Journal of Heterocyclic Chemistry Template
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About the Journal of Heterocyclic Chemistry format
Journal of Heterocyclic Chemistry is a peer-reviewed journal published by Wiley, covering Synthesis and Biological Evaluation, Synthesis and Characterization of Heterocyclic Compounds, Synthesis and biological activity.
| Publisher | Wiley |
|---|---|
| Reference style | Author–year (Chicago) Author–year — (Smith, 2023) in the text Smith, Ada, Ben Jones, and Cara Lee. 2023. "A Representative Article Title." Journal of Heterocyclic Chemistry 12 (3): 45–58.
Formats any DOI in Journal of Heterocyclic Chemistry style. No sign-up. |
| Publishes research in | Synthesis and Biological Evaluation Synthesis and Characterization of Heterocyclic Compounds Synthesis and biological activity Synthesis and Reactions of Organic Compounds Synthesis of heterocyclic compounds |
| ISSN | 0022-152X |
| Citation impact (2-yr) | 2.21 |
| h-index | 89 |
| i10-index | 8,475 |
| Total citations | 225,815 |
| Article processing charge | $3,090 |
| Top institutions publishing here | Laboratoire de Chimie Organique |
| Journal website | onlinelibrary.wiley.com |
| You get | A submission-ready PDF and the editable LaTeX source — ready to submit. |
Papers published in Journal of Heterocyclic Chemistry per year
Citation impact of Journal of Heterocyclic Chemistry by publication year
Citations each year’s papers have accumulated so far — the most recent years are still building up.
Most-cited papers in Journal of Heterocyclic Chemistry
Abstract Procedures involving condensation of o ‐phenylenediamines with carboxylic acids, and reaction of bifunctional alkyl halides with bifunctional nucleophiles are described. Syntheses are reported of 2,6‐bis‐(2‐benzimidazyl)‐pyridine, 1,3‐bis(2‐benzimidazyl)‐2‐thiapropane, 1,7‐bis(2‐benzimidazyl)‐2,6‐dithiaheptane, 2‐hydroxymethyl‐5,6‐dimethylbenzimidazole, 2‐chloromethyl‐5,6‐dimethylbenzimidazole hydrochloride, 1,7‐bis(5,6‐dimethyl‐2‐benzimidazyl)‐2,6‐dithiaheptane, 3,6‐bis(1‐pyrazolyl)pyridazine, 2‐(2‐hydroxy‐3‐methyl–phenyl)benzimidazole, 2‐(2‐hydroxyphenyl)benzimidazole, 5‐(2‐hydroxphenyl)‐3‐methyl‐1‐phenylpyrazole, 3(5)‐(2‐hydroxyphenyl)‐5(3)‐methylpyrazole, 3(5)‐(2‐hydroxyphenyl)‐5(3)‐phenylpyrazole, and 1,3‐bis((5‐methylpyridyl)imino)isoindoline.
Abstract The review presents the most elegant and promising set of synthetic routes for the synthesis of 2‐aminothiophenes by the Gewald reaction. Applications of this facile methodology to pharmaceuticals and dyestuffs have been demonstrated.
Abstract The synthesis of six unsymmetrically substituted tetraarylporphyrins is reported. The compounds prepared are 5‐(R),10,15,20‐tritolylporphyrins, where R = 2‐pyridyl, 3‐pyridyl, 4‐acet‐amido, and 2,3 or 4‐hydroxyphenyl. Four new tetrasubstituted tetraarylporphyrins (5,10,15,20‐tetra‐(R)‐porphyrin) are also reported, where R = 3‐pyridyl, 4‐acetylphenyl, 4‐hydroxyphenyl and 4‐butoxyphenyl. The proton nmr spectra of these porphyrins are presented.