Absolute Configurations of Spiroiminodihydantoin and Allantoin Stereoisomers: Comparison of Computed and Measured Electronic Circular Dichroism Spectra
Author:
Affiliation:
1. Departments of Biology and Chemistry, New York University, New York, New York 10003
Publisher
American Chemical Society (ACS)
Subject
Toxicology,General Medicine
Link
https://pubs.acs.org/doi/pdf/10.1021/tx900107q
Reference36 articles.
1. Chiroptical Spectroscopic Determination of Molecular Structures of Chiral Sulfinamides: t-Butanesulfinamide
2. Determination of the absolute stereochemistry of chiral biphenanthryls in solution phase using chiroptical spectroscopic methods: 2,2′-Diphenyl-[3,3′-biphenanthrene]-4,4′-diol
3. Determination of the Absolute Configuration of [32](1,4)Barrelenophanedicarbonitrile Using Concerted Time-Dependent Density Functional Theory Calculations of Optical Rotation and Electronic Circular Dichroism
4. Why is it important to simultaneously use more than one chiroptical spectroscopic method for determining the structures of chiral molecules?
5. Absolute Configuration of Conformationally Flexiblecis-Dihydrodiol Metabolites by the Method of Confrontation of Experimental and Calculated Electronic CD Spectra and Optical Rotations
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