Simple synthesis, binds and inhibits tubulin, and potent broad-spectrum cytotoxicity.
The fabricated catalyst Fe3O4@EDTA/CuI facilitates the synthesis of 2,3-dihydroquinazolin-4(1H)-ones under sustainable conditions with ideal values of green metrics in a short reaction time.
2,3-Dihydroquinazolin-4(1H)-one and tetrazole are a class of nitrogen-containing heterocyclic compounds that play an important role in drug design and are an important part of many biological and industrial compounds.
This study explores a novel and eco-friendly synthesis of 22 derivatives of 2-aryl/heteroaryl substituted 2,3-dihydroquinazolin-4(1H)-ones using concentrated solar radiation (CSR) and lemon juice as a natural catalyst.
In this study, an environmentally friendly and highly efficient one-pot procedure was introduced for the synthesis of pyrano[2,3-d]pyrimidinones via a three-component reaction featuring malononitrile, aldehydes, and barbituric acid.