One-pot, Simple, and Convenient Synthesis of 2-Thioxo-2,3-dihydroquinazolin-4(1H)-ones
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[1] B. B. Mishra,et al. One-Pot Convenient and High Yielding Synthesis of Dithiocarbamates , 2007 .
[2] V. Alagarsamy,et al. Synthesis and pharmacological evaluation of some 3-phenyl-2-substituted-3H-quinazolin-4-one as analgesic, anti-inflammatory agents. , 2007, Bioorganic & medicinal chemistry.
[3] A. Subramanian,et al. Auto-redox reaction: tin(II) chloride-mediated one-step reductive cyclization leading to the synthesis of novel biheterocyclic 5,6-dihydro-quinazolino[4,3-b]quinazolin-8-ones with three-point diversity. , 2006, The Journal of organic chemistry.
[4] A. Katritzky,et al. Novel synthesis of bicycles with fused pyrrole, indole, oxazole, and imidazole rings. , 2004, The Journal of organic chemistry.
[5] T. Tsuji,et al. Solid-phase Synthesis of Quinazoline-2,4-diones Using SNAr Reaction , 2001 .
[6] S. Kuo,et al. 6-Alkylamino- and 2,3-dihydro-3'-methoxy-2-phenyl-4-quinazolinones and related compounds: their synthesis, cytotoxicity, and inhibition of tubulin polymerization. , 2000, Journal of medicinal chemistry.
[7] R. Lakhan,et al. Syntheses of Some New 4(3H)‐Quinazolinones as Potential CNS Active Agents , 1985, Archiv der Pharmazie.