Microwave‐Assisted Green Synthesis of 2,3‐Dihydroquinazolinones under Base‐ and Catalyst‐Free conditions

[1]  Puttinan Meepowpan,et al.  Commercial Copper-Catalyzed Aerobic Oxidative Synthesis of Quinazolinones from 2-Aminobenzamide and Methanol , 2020 .

[2]  B. Akhlaghinia,et al.  An Efficient Green Protocol for Synthesis of 2,3‐Dihydroquinazolin‐4(1H)‐ones Using SBA‐16/GPTMS‐TSC‐CuIunder Solvent‐Free Conditions , 2020 .

[3]  P. Ghosh,et al.  Ascorbic Acid as an Efficient Organocatalyst for the Synthesis of 2‐Substituted‐2,3‐dihydroquinazolin‐4(1 H )‐one and 2‐Substituted Quinazolin‐4(3 H )‐one in Water , 2020, ChemistrySelect.

[4]  S. Arunkumar,et al.  Citrus Extract Modified Graphene Oxide as a Green and Heterogeneous Organocatalyst for the Synthesis of Imidazole Derivatives , 2020 .

[5]  Wei Yao,et al.  Iridium Supported on Phosphorus‐Doped Porous Organic Polymers: Active and Recyclable Catalyst for Acceptorless Dehydrogenation and Borrowing Hydrogen Reaction , 2019, Advanced Synthesis & Catalysis.

[6]  Weizhen Zeng,et al.  Merrifield resin-supported quinone as an efficient biomimetic catalyst for metal-free, base-free, chemoselective synthesis of 2,4,6-trisubstituted pyridines , 2019, Green Chemistry.

[7]  Yejun Qiu,et al.  Immobilization of manganese dioxide nanoparticles on modified poly 2,4-dichlorostyrene microspheres: a highly efficient and recyclable catalyst for borrowing hydrogen reactions , 2019, Organic Chemistry Frontiers.

[8]  Wanyi Liu,et al.  High acidity cellulose sulfuric acid from sulfur trioxide: a highly efficient catalyst for the one step synthesis of xanthene and dihydroquinazolinone derivatives , 2019, RSC advances.

[9]  A. Yadav,et al.  Green and efficient one-pot synthesis of 2,3-dihydroquinazolin-4(1H)-ones and their anthelmintic studies , 2019, Synthetic Communications.

[10]  R. Nagarajan,et al.  Deep eutectic solvent mediated synthesis of quinazolinones and dihydroquinazolinones: synthesis of natural products and drugs , 2016 .

[11]  Xiang-Xiong Li,et al.  Y(OTf) 3 -catalyzed heterocyclic formation via aerobic oxygenation: An approach to dihydro quinazolinones and quinazolinones , 2015 .

[12]  Tao-Li Deng,et al.  Highly enantioselective synthesis of dihydroquinazolinones through Sc(OTf)3-catalyzed intramolecular amidation of imines , 2015 .

[13]  A. Ogawa,et al.  Regioselective hydrothiolation of alkenes bearing heteroatoms with thiols catalyzed by palladium diacetate. , 2014, The Journal of organic chemistry.

[14]  H. Neumann,et al.  Cascade synthesis of quinazolinones from 2-aminobenzonitriles and aryl bromides via palladium-catalyzed carbonylation reaction , 2014 .

[15]  S. Santra,et al.  Metal nanoparticles in “on-water” organic synthesis: one-pot nano CuO catalyzed synthesis of isoindolo[2,1-a]quinazolines , 2013 .

[16]  M. Nishida,et al.  Total synthesis of schizocommunin and revision of its structure. , 2013, Journal of natural products.

[17]  Pravin V. Shinde,et al.  A facile and rapid access towards the synthesis of 2,3-dihydroquinazolin-4(1H)-ones , 2013 .

[18]  Tian-bin Li,et al.  A recyclable CuO-catalyzed synthesis of 4(3H)-quinazolinones , 2013 .

[19]  Hidemasa Hikawa,et al.  Pd-catalyzed benzylic C-H amidation with benzyl alcohols in water: a strategy to construct quinazolinones. , 2012, The Journal of organic chemistry.

[20]  V. Kesavan,et al.  Highly enantioselective synthesis of 2,3-dihydroquinazolinones through intramolecular amidation of imines. , 2012, Organic letters.

[21]  Deepty Sharma,et al.  Cyanuric chloride catalyzed mild protocol for synthesis of biologically active dihydro/spiro quinazolinones and quinazolinone-glycoconjugates. , 2012, The Journal of organic chemistry.

[22]  M. Abdollahi-Alibeik,et al.  Synthesis of 2,3-dihydroquinazolin-4(1H)-ones catalyzed by zirconium (IV) chloride as a mild and efficient catalyst , 2011 .

[23]  A. Vinu,et al.  Cellulose-SO3H: an efficient and biodegradable solid acid for the synthesis of quinazolin-4(1H)-ones , 2011 .

[24]  C. Oliver Kappe,et al.  A critical assessment of the greenness and energy efficiency of microwave-assisted organic synthesis , 2011 .

[25]  Tingting Zhang,et al.  Eco-friendly synthesis of 2-substituted-2,3-dihydro-4(1H)-quinazolinones in water , 2011 .

[26]  Ke-Fang Yang,et al.  Combinatorial synthesis of 3-arylideneaminoquinazolin-4(1H)-one derivatives catalyzed by iodine in ionic liquids. , 2011, ACS combinatorial science.

[27]  Zhan‐Hui Zhang,et al.  Synthesis of 2,3-dihydroquinazolin-4(1H)-ones by three-component coupling of isatoic anhydride, amines, and aldehydes catalyzed by magnetic Fe(3)O(4) nanoparticles in water. , 2010, Journal of combinatorial chemistry.

[28]  A. Fakhari,et al.  Highly efficient solvent-free synthesis of quinazolin-4(3H)-ones and 2,3-dihydroquinazolin-4(1H)-ones using tetrabutylammonium bromide as novel ionic liquid catalyst , 2010 .

[29]  H. Shaterian,et al.  Synthesis of 2,3-Dihydroquinazoline-4(1H)-ones , 2010 .

[30]  Qi Zhang,et al.  Facile and One-Pot Synthesis of 1,2-Dihydroquinazolin-4(3H)-ones via Tandem Intramolecular Pinner/Dimroth Rearrangement , 2010 .

[31]  Yuyang Jiang,et al.  A simple and efficient approach to quinazolinones under mild copper-catalyzed conditions. , 2009, Angewandte Chemie.

[32]  A. Maleki,et al.  Click Reaction: Highly Efficient Synthesis of 2,3-Dihydroquinazolin-4(1H)-ones , 2008 .

[33]  Zhen Li,et al.  A Novel Method for the Synthesis of 4(3H)-Quinazolinones , 2008 .

[34]  N. Shadjou,et al.  Synthesis of New 2-Aryl Substituted 2,3-Dihydroquinazoline-4(1H)-ones Under Solvent-Free Conditions, Using Molecular Iodine as a Mild and Efficient Catalyst , 2008 .

[35]  W. Su,et al.  Eco-friendly synthesis of 2,3 -dihydroquinazolin -4 (1H) -ones in ionic liquids or ionic liquid-water without additional catalyst , 2007 .

[36]  Y. Wang,et al.  A facile synthesis of 2-substituted-2,3-dihydro-4(1H)-quinazolinones in 2,2,2-trifluoroethanol , 2007 .

[37]  W. Su,et al.  A facile synthesis of 2,3-dihydro-2-aryl-4(1H)-quinazolinones catalyzed by scandium(III) triflate , 2007 .

[38]  M. Zolfigol,et al.  A Novel Method for the One-Pot Three-Component Synthesis of 2,3-Dihydroquinazolin-4(1H)-ones , 2005 .

[39]  Yuyang Jiang,et al.  Synthesis and in vitro antitumor activity of 4(3H)-quinazolinone derivatives with dithiocarbamate side chains. , 2005, Bioorganic & medicinal chemistry letters.

[40]  K. Nishimura,et al.  Isolation of a new potent cytotoxic pigment along with indigotin from the pathogenic basidiomycetous fungus Schizophyllum commune , 2004, Mycopathologia.

[41]  D. Shi,et al.  Synthesis of quinazolin-4(3H)-ones and 1,2-dihydroquinazolin-4(3H)-ones with the aid of a low-valent titanium reagent , 2003 .

[42]  P. Lu,et al.  A one‐pot synthesis of 2‐aryl‐2,3‐dihydro‐4(lH)‐quinazolinones by use of samarium iodide , 2002 .

[43]  B. Roth,et al.  Novel nonpeptide CCK-B antagonists: design and development of quinazolinone derivatives as potent, selective, and orally active CCK-B antagonists. , 1998, Journal of medicinal chemistry.

[44]  T. Saeki,et al.  Cyclic GMP phosphodiesterase inhibitors. 2. Requirement of 6-substitution of quinazoline derivatives for potent and selective inhibitory activity. , 1994, Journal of medicinal chemistry.

[45]  J. F. Wolfe,et al.  Synthesis and anticonvulsant activity of some new 2-substituted 3-aryl-4(3H)-quinazolinones. , 1990, Journal of medicinal chemistry.

[46]  Y. Yamada,et al.  Studies on 4(1H)-quinazolinones. 5. Synthesis and antiinflammatory activity of 4(1H)-quinazolinone derivatives. , 1985, Journal of medicinal chemistry.