Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Fatemeh Madani Qamsari"'
Autor:
Fatemeh Madani Qamsari, Shahram Moradi, Alireza Foroumadi, Mohammad Mahdavi, Abolghasem Moghimi
Publikováno v:
Iranian Journal of Chemistry & Chemical Engineering, Vol 40, Iss 2, Pp 437-443 (2021)
An eco-friendly, highly efficient, and tandem reaction between 2-hydroxy-1,4-naphthoquinone and quinolinium salts in the presence of DABCO, 1,4-diazabicyclo[2.2.2]octane, in an aqueous medium is developed for the synthesis of functionalized polycycli
Externí odkaz:
https://doaj.org/article/b15924655de242768cadc618c75ad480
Autor:
Shahram Moradi, Fatemeh Madani Qamsari, Abolghasem Moghimi, Mohammad Mahdavi, Alireza Foroumadi
Publikováno v:
Monatshefte für Chemie - Chemical Monthly. 150:347-352
An efficient and facile method for the synthesis of novel naphthooxazocines from 2-hydroxy-1,4-naphthoquinone and quinolinium salts at room temperature is described. The reaction proceeds through C-alkylation and intramolecular O-alkylation, affordin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec8798d51b61b1bf43ef340f463cdb37
https://doi.org/10.1007/s00706-018-2322-8
https://doi.org/10.1007/s00706-018-2322-8
Autor:
Loghman Firoozpour, Fatemeh Madani-Qamsari, Roya Pakrad, Somayeh Mojtabavi, Somayeh Salarinejad, Mohammad Ali Faramarzi, Mahsa Toolabi, Saeed Karima, Fatemeh Safari, Setareh Moghimi, Seyed Esmaeil Sadat Ebrahimi, Alireza Foroumadi
Publikováno v:
Bioorganic Chemistry. 109:104670
In this study, we reported the discovery of pyridazine based 1,2,3-triazole derivatives as inhibitors of α-glucosidase. All target compounds exhibited significant inhibitory activities against yeast and rat α-glucosidase enzymes compared to positiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4fa140fa0cc1e008bbbce2d99faae179
https://doi.org/10.1016/j.bioorg.2021.104670
https://doi.org/10.1016/j.bioorg.2021.104670