380639-22-5Relevant articles and documents
Dihydropyrimidones: As novel class of β-glucuronidase inhibitors
Ali, Farman,Khan, Khalid Mohammed,Salar, Uzma,Iqbal, Sarosh,Taha, Muhammad,Ismail, Nor Hadiani,Perveen, Shahnaz,Wadood, Abdul,Ghufran, Mehreen,Ali, Basharat
, p. 3624 - 3635 (2016/07/21)
Dihydropyrimidones 1–37 were synthesized via a ‘one-pot’ three component reaction according to well-known Biginelli reaction by utilizing Cu(NO3)2·3H2O as catalyst, and screened for their in vitro β-glucuronidase inhibitor
Zn2+/MCM-41 catalyzed Biginelli reaction of heteroaryl aldehydes and evaluation of the antimicrobial activity and cytotoxicity of the pyrimidone products
Ghasemi, Zarrin,Farshbaf Orafa, Farzaneh,Pirouzmand, Mahtab,Zarrini, Gholamreza,Nikzad Kojanag, Behnaz,Salehi, Roya
supporting information, p. 6393 - 6396 (2015/11/16)
The three component Biginelli condensation of various aryl aldehydes, 1,3-dicarbonyls and urea was investigated in the presence of free or MCM-41 supported ZnNO3. The pyrimidone products, which were obtained under solvent-free conditions, were