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oai:www.ideals.illinois.edu:2142/84481 2023-07-11 col_2142_5131 col_2142_14789 com_2142_5130 com_2142_14788 com_2142_8903

Petillo, Peter A. Flugge, Lisa Ann 2015-09-25T22:14:45Z 2015-09-25T22:14:45Z 10000-01-01 2000 2000 To better understand the interaction of water with hyaluronan, two uronic acids, beta-methyl glucuronic acid and beta-methyl galacturonic acid, were prepared, and their hydroxyl protons were studied using low temperature NMR. These results were compared to calculations of proton exchange in uronic acids. Calculations suggest that OH4 in glucuronic acid should exchange with solvent, whereas in galacturonic acid it should not. The NMR observations confirm the calculated predictions. Made available in DSpace on 2015-09-25T22:14:45Z (GMT). No. of bitstreams: 2 license.txt: 4848 bytes, checksum: 96035ab3f5e1c23cc7138a224ce498bd (MD5) 9989998.pdf: 7748292 bytes, checksum: 6c54c6d952de49b3577d9051aa561589 (MD5) Previous issue date: 2000 Embargo set by: Seth Robbins for item 85762 Lift date: Forever Reason: Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs U of I Only 192 p. Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 2000. http://hdl.handle.net/2142/84481 (MiAaPQ)AAI9989998 eng Chemistry, Organic Studies on Polysaccharide Synthesis and Solution Behavior text Chemistry Chemistry University of Illinois at Urbana-Champaign Dissertation Ph.D.