Thomas E. Klepach, Ph.D.

Affiliations: 
2008 University of Notre Dame, Notre Dame, IN, United States 
Area:
Oligosaccharides
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"Thomas Klepach"
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Anthony S. Serianni grad student 2008 Notre Dame
 (Integrated experimental and theoretical studies of saccharide structure.)
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Publications

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Klepach T, Zhao H, Hu X, et al. (2015) Informing saccharide structural NMR studies with density functional theory calculations. Methods in Molecular Biology (Clifton, N.J.). 1273: 289-331
Klepach TE, Reed M, Noll BC, et al. (2009) Methyl beta-allolactoside [methyl beta-D-galactopyranosyl-(1-->6)-beta-D-glucopyranoside] monohydrate. Acta Crystallographica. Section C, Crystal Structure Communications. 65: o601-6
Klepach T, Carmichael I, Serianni AS. (2008) 13C-labeled N-acetyl-neuraminic acid in aqueous solution: detection and quantification of acyclic keto, keto hydrate, and enol forms by 13C NMR spectroscopy. Journal of the American Chemical Society. 130: 11892-900
Klepach T, Zhang W, Carmichael I, et al. (2008) (13)C-(1)H and (13)C-(13)C NMR J-couplings in (13)C-labeled N-acetyl-neuraminic acid: correlations with molecular structure. The Journal of Organic Chemistry. 73: 4376-87
Bose-Basu B, Klepach T, Bondo G, et al. (2007) 13C-13C NMR spin-spin coupling constants in saccharides: structural correlations involving all carbons in aldohexopyranosyl rings. The Journal of Organic Chemistry. 72: 7511-22
Pan Q, Klepach T, Carmichael I, et al. (2005) 4J(COCCH) and 4J(CCCCH) as probes of exocyclic hydroxymethyl group conformation in saccharides. The Journal of Organic Chemistry. 70: 7542-9
Klepach TE, Carmichael I, Serianni AS. (2005) Geminal 2JCCH spin-spin coupling constants as probes of the phi glycosidic torsion angle in oligosaccharides. Journal of the American Chemical Society. 127: 9781-93
Thibaudeau C, Stenutz R, Hertz B, et al. (2004) Correlated C-C and C-O bond conformations in saccharide hydroxymethyl groups: parametrization and application of redundant 1H-1H, 13C-1H, and 13C-13C NMR J-couplings. Journal of the American Chemical Society. 126: 15668-85
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