S.A.
References
1. J. Parenteral Enteral Nutr. 1998, 22, 393.
< J. C.: https://doi.org/10.1177/0148607198022006393>
2. J. Lipid Res. 1992, 33, 617.
A. F., Mysels K. J.:
3. Falk Symp. Adv. Glucuronide Conjugation 1985, 245.
A. F., Palmer K. R., Yoon Y. B., Hagey L. R., Gurantz D., Huijghebaert S., Converse J. L., Cecchetti S., Michelotti E.:
4. Hepatology 1990, 12, 6S.
D. W., Carey M. C.:
5. Ann. Med. 1968, 12, 66.
G.:
6. Xenobiotica 1978, 8, 253.
< J. R., Millburn P., Williams R. T.: https://doi.org/10.3109/00498257809056147>
7. Chowdury J. R., Wolkoff A. W., Chowdury N. R., Arias I. M. in: The Metabolic and Molecular Bases of Inherited Disease (C. R. Scriver, A. L. Beaudet, W. S. Sly and D. Valle, Eds), Vol. 2, p. 3063. McGraw–Hill, New York 2001.
8. McDonagh A. F. in: The Porphyrins (D. Dolphin, Ed.), Vol. 6, p. 293. Academic Press, New York 1979.
9a. J. Gastroenterol. Hepatol. 1999, 14, 578.
< T., Tazuma S., Yamashita G., Kajiyama G.: https://doi.org/10.1046/j.1440-1746.1999.01917.x>
9b. Am. J. Physiol. 1993, 265, G445.
P. L. M., van Klinken J. W., van Gelder M., Ottenhoff R., Elferink R. P. J. O.:
10. Hoppe-Seyler’s Z. Physiol. Chem. 1958, 311, 87.
< M., Večerek B.: https://doi.org/10.1515/bchm2.1958.311.1.87>
11. J. Am. Chem. Soc. 1992, 114, 10123.
< S. E., Person R. V., Puzicha G., Knobler C., Maverick E., Trueblood K. N., Lightner D. A.: https://doi.org/10.1021/ja00052a006>
12. J. Am. Chem. Soc. 1995, 117, 8727.
< S. E., Anstine D. T., Lightner D. A.: https://doi.org/10.1021/ja00139a005>
13. Armarego W. L. F., Perrin D. D.: Purification of Laboratory Chemicals, 4th ed. Butterworth–Heinemann, Oxford (U.K.) 1996.
14. Tetrahedron: Asymmetry 1993, 4, 491.
< S. E., Person R. V., Lightner D. A.: https://doi.org/10.1016/S0957-4166(00)86092-9>
15. J. Heterocycl. Chem. 1994, 31, 707.
< N., Katayama H, Nisyiyama S., Ogawa T.: https://doi.org/10.1002/jhet.5570310402>
16. Monatsh. Chem. 2003, 134, 51.
< S. E., Lightner D. A.: https://doi.org/10.1007/s00706-002-0511-x>
17. Synthesis 1992, 328.
< D. P., Puzicha G., Lightner D. A.: https://doi.org/10.1055/s-1992-26102>
18. Tetrahedron: Asymmetry 1995, 6, 901.
< S. E., Anstine D. T., Lightner D. A.: https://doi.org/10.1016/0957-4166(95)00098-A>
19. Tetrahedron: Asymmetry 1999, 10, 607.
< S. E., Lightner D. A.: https://doi.org/10.1016/S0957-4166(99)00037-3>
20. J. Am. Chem. Soc. 1994, 116, 42.
< R. V., Peterson B. R., Lightner D. A.: https://doi.org/10.1021/ja00080a006>
21a. J. Am. Chem. Soc. 2000, 122, 11328.
< S. E., Lightner D. A.: https://doi.org/10.1021/ja002069c>
21b. Tetrahedron: Asymmetry 1999, 10, 2535.
< S. E., Lightner D. A.: https://doi.org/10.1016/S0957-4166(99)00254-2>
22. J. Chem. Soc., Chem. Commun. 1976, 122.
< P., Monti D.: https://doi.org/10.1039/c39760000122>
23. Isr. J. Chem. 1983, 23, 177.
< D., Navon D.: https://doi.org/10.1002/ijch.198300026>
24. Harada N., Nakanishi K.: Circular Dichroic Spectroscopy – Exciton Coupling in Organic Stereochemistry. University Science Books, Mill Valley (CA) 1983.
25. J. Am. Chem. Soc. 1987, 109, 6354.
< D. A., Gawronski J. K., Wijekoon W. M. D.: https://doi.org/10.1021/ja00255a020>
26. Tetrahedron 1997, 53, 14547.
< S. E., Pfeiffer W. P., Lightner D. A.: https://doi.org/10.1016/S0040-4020(97)01066-1>