Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Esraa M. Osman"'
Autor:
Sara M. Mostafa, Ashraf A. Aly, Alaa A. Hassan, Esraa M. Osman, Stefan Bräse, Martin Nieger, Mahmoud A. A. Ibrahim, Asmaa H. Mohamed
Publikováno v:
Molecules, Vol 27, Iss 7, p 2125 (2022)
An efficient synthesis of a series of pyridazino[4,3-c:5,6-c′]diquinolines was achieved via the autoxidation of 4-hydrazinylquinolin-2(1H)-ones. IR, NMR (1H and 13C), mass spectral data, and elemental analysis were used to fit and elucidate the str
Externí odkaz:
https://doaj.org/article/9fefde9fba6541a78eacd141e7cfde3c
Autor:
Asmaa H. Mohamed, Sara M. Mostafa, Ashraf A. Aly, Alaa A. Hassan, Esraa M. Osman, AbdElAziz A. Nayl, Alan B. Brown, Elshimaa M. N. Abdelhafez
Publikováno v:
RSC Advances. 13:14631-14640
In an attempt to develop effective and safe antibacterial agents, thiazinanones bearing the quinolone scaffold were prepared by reaction of the corresponding (quinolinylmethylene)hydrazinecarbothioamides with 2,3-diphenylcycloprop-2-enone.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4fb96c5d7111ee97016a33664a00fcbc
https://doi.org/10.1039/d3ra01721d
https://doi.org/10.1039/d3ra01721d
Autor:
Ashraf A. Aly, Alaa A. Hassan, Sara M. Mostafa, Asmaa. H. Mohamed, Esraa M. Osman, AbdElAziz A. Nayl
Publikováno v:
RSC advances. 12(29)
Great attention has been paid to cyclopropenones as they are present in many natural sources. Various synthesized cyclopropenone derivatives also show a wide range of biological activities. The cyclopropenone derivatives undergo a variety of reaction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21833e8032a6da03a7d770d7a14c146a
https://pubmed.ncbi.nlm.nih.gov/35873324
https://pubmed.ncbi.nlm.nih.gov/35873324
Autor:
Mohamed, Sara M. Mostafa, Ashraf A. Aly, Alaa A. Hassan, Esraa M. Osman, Stefan Bräse, Martin Nieger, Mahmoud A. A. Ibrahim, Asmaa H.
Publikováno v:
Molecules; Volume 27; Issue 7; Pages: 2125
An efficient synthesis of a series of pyridazino[4,3-c:5,6-c′]diquinolines was achieved via the autoxidation of 4-hydrazinylquinolin-2(1H)-ones. IR, NMR (1H and 13C), mass spectral data, and elemental analysis were used to fit and elucidate the str
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::07be9a5f1d1d388f443496e03ebf83ee
Autor:
Martin Nieger, Asmaa H. Mohamed, Stefan Bräse, Esraa M. Osman, S.M. Mostafa, Mahmoud A. A. Ibrahim, Alaa A. Hassan, Ashraf A. Aly
Publikováno v:
Molecular Diversity
During formylation of 2-quinolones by DMF/Et3N mixture, the unexpected 3,3′-methylenebis(4-hydroxyquinolin-2(1H)-ones) were formed. The discussed mechanism was proved as due to the formation of 4-formyl-2-quinolone as intermediate. Reaction of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90fc675cec5e1a174c880c800f86a355
https://doi.org/10.1007/s11030-020-10140-z
https://doi.org/10.1007/s11030-020-10140-z