Bismuth-Catalyzed Synthesis of 2-Substituted Quinazolinones.

[1]  Yi Pan,et al.  Metal-free oxidative cyclization of 2-amino-benzamides, 2-aminobenzenesulfonamide or 2-(aminomethyl)anilines with primary alcohols for the synthesis of quinazolinones and their analogues , 2018 .

[2]  Ge-xin Chen,et al.  Direct synthesis of quinazolinones by heterogeneous Cu(OH)X/OMS-2 catalyst under oxygen , 2018 .

[3]  Sandeep Kumar,et al.  Zirconia Supported Cu (I) Stabilized Copper Oxide Mesoporous Catalyst for the Synthesis of Quinazolinones Under Ambient Conditions , 2017 .

[4]  S. Sinha,et al.  One-Pot Cascade Synthesis of Quinazolin-4(3H)-ones via Nickel-Catalyzed Dehydrogenative Coupling of o-Aminobenzamides with Alcohols. , 2017, The Journal of organic chemistry.

[5]  T. Xiao,et al.  Iridium‐Catalyzed Cyclization of o‐Aminobenzamides with Unsaturated Aldehydes to Give 2‐Alkylquinazolinones through a Hydrogen Autotransfer Process , 2017 .

[6]  J. Niu,et al.  A facile vanadium-catalyzed aerobic oxidative synthesis of quinazolinones from 2-aminobenzamides with aldehydes or alcohols , 2016 .

[7]  Dinesh Kumar,et al.  Indium-Mediated Stereoselective Allylation. , 2016, Accounts of chemical research.

[8]  G. R. Cook,et al.  Palladium-Catalyzed Allylic Amidation with N-Heterocycles via sp3 C–H Oxidation , 2016 .

[9]  Dinesh Kumar,et al.  Merging C–H Bond Functionalization with Amide Alcoholysis: En Route to 2-Aminopyridines , 2016 .

[10]  P. Liu,et al.  Quinazolinones from o‐Aminobenzonitriles by One‐Pot Sequential Selective Hydration/Condensation/Acceptorless Dehydrogenation Catalyzed by an Iridium Complex , 2016 .

[11]  L. Tang,et al.  Heterogeneous Gold-Catalyzed Cascade Hydrogen-Transfer Strategy for Selective Synthesis of Quinazolinones in Water , 2016 .

[12]  Asish R. Das,et al.  Synthesis of 2,3-dihydroquinazolinones and quinazolin-4(3H)-ones catalyzed by graphene oxide nanosheets in an aqueous medium: “on-water” synthesis accompanied by carbocatalysis and selective C–C bond cleavage , 2016 .

[13]  Xiong Zhengxin,et al.  Copper-catalyzed consecutive reaction to construct quinazolin-4(3H)-ones and pyrido[2,3-d]pyrimidin-4(3H)-ones , 2016 .

[14]  Xiao‐Feng Wu,et al.  Synthesis of quinazolinones from o-aminobenzamides and benzyl amines under metal-free conditions , 2016 .

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

[16]  Shengzheng Wang,et al.  Scaffold Diversity Inspired by the Natural Product Evodiamine: Discovery of Highly Potent and Multitargeting Antitumor Agents. , 2015, Journal of medicinal chemistry.

[17]  Dinesh Kumar,et al.  Highly chemo- and regioselective allylic substitution with tautomerizable heteroarenes , 2015 .

[18]  S. Bharate,et al.  Iodine Catalyzed Oxidative Synthesis of Quinazolin-4(3H)-ones and Pyrazolo[4,3-d]pyrimidin-7(6H)-ones via Amination of sp(3) C-H Bond. , 2015, The Journal of organic chemistry.

[19]  Dinesh Kumar,et al.  N-Boc-glycine-assisted indium-mediated allylation reaction: a sustainable approach , 2015 .

[20]  Jianmin Lu,et al.  The cascade synthesis of quinazolinones and quinazolines using an α-MnO2 catalyst and tert-butyl hydroperoxide (TBHP) as an oxidant. , 2015, Chemical communications.

[21]  Dinesh Kumar,et al.  Convenient synthesis of 2,3-disubstituted quinazolin-4(3H)-ones and 2-styryl-3-substituted quinazolin-4(3H)-ones: applications towards the synthesis of drugs , 2015 .

[22]  M. Suckow,et al.  Discovery of antibiotic (E)-3-(3-carboxyphenyl)-2-(4-cyanostyryl)quinazolin-4(3H)-one. , 2015, Journal of the American Chemical Society.

[23]  Yangmin Ma,et al.  CuO nanoparticles catalyzed simple and efficient synthesis of 2,3-dihydroquinazolin-4(1H)-ones and quinazolin-4(3H)-ones under ultrasound irradiation in aqueous ethanol under ultrasound irradiation in aqueous ethanol , 2014 .

[24]  S. Yin,et al.  Metal-free aerobic oxidative C-N bond cleavage of tertiary amines for the synthesis of N-heterocycles with high atom efficiency. , 2014, Organic & biomolecular chemistry.

[25]  S. Ji,et al.  Palladium-catalyzed one-pot synthesis of quinazolinones via tert-butyl isocyanide insertion. , 2014, The Journal of organic chemistry.

[26]  S. H. Siddiki,et al.  Direct synthesis of quinazolinones by acceptorless dehydrogenative coupling of o-aminobenzamide and alcohols by heterogeneous Pt catalysts , 2014 .

[27]  Yalin Tang,et al.  Copper‐Catalyzed Domino Reaction Involving C–C Bond Cleavage To Construct 2‐Aryl Quinazolinones , 2014 .

[28]  C. Cheon,et al.  Synthesis of quinazolinones from anthranilamides and aldehydes via metal-free aerobic oxidation in DMSO , 2014 .

[29]  R. Akula,et al.  An Efficient Synthesis of 2-Substituted Quinazolin-4(3H)-ones Catalyzed by Iron(III) Chloride , 2014 .

[30]  Jian-Xin Li,et al.  Iron-catalyzed oxidative synthesis of N-heterocycles from primary alcohols , 2014 .

[31]  Qin Yang,et al.  Cross-coupling/annulations of quinazolones with alkynes for access to fused polycyclic heteroarenes under mild conditions. , 2014, Organic & biomolecular chemistry.

[32]  R. Hayashi,et al.  Bi(OTf)3 as a Dual Role Catalyst. Synthesis of Substituted Morpholine Derivatives via Catalytic O-Allylation , 2014 .

[33]  M. D. Lloyd,et al.  Design and Discovery of 2-Arylquinazolin-4-ones as Potent and Selective Inhibitors of Tankyrases. , 2013, ACS medicinal chemistry letters.

[34]  H. Neumann,et al.  Palladium-catalyzed carbonylative synthesis of quinazolinones from 2-aminobenzamide and aryl bromides. , 2013, Chemistry.

[35]  R. Cheng,et al.  One-Pot Synthesis of Quinazolinones from Anthranilamides and Aldehydes via p-Toluenesulfonic Acid Catalyzed Cyclocondensation and Phenyliodine Diacetate Mediated Oxidative Dehydrogenation , 2013 .

[36]  Rajashri S. Salunkhe,et al.  Cp2ZrCl2-catalyzed synthesis of 2-substituted quinozolin-4(3H)-ones , 2013 .

[37]  Frank Glorius,et al.  C-H bond activation enables the rapid construction and late-stage diversification of functional molecules. , 2013, Nature chemistry.

[38]  Thierry Ollevier.  New trends in bismuth-catalyzed synthetic transformations. , 2013, Organic & biomolecular chemistry.

[39]  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.

[40]  A. Watson,et al.  Ruthenium-catalysed oxidative synthesis of heterocycles from alcohols. , 2012, Organic & biomolecular chemistry.

[41]  Jianguang Zhou,et al.  One-pot synthesis of quinazolinones via iridium-catalyzed hydrogen transfers. , 2011, The Journal of organic chemistry.

[42]  W. Xu,et al.  Amino acids as the nitrogen-containing motifs in copper-catalyzed domino synthesis of N-heterocycles. , 2011, The Journal of organic chemistry.

[43]  Hongxia Liu,et al.  Copper-catalyzed domino synthesis of quinazolinones via Ullmann-type coupling and aerobic oxidative C-H amidation. , 2011, Organic letters.

[44]  R. Mohan,et al.  Applications of bismuth(III) compounds in organic synthesis. , 2003, Chemical Society reviews.

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

[46]  Yuyang Jiang,et al.  Highly efficient copper-catalyzed cascade synthesis of quinazoline and quinazolinone derivatives. , 2008, Chemical communications.

[47]  R. Hayashi,et al.  Bi(OTf)(3)-Catalyzed 5-Exo-Trig Cyclization via Halide Activation. , 2008, Tetrahedron Letters.

[48]  W. Su,et al.  Gallium(III) triflate-catalyzed one-pot selective synthesis of 2,3-dihydroquinazolin-4(1H)-ones and quinazolin-4(3H)-ones , 2008 .

[49]  Martyn Poliakoff,et al.  Sustainable technology: Green chemistry , 2007, Nature.

[50]  R. Hayashi,et al.  Intermolecular Friedel–Crafts reaction catalyzed by InCl3 , 2007 .

[51]  Christian Capello,et al.  What is a green solvent? A comprehensive framework for the environmental assessment of solvents , 2007 .

[52]  R. Hayashi,et al.  Remarkably mild and efficient intramolecular Friedel-Crafts cyclization catalyzed by In(III). , 2007, Organic letters.

[53]  N. Argade,et al.  The Chemistry of Recently Isolated Naturally Occurring Quinazolinone Alkaloids , 2006 .

[54]  S. Hecht,et al.  Luotonin A. A naturally occurring human DNA topoisomerase I poison. , 2003, Journal of the American Chemical Society.

[55]  S Diamond,et al.  Inhibition of clinically relevant mutant variants of HIV-1 by quinazolinone non-nucleoside reverse transcriptase inhibitors. , 2000, Journal of medicinal chemistry.

[56]  Pietro Tundo,et al.  Synthetic pathways and processes in green chemistry. Introductory overview , 2000 .

[57]  Y. Wataya,et al.  New type of febrifugine analogues, bearing a quinolizidine moiety, show potent antimalarial activity against Plasmodium malaria parasite. , 1999, Journal of medicinal chemistry.

[58]  N. Liverton,et al.  Nonpeptide glycoprotein IIb/IIIa inhibitors: substituted quinazolinediones and quinazolinones as potent fibrinogen receptor antagonists. , 1998, Bioorganic & medicinal chemistry letters.

[59]  M. Malamas,et al.  Quinazolineacetic acids and related analogues as aldose reductase inhibitors. , 1991, Journal of medicinal chemistry.

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

[61]  N. Peet,et al.  3-(1H-tetrazol-5-yl)-4(3H)-quinazolinone sodium salt (MDL 427): a new antiallergic agent. , 1986, Journal of medicinal chemistry.