Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Garima Sumran"'
Publikováno v:
ARKIVOC, Vol 2019, Iss 6, Pp 190-199 (2019)
Externí odkaz:
https://doaj.org/article/f2fdf953c2b74bcba916c27189efcd72
Publikováno v:
ARKIVOC, Vol 2007, Iss 15, Pp 292-302 (2007)
Externí odkaz:
https://doaj.org/article/069a6686bc3948718556e0457fd00d0a
Publikováno v:
Letters in Organic Chemistry. 18:532-537
An expeditious and operationally simple reaction between 3-hydrazonobutan-2-one oxime and different substituted benzaldehydes in the presence of silica afforded an unexpected product, biacetyl bis-hydrazone Schiff bases in good yield on grinding in a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf642e44d9398fa38eb791a6b2250280
https://doi.org/10.2174/1570178617999200818210859
https://doi.org/10.2174/1570178617999200818210859
Publikováno v:
Topics in Current Chemistry (Cham)
The present review article strives to compile the latest synthetic approaches for the synthesis of triazolothiadiazine and its derivatives, along with their diverse pharmacological activities, viz. anticancer, antimicrobial, analgesic and anti-inflam
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07eb8c98d2f763845e794bc5a1f11725
https://doi.org/10.1007/s41061-022-00365-x
https://doi.org/10.1007/s41061-022-00365-x
Publikováno v:
ARKIVOC, Vol 2019, Iss 6, Pp 190-199 (2019)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aed07b98c122dd4196801388754d925d
https://doi.org/10.24820/ark.5550190.p011.009
https://doi.org/10.24820/ark.5550190.p011.009
Synthesis and structural studies of 3,6-disubstituted-bis-1,2,4-triazolo-[4,3-b][3′,4′-f]pyridazines
Publikováno v:
Journal of Molecular Structure. 1185:379-391
Synthesis of a series of 3,6-disubstituted-bis-1,2,4-triazolo-[4,3-b][3′,4′-f]pyridazines (4) was accomplished by the oxidative intramolecular cyclization of 6-arylidenehydrazino-3-aryl-1,2,4-triazolo[4,3-b]pyridazine (3) using iodobenzene diacet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::502be6e5d13d22a447edfb48233c4c1d
https://doi.org/10.1016/j.molstruc.2019.02.082
https://doi.org/10.1016/j.molstruc.2019.02.082
Autor:
Ranjana Aggarwal, Garima Sumran
Publikováno v:
European Journal of Medicinal Chemistry
The present review aims to summarize the pharmacological profile of 1,2,4-triazole, one of the emerging privileged scaffold, as antifungal, antibacterial, anticancer, anticonvulsant, antituberculosis, antiviral, antiparasitic, analgesic and anti-infl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3d5c0f6a0fbe82cc96194dbc0d0a5c6
http://europepmc.org/articles/PMC7384432
http://europepmc.org/articles/PMC7384432
Reaction of 3-hydrazonobutan-2-one oxime with aromatic aldehydes resulted in the formation of 1,2-bis(arylidene)hydrazine commonly referred as azine as an unexpected product, instead of expected product 3-(aryl)methylenehydrazonobutan-2-one oxime, wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77875d51587fcaeea8ef98166502b079
Autor:
Garima Sumran, Ranjana Aggarwal
Publikováno v:
Journal of Sulfur Chemistry. 36:170-177
Several 2-arylimidazo[2,1-b]benzothiazoles (4) have been conveniently synthesized in one-pot reactions via α-tosyloxylation of enolizable ketones (1) using [hydroxy(tosyloxy)iodo]benzene 2 in acetonitrile, followed by treatment with 2-amino-6-(subst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4bbb564a463e69b57d53c376d6bd3320
https://doi.org/10.1080/17415993.2014.996221
https://doi.org/10.1080/17415993.2014.996221
Publikováno v:
Synthetic Communications. 44:923-928
A series of 2-(arylimino)-3-(hydroxyimino)butanes 3a–g, easily accessed by the condensation of variously substituted anilines 1a–g with biacetyl monoxime 2, were efficiently cyclized to afford 2,3-dimethylquinoxaline-1-oxides 4a–g using bis(ace
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49c55f3ce2fc067efac414fb29a13bca
https://doi.org/10.1080/00397911.2013.832775
https://doi.org/10.1080/00397911.2013.832775