Zobrazeno 1 - 10
of 32
pro vyhledávání: '"G. L. Talesara"'
Publikováno v:
E-Journal of Chemistry, Vol 4, Iss 2, Pp 166-172 (2007)
Mebendazole is a well known anti-helimintic and belongs to the benzimidazole group of medicines. In order to achieve better medicinal results, i.e. enhanced activity and low toxicity, structural modifications are made in the existing drugs. Some 5-be
Externí odkaz:
https://doaj.org/article/07201c291c7c46f5b6b8c4f61ee36a88
Publikováno v:
E-Journal of Chemistry, Vol 3, Iss 1, Pp 28-34 (2006)
3-Methylpyrazol-5-one 3 reacts with substituted benzaldehydes 4a-d in the presence of anhydrous sodium acetate to produce the corresponding 4-arylidene-5-methyl-2,4-dihydro-pyrazol-3-ones 5a-d and the condensation of 5a-d with 2-bromoalkoxy-1H-isoind
Externí odkaz:
https://doaj.org/article/bad2fef574144020b4bf256b4fbe23b0
Publikováno v:
SKIT Research Journal. 12:86-94
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::474f6e856d6da37d5777db6ae1f7fb9d
https://doi.org/10.47904/ijskit.12.1.2022.86-94
https://doi.org/10.47904/ijskit.12.1.2022.86-94
Autor:
Maqbool Ahmed, Ajit Joshi, Prabhunath Yogi, Prakash Prajapat, Saba Khan, Mohammed Ashid, Nasir Hussain, G. L. Talesara
Publikováno v:
Journal of Heterocyclic Chemistry. 54:993-998
A one-pot three components synthesis of substituted bis[1-N,7-N-diethoxyphthalimido-4,4′-{3,5-dimethyl-4-(4-N,N-dimethylaminophenyl)-4,7-dihydro-1H-dipyrazolo[3,4-b;4′,3′-e] pyridin-8-yl}-phenyl] in moderate to high yields has been achieved by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aba39669d917e1104bc648466daede22
https://doi.org/10.1002/jhet.2665
https://doi.org/10.1002/jhet.2665
Publikováno v:
Indian Journal of Pharmaceutical Sciences
Thiazolidin-4-one fused pyrimidines, [1,5]-benzodiazepines and their oxygen substituted hydroxylamine derivatives have been screened for antibacterial, antifungal and antimalarial activity. Bacillus subtilis, Escherichia coli, Proteus mirabilis and S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a130bf77a8af0fc0299957f8805aef0
http://europepmc.org/articles/PMC3116306
http://europepmc.org/articles/PMC3116306
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry. 23:882-887
A facile synthesis of 5,5'-(1,4-phenylene)bis(3-aryl-2-pyrazolines) 4a-g has been achieved by the cyclo-addition reaction of hydrazine hydrate with bis-substituted chalcones 3a-g, which in turn were prepared by the Clasien-Schmidt condensation of p-s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7aff4edbbe315afa4b8b087dbea8c8e4
https://doi.org/10.1080/14756360701442332
https://doi.org/10.1080/14756360701442332
Publikováno v:
E-Journal of Chemistry, Vol 4, Iss 2, Pp 166-172 (2007)
Mebendazole is a well known anti-helimintic and belongs to the benzimidazole group of medicines. In order to achieve better medicinal results, i.e. enhanced activity and low toxicity, structural modifications are made in the existing drugs. Some 5-be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef545d1139e97edba09d07d65a83878c
https://doaj.org/article/07201c291c7c46f5b6b8c4f61ee36a88
https://doaj.org/article/07201c291c7c46f5b6b8c4f61ee36a88
Publikováno v:
Journal of Sulfur Chemistry. 27:445-453
1,3-Thiazolidine-2,4-dione 2 has been synthesized by the cyclisation reaction of thiourea and chloroacetic acid in the presence of ethanol. The reaction of compound 2 with substituted aromatic aldehyde afforded the corresponding derivatives of substi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6590d1cbb5b7f58594b9ef7eab6c7270
https://doi.org/10.1080/17415990600904697
https://doi.org/10.1080/17415990600904697
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 181:1665-1673
Some novel azaimidoxy compounds viz. 2-{[(4-chlorophenyl)diazenyl]oxy}-1H-isoindole-1,3-(2H)-dione (Va), and 1-{[1-naphthyldiazenyl]oxy}pyrrolidine-2,5-dione (IVc), etc. have been synthesized by a simple diazotization reaction followed by a coupling
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9d9ec3498d6816ff610ff2e8ec89e012
https://doi.org/10.1080/10426500500366970
https://doi.org/10.1080/10426500500366970
Publikováno v:
Scopus-Elsevier
ARKIVOC, Vol 2006, Iss 11, Pp 66-75 (2006)
ARKIVOC, Vol 2006, Iss 11, Pp 66-75 (2006)
Hydroxyquinoline 1 reacts with ethyl chloroacetate in the presence of anhydrous K2CO3 to produce ethyl (quinolin-8-yloxy)acetate 2. Treatment of 2 with hydrazine hydrate forms 2- (quinolin-8-yloxy)acetohydrazide 3, which on condensation with various
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b45cf233eb9cd004a01aefcef195248
https://doi.org/10.3998/ark.5550190.0007.b06
https://doi.org/10.3998/ark.5550190.0007.b06