Bi (TFA) 3-[nbp] Fecl4: A new, efficient and reusable promoter system for the synthesis of 4(3H)-quinazolinone derivatives
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Studies on some biologically active substituted 4(3H)-quinazolinones. Part 1.Synthesis, characterization and anti-inflammatory, antimicrobial activity of 6,8-disubstituted 2-phenyl-3-[substituted- Benzothiazol- 2-yl]-4(3H)-quinazolinone
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Synthesis and in vitro antitumor activity of 4(3H)-quinazolinone derivatives with dithiocarbamate side chains
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Studies on quinazolinones as dual inhibitors of Pgp and MRP1 in multidrug resistance
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A one- Pot synthesis of novel sugar derived 5,6- dihydro-quinazolino [4,3-b] quinazolin-8-one:an entry towards highly fuctionalized sugarheterocyclic hybrids
Deb roy A, Subramanian A, Mukhopadhyay B, Roy R. A one- pot synthesis of novel sugar derived 5,6- dihydro-quinazolino [4,3-b] quinazolin-8-one :an entry towards highly fuctionalized sugarheterocyclic hybrids. Tetrahedron Lett. 2006;47: 6857-6860.
Hexamethyldisilazane-iodine induced intramolecular dehydrative cyclization of diamides: A general access to natural and unnatural quinazolinones
DOI 10.1016/j.tetlet.2007.03.032, PII S0040403907004698
Kshirsagar UA, Mhaske SB, Argade NP. Hexamethyldisilazane-iodine induced intramolecular dehydrative cyclization of diamides: a general access to natural and unnatural quinazolinones. Tetrahedron Lett. 2007;48:3243-3246. (Pubitemid 46527755)
Recent progress in the synthesis of heterocyclic natural products by the Staudinger/ intramolecular aza-witting reaction
Eguchi S. Recent progress in the synthesis of heterocyclic natural products by the Staudinger/ intramolecular aza-witting reaction. Arkivoc. 2005.p .98-119.
Synthesis and biological evaluation of some new 2-propyl-4(3H)- quinazolinone derivatives as anti-bacterial
Eissa AMF, El-metwally AM, El-hashash MA, Elgohary AMF. Synthesis and biological evaluation of some new 2-propyl-4(3H)-quinazolinone derivatives as anti-bacterial. J korean chem Soc. 2008;52:328-337.