Works matching IS 0022152X AND DT 2022 AND VI 59 AND IP 7
Results: 16
Synthesis and antimicrobial evaluation of novel tris‐thiadiazole derivatives.
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- Journal of Heterocyclic Chemistry, 2022, v. 59, n. 7, p. 1253, doi. 10.1002/jhet.4466
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Simple grinding for the synthesis of monomeric, dimeric, and trimeric pyridinium salts and its photophysical studies.
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- Journal of Heterocyclic Chemistry, 2022, v. 59, n. 7, p. 1260, doi. 10.1002/jhet.4467
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Direct C‐2 arylation of quinoxaline with arylhydrazine salts as arylation reagents.
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- Journal of Heterocyclic Chemistry, 2022, v. 59, n. 7, p. 1272, doi. 10.1002/jhet.4465
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Synthesis and herbicidal activities of 2‐phenylpyridine compounds containing alkenyl moieties.
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- Journal of Heterocyclic Chemistry, 2022, v. 59, n. 7, p. 1247, doi. 10.1002/jhet.4464
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Synthesis a group of 5(6)‐substituted benzimidazole Zn(II) and Co(II) complexes and investigation their cytotoxic and antimicrobial activities.
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- Journal of Heterocyclic Chemistry, 2022, v. 59, n. 7, p. 1241, doi. 10.1002/jhet.4463
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Synthesis, characterization and crystal structure of some novel partially hydrogenated isoquinolines and their fused heterocyclic systems.
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- Journal of Heterocyclic Chemistry, 2022, v. 59, n. 7, p. 1230, doi. 10.1002/jhet.4462
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One‐step synthesis of novel N1‐substituted benzimidazole derivatives: Experimental and theoretical investigations.
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- Journal of Heterocyclic Chemistry, 2022, v. 59, n. 7, p. 1213, doi. 10.1002/jhet.4461
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Synthesis and biological evaluation of novel 2‐arylquinoline‐3‐fused thiazolo[2,3‐c]1,2,4‐triazole heterocycles as potential antiproliferative and antimicrobial agents.
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- Journal of Heterocyclic Chemistry, 2022, v. 59, n. 7, p. 1198, doi. 10.1002/jhet.4460
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Efficient synthesis of benzo[h]carbazol[3,2‐b][1,6]naphthyridines.
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- Journal of Heterocyclic Chemistry, 2022, v. 59, n. 7, p. 1191, doi. 10.1002/jhet.4459
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Microwave assisted synthesis of N‐substituted acridine‐1,8‐dione derivatives: Evaluation of antimicrobial activity.
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- Journal of Heterocyclic Chemistry, 2022, v. 59, n. 7, p. 1180, doi. 10.1002/jhet.4458
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An investigation of chiral diamides as organocatalysts in asymmetric aldol reaction.
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- Journal of Heterocyclic Chemistry, 2022, v. 59, n. 7, p. 1169, doi. 10.1002/jhet.4457
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p‐Toluenesulfonic acid catalyzed, isocyanide‐free, Groebke–Blackburn–Bienayme (GBB) type multicomponent synthesis of 3‐anilino‐imdazo[1,2‐a]pyridines.
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- Journal of Heterocyclic Chemistry, 2022, v. 59, n. 7, p. 1266, doi. 10.1002/jhet.4456
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Design and synthesis novel amide derivatives containing an 1,3,4‐oxadiazole moiety as potential antibacterial agents.
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- Journal of Heterocyclic Chemistry, 2022, v. 59, n. 7, p. 1160, doi. 10.1002/jhet.4455
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Novel N‐substituted isatin‐ampyrone Schiff bases as a new class of antiproliferative agents: Design, synthesis, molecular modeling and in vitro cytotoxic activity.
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- Journal of Heterocyclic Chemistry, 2022, v. 59, n. 7, p. 1144, doi. 10.1002/jhet.4454
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Recent advances in the synthetic method and mechanism for the important N‐heterocyclic compound of 3‐methylindole.
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- Journal of Heterocyclic Chemistry, 2022, v. 59, n. 7, p. 1135, doi. 10.1002/jhet.4451
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Issue Information.
- Published in:
- Journal of Heterocyclic Chemistry, 2022, v. 59, n. 7, p. 1131, doi. 10.1002/jhet.4295
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- Article