Conformational study of the open-chain and furanose structures of d-erythrose and d-threose
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference45 articles.
1. DFTMD studies of glucose and epimers: anomeric ratios, rotamer populations, and hydration energies
2. Infrared and Raman spectra, conformational stability, ab initio calculations of structure, and vibrational assignment of α and β glucose
3. Conformational Properties of and a Reorientation Triggered by Sugar−Water Vibrational Resonance in the Hydroxymethyl Group in Hydrated β-Glucopyranose
4. Neutron diffraction and simulation studies of the exocyclic hydroxymethyl conformation of glucose
5. Stereoelectronic and Solvation Effects Determine Hydroxymethyl Conformational Preferences in Monosaccharides
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2. Erythrose and Threose: Carbonyl Migrations, Epimerizations, Aldol, and Oxidative Fragmentation Reactions under Plausible Prebiotic Conditions;Chemistry – A European Journal;2022-12-19
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