Near infrared vibrational circular dichroism spectra in the region of 1300 to 800 nm were recorded for 12 enantiomeric pairs of molecules with a home-made dispersive apparatus. With respect to earlier measurements, a better signal-to-noise ratio was obtained, thus allowing a more precise determination of molecular parameters. A detailed examination of the spectra between 1300…
Enantiomer A Journal of Stereochemistry Template
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About the Enantiomer A Journal of Stereochemistry format
Enantiomer A Journal of Stereochemistry is a peer-reviewed journal published by Taylor & Francis, covering Analytical Chemistry and Chromatography, Molecular spectroscopy and chirality, Crystallography and molecular interactions.
| Publisher | Taylor & Francis |
|---|---|
| Reference style | Author–year (Chicago, T&F) Author–year — (Smith, 2023) in the text Smith, Ada, Ben Jones, and Cara Lee. 2023. "A Representative Article Title." Enantiomer A Journal of Stereochemistry 12 (3): 45–58.
Formats any DOI in Enantiomer A Journal of Stereochemistry style. No sign-up. |
| Publishes research in | Analytical Chemistry and Chromatography Molecular spectroscopy and chirality Crystallography and molecular interactions DNA and Nucleic Acid Chemistry Spectroscopy and Quantum Chemical Studies |
| ISSN | 1024-2430 |
| h-index | 13 |
| i10-index | 18 |
| Total citations | 468 |
| Top institutions publishing here | Hebrew University of Jerusalem |
| You get | A submission-ready PDF and the editable LaTeX source — ready to submit. |
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Most-cited papers in Enantiomer A Journal of Stereochemistry
Carotenoids form structured self-assembly upon aqueous dilution of their organic solutions. In order to test the proposal predicting carotenoid aggregates to be organized in closely packed H-type (card-pack) manner by intermolecular hydrogen bonds, the trihydroxy derivative of capsanthin (1), (6'R)-capsanthol (2) ((all-E,3R,3'S,5'R,6'R)-beta,kappa-carotene-3,3',6'-triol) was acetylated to obtain all varieties of mono-, di- and triacetates and the…
The separation of [2R-[2alpha(R*),3alpha]]-5-[[2-[1-[3,5-bis-(trifluoromethyl)phenyl]ethoxy]-3(S)-4-fluorophenyl)4-morpholinyl]-methyl]-N,N-dimethyl-1H-1,2,3-triazole-4-methanamine hydrochloride from its enantiomer was achieved on an amylose tris-3,5-dimethylphenyl carbamate stationary phase. The retention of the enantiomers is dominated by weak hydrogen bonds while the enantioselectivity is governed by other kinds of interactions, e.g., inclusion in the amylose carbamate chains. Van't Hoffplots of 1nalpha vs. reciprocal temperature were non-linear and…
We review CD studies of a single-stranded DNA binding protein, g5p, of the Ff group of bacterial viruses. The CD spectrum of the g5p is dominated by a positive tyrosine La band at 229 nm, to which all five of the protein tyrosines contribute. The La band becomes much less positive upon binding of g5p…