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Sulfur Letters is a peer-reviewed journal published by Taylor & Francis, covering Sulfur-Based Synthesis Techniques, Synthesis and Characterization of Heterocyclic Compounds, Synthesis of heterocyclic compounds.
| 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." Sulfur Letters 12 (3): 45–58.
Formats any DOI in Sulfur Letters style. No sign-up. |
| Publishes research in | Sulfur-Based Synthesis Techniques Synthesis and Characterization of Heterocyclic Compounds Synthesis of heterocyclic compounds Chemical Synthesis and Reactions Organic Chemistry Cycloaddition Reactions |
| ISSN | 0278-6117 |
| h-index | 12 |
| i10-index | 19 |
| Total citations | 514 |
| Top institutions publishing here | A.E. Favorsky Irkutsk Institute of Chemistry |
| Journal website | www.tandfonline.com |
| You get | A submission-ready PDF and the editable LaTeX source — ready to submit. |
Citations each year’s papers have accumulated so far — the most recent years are still building up.
Condensation of 1,3-thiazolidinone derivatives 1a-c with different aromatic aldehydes and/or aryldiazonium chlorides gave the corresponding arylidenes 2-10 and arylazo-1,3-thiazolidinones 12-20. Bromination of 12 resulted in the formation of dibromo derivative 21. Treatment of 1a-c with HCHO-piperidine gave the Mannich adduct 24. Compound 1a was hydroxymethylated, oxidized and formylated to yield the products 25-28. The structures…
Reaction of substituted pyrazolin-5-one and 3-phenyl-5-isoxazolone 1a-c with phenyl isothiocyanate in basic DMF gave the non-isolable sodium salt of the adduct 2a-c which was treated with HCl to give the corresponding thiocarbamoyl derivatives 3a-c . The latter compounds underwent heterocyclization upon treatment with chloroacetyl chloride and ethyl bromoacetate to give the corresponding thiazolidinone derivatives 6…
Thiocarbamoyl derivatives (2a-c) were prepared in a good yield by a modified method. Their behavior toward aromatic diazonium salts, hydrazine hydrate and chloroacetyl chloride were investigated. The structures of the ring systems have been confirmed by analytical and spectral methods.
Synthesis and physico-chemical properties of some 5-arylidene-3-(2-biphenyl-4-yl-2-oxo-ethyl)- and 3-(4-bromo-benzyl)-4-thioxo-thiazolidin-2-ones, 5-arylidene-3-(4-chloro-benzyl)-4-thioxo- and 4-oxo-thiazolidin-2-ones and 2-arylidene-6-benzoyl-amino- or 6-amino-4 H -benzo[1,4]thiazin-3-ones are described. These arylidene thiazolidines and benzothiazines compounds were prepared by Knoevenagel condensation with benzaldehydes.
Reaction of 4-(phenoxathiin-2-yl)-1-oxy or mercaptophthalazines 2a,c with phthalyl or tosylamino acids 3 and 4 has been found to yield 5,6a-j . Hydrazinolysis of 5,6a-e furnished amino derivatives 5,6k-o . Some of the newly synthesized products were tested for their antimicrobial activities.
