Commercial Copper-Catalyzed Aerobic Oxidative Synthesis of Quinazolinones from 2-Aminobenzamide and Methanol

[1]  Haiyan Zhu,et al.  A Zirconium Indazole Carboxylate Coordination Polymer as an Efficient Catalyst for Dehydrogenation‐Cyclization and Oxidative Coupling Reactions , 2020 .

[2]  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.

[3]  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.

[4]  Haiyan Zhu,et al.  Unsymmetrical triazolyl-naphthyridinyl-pyridine bridged highly active copper complexes supported on reduced graphene oxide and their application in water , 2019, Green Chemistry.

[5]  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.

[6]  C. Duanmu,et al.  Copper-catalyzed tandem oxidative synthesis of quinazolinones from 2-aminobenzonitriles and benzyl alcohols , 2019, Organic Chemistry Frontiers.

[7]  G. Satish,et al.  Copper-catalyzed oxidative amination of methanol to access quinazolines. , 2019, Organic & biomolecular chemistry.

[8]  Liang‐Hua Zou,et al.  Thienylbenzotriazole promoted highly active gold nanoparticles supported on N-doped graphene as efficient catalysts in water and a mechanism exploration , 2019, Organic Chemistry Frontiers.

[9]  Qiang Wu,et al.  Preparation of pyridyltriazole ruthenium complexes as effective catalysts for the selective alkylation and one-pot C–H hydroxylation of 2-oxindole with alcohols and mechanism exploration , 2018 .

[10]  Xinxin Sang,et al.  BINAP-copper supported by hydrotalcite as an efficient catalyst for the borrowing hydrogen reaction and dehydrogenation cyclization under water or solvent-free conditions , 2018 .

[11]  Wei Yao,et al.  Unsymmetrical indazolyl-pyridinyl-triazole ligand-promoted highly active iridium complexes supported on hydrotalcite and its catalytic application in water , 2018 .

[12]  Duo-Sheng Wang,et al.  Tunable Triazole-Phosphine-Copper Catalysts for the Synthesis of 2-Aryl-1H-benzo[d]imidazoles from Benzyl Alcohols and Diamines by Acceptorless Dehydrogenation and Borrowing Hydrogen Reactions , 2017 .

[13]  M. Beller,et al.  Übergangsmetallkatalysierte Nutzung von Methanol als C1‐Quelle in der organischen Synthese , 2017 .

[14]  H. Neumann,et al.  Transition-Metal-Catalyzed Utilization of Methanol as a C1  Source in Organic Synthesis. , 2017, Angewandte Chemie.

[15]  N. Huang,et al.  Disulfide-Directed C–H Hydroxylation for Synthesis of Sulfonyl Diphenyl Sulfides and 2-(Phenylthio)phenols with Oxygen as Oxidant , 2017 .

[16]  N. Huang,et al.  Catalytic aza-Wittig Reaction of Acid Anhydride for the Synthesis of 4H-Benzo[d][1,3]oxazin-4-ones and 4-Benzylidene-2-aryloxazol-5(4H)-ones , 2016 .

[17]  Lei Lu,et al.  Acceptorless Dehydrogenative Coupling of o-Aminobenzamides with the Activation of Methanol as a C1 Source for the Construction of Quinazolinones. , 2016, Organic letters.

[18]  Soon Hyeok Hong,et al.  Ruthenium-Catalyzed Urea Synthesis Using Methanol as the C1 Source. , 2016, Organic letters.

[19]  U. A. Kshirsagar,et al.  Recent developments in the chemistry of quinazolinone alkaloids. , 2015, Organic & biomolecular chemistry.

[20]  A. Seayad,et al.  Efficient Ruthenium-Catalyzed N-Methylation of Amines Using Methanol , 2015 .

[21]  Soon Hyeok Hong,et al.  Hydrogen Acceptor‐ and Base‐Free N‐Formylation of Nitriles and Amines using Methanol as C1 Source , 2015 .

[22]  P. Andersson,et al.  C-C coupling of ketones with methanol catalyzed by a N-heterocyclic carbene-phosphine iridium complex. , 2015, Chemistry.

[23]  Yuqiang Ding,et al.  Synthesis, Structures of Benzoxazolyl Iridium(III) Complexes, and Applications on C–C and C–N Bond Formation Reactions under Solvent-Free Conditions: Catalytic Activity Enhanced by Noncoordinating Anion without Silver Effect , 2014 .

[24]  Y. Obora,et al.  Iridium-catalyzed selective α-methylation of ketones with methanol. , 2014, Chemical communications.

[25]  Darren L. Poole,et al.  Rhodium-Catalyzed Ketone Methylation Using Methanol Under Mild Conditions: Formation of α-Branched Products** , 2013, Angewandte Chemie.

[26]  Feng Li,et al.  General and efficient method for direct N-monomethylation of aromatic primary amines with methanol , 2012 .

[27]  Paul Anastas,et al.  Green chemistry: principles and practice. , 2010, Chemical Society reviews.

[28]  Mark S. Sundrud,et al.  Halofuginone Inhibits TH17 Cell Differentiation by Activating the Amino Acid Starvation Response , 2009, Science.

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

[30]  T. Yakaiah,et al.  Synthesis of novel 4,6-disubstituted quinazoline derivatives, their anti-inflammatory and anti-cancer activity (cytotoxic) against U937 leukemia cell lines. , 2008, European journal of medicinal chemistry.

[31]  Robert A Dagle,et al.  Methanol steam reforming for hydrogen production. , 2007, Chemical reviews.

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

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

[34]  Michael Decker,et al.  Novel inhibitors of acetyl- and butyrylcholinesterase derived from the alkaloids dehydroevodiamine and rutaecarpine. , 2005, European journal of medicinal chemistry.

[35]  Jean-Paul Lange,et al.  Methanol synthesis: a short review of technology improvements , 2001 .

[36]  P. D. Cook,et al.  Structure-activity relationships of novel 2-substituted quinazoline antibacterial agents. , 1999, Journal of medicinal chemistry.

[37]  J. Chern,et al.  Pharmacological Activity of DC−015, a Novel Potent and Selective α1‐Adrenoceptor Antagonist , 1996 .

[38]  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.

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

[40]  Y. Obora,et al.  Conferences and Meetings , 1966, British medical journal.