Works matching IS 0022152X AND DT 2022 AND VI 59 AND IP 1
Results: 16
Design, synthesis, and biological evaluations of (E)‐2‐(1‐[2‐mercapto‐4‐methyl‐1‐phenyl‐1H‐imidazol‐5‐yl]ethylidene)hydrazinecarbothioamide derivatives as antimicrobial agents.
- Published in:
- Journal of Heterocyclic Chemistry, 2022, v. 59, n. 1, p. 178, doi. 10.1002/jhet.4378
- By:
- Publication type:
- Article
Thallium(III) p‐tosylate‐mediated oxidative [1,2] rearrangement of 2‐naphthyl and 2‐heteroarylchromanones.
- Published in:
- Journal of Heterocyclic Chemistry, 2022, v. 59, n. 1, p. 172, doi. 10.1002/jhet.4377
- By:
- Publication type:
- Article
Highly efficient microwave‐assisted solvent free sequential one‐pot multicomponent synthesis of novel 2‐hydroxy indenopyridin‐5‐ones and mechanismic computational study.
- Published in:
- Journal of Heterocyclic Chemistry, 2022, v. 59, n. 1, p. 161, doi. 10.1002/jhet.4375
- By:
- Publication type:
- Article
Design and synthesis of highly oxygenated furo[3,2‐c]pyran‐4‐ones and furo[3,2‐c]chromen‐4‐ones scaffold as anticancer and antimicrobial agents.
- Published in:
- Journal of Heterocyclic Chemistry, 2022, v. 59, n. 1, p. 144, doi. 10.1002/jhet.4374
- By:
- Publication type:
- Article
CuI/L‐proline‐catalyzed synthesis of bis(2‐(4,5‐diaryl‐1H‐imidazol‐2‐yl)phenyl)sulfane derivatives using potassium ethylxanthate as a sulfur source.
- Published in:
- Journal of Heterocyclic Chemistry, 2022, v. 59, n. 1, p. 67, doi. 10.1002/jhet.4365
- By:
- Publication type:
- Article
Synthesis, crystal structure, and DFT study of 4‐(2‐Chlorobenzyl)‐1‐(furan‐2‐yl)‐[1,2,4]triazolo[4,3‐a]quinazolin‐5(4H)‐one.
- Published in:
- Journal of Heterocyclic Chemistry, 2022, v. 59, n. 1, p. 137, doi. 10.1002/jhet.4373
- By:
- Publication type:
- Article
Benzimidazole based derivatives as anticancer agents: Structure activity relationship analysis for various targets.
- Published in:
- 2022
- By:
- Publication type:
- Literature Review
A solvent‐free manganese(II) ‐catalyzed Clauson‐Kaas protocol for the synthesis of N‐aryl pyrroles under microwave irradiation.
- Published in:
- Journal of Heterocyclic Chemistry, 2022, v. 59, n. 1, p. 194, doi. 10.1002/jhet.4372
- By:
- Publication type:
- Article
Total synthesis of xylapeptide B [Cyclo‐(L‐Leu‐L‐Pro‐N‐Me‐Phe‐L‐Val‐D‐Ala)].
- Published in:
- Journal of Heterocyclic Chemistry, 2022, v. 59, n. 1, p. 131, doi. 10.1002/jhet.4371
- By:
- Publication type:
- Article
Antimicrobial and antiproliferative study of chalcone clubbed 2,4‐dimethylpyrrole‐3‐carboxamide derivatives: Synthesis and in vitro evaluation.
- Published in:
- Journal of Heterocyclic Chemistry, 2022, v. 59, n. 1, p. 119, doi. 10.1002/jhet.4370
- By:
- Publication type:
- Article
A high‐yielding protocol for the synthesis of 4,5‐diarylpyrimidin‐2‐amine derivatives from chalcones.
- Published in:
- Journal of Heterocyclic Chemistry, 2022, v. 59, n. 1, p. 112, doi. 10.1002/jhet.4369
- By:
- Publication type:
- Article
Application of diazonium chemistry in purine modifications: A focused review.
- Published in:
- 2022
- By:
- Publication type:
- Literature Review
Convergent synthesis, drug target prediction, and docking studies of new 2,6,9‐trisubstituted purine derivatives.
- Published in:
- Journal of Heterocyclic Chemistry, 2022, v. 59, n. 1, p. 97, doi. 10.1002/jhet.4368
- By:
- Publication type:
- Article
Issue Information.
- Published in:
- Journal of Heterocyclic Chemistry, 2022, v. 59, n. 1, p. 1, doi. 10.1002/jhet.4289
- Publication type:
- Article
A convenient synthetic approach to a novel class of aryldifluoromethyl pyrimidine derivatives containing strobilurin motif as insecticidal agents.
- Published in:
- Journal of Heterocyclic Chemistry, 2022, v. 59, n. 1, p. 88, doi. 10.1002/jhet.4367
- By:
- Publication type:
- Article
Synthesis, biological evaluation, and molecular docking study of thiophene‐, piperazine‐, and thiazolidinone‐based hybrids as potential antimicrobial agents.
- Published in:
- Journal of Heterocyclic Chemistry, 2022, v. 59, n. 1, p. 75, doi. 10.1002/jhet.4366
- By:
- Publication type:
- Article