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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.

PublisherTaylor & Francis
Reference styleAuthor–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 inAnalytical Chemistry and Chromatography Molecular spectroscopy and chirality Crystallography and molecular interactions DNA and Nucleic Acid Chemistry Spectroscopy and Quantum Chemical Studies
ISSN1024-2430
h-index13
i10-index18
Total citations468
Top institutions publishing hereHebrew University of Jerusalem
You getA submission-ready PDF and the editable LaTeX source — ready to submit.

Papers published in Enantiomer A Journal of Stereochemistry per year

1
1996
2
1997
1
1998
3
1999
1
2000
1
2001
48
2002

Citation impact of Enantiomer A Journal of Stereochemistry by publication year

1
1996
10
1997
9
1998
45
1999
0
2000
3
2001
400
2002

Citations each year’s papers have accumulated so far — the most recent years are still building up.

Most-cited papers in Enantiomer A Journal of Stereochemistry

Vibrational Circular Dichroism in the Near Infrared: Instrumental Developments and Applications

Ettore Castiglioni, France Lebon, Giovanna Longhi et al. · 1 Jul 2002

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…

The Supramolecular Structure of Self-Assembly Formed by Capsanthin Derivatives

Zsolt Bikádi, Ferenc Zsila, József Deli et al. · 1 Mar 2002

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…

Mechanistic Aspects of Chiral Discrimination on an Amylose Tris(3,5-dimethylphenyl)carbamate

Y. Bereznitski, Rosario LoBrutto, Narayan Variankaval et al. · 1 Nov 2002

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…

CD of Single-Stranded, Double-Stranded, and G-Quartet Nucleic Acids in Complexes with a Single-Stranded DNA-Binding Protein

Donald M. Gray, Carla W. Gray, Tung‐Chung Mou et al. · 1 Mar 2002

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…

Enantiomer A Journal of Stereochemistry template — frequently asked questions

How do I write a paper in the Enantiomer A Journal of Stereochemistry format?
In DocuGuru you write your manuscript in a normal editor — no LaTeX setup required — and select the Enantiomer A Journal of Stereochemistry template. When you export, DocuGuru compiles the paper into the official Taylor & Francis format and hands you a submission-ready PDF along with the editable LaTeX source.
What reference style does Enantiomer A Journal of Stereochemistry use?
Enantiomer A Journal of Stereochemistry uses Author–year (Chicago, T&F) references, shown as author–year markers such as (Smith, 2023) in the text. DocuGuru formats every in-text citation and the reference list in this exact style automatically. A reference appears like this: Smith, Ada, Ben Jones, and Cara Lee. 2023. "A Representative Article Title." Enantiomer A Journal of Stereochemistry 12 (3): 45–58.
Do I need to know LaTeX to submit to Enantiomer A Journal of Stereochemistry?
No. DocuGuru generates the interact LaTeX class and compiles the PDF for you in the background, so you get a Taylor & Francis-ready Enantiomer A Journal of Stereochemistry document without writing any LaTeX. If you do want it, the LaTeX source is included in the export.
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Who publishes Enantiomer A Journal of Stereochemistry?
Enantiomer A Journal of Stereochemistry is a multidisciplinary journal published by Taylor & Francis. DocuGuru's Enantiomer A Journal of Stereochemistry template matches Taylor & Francis's official submission format.
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