Visible light-induced one-pot three-component synthesis of quinazolines under catalyst-free condition
暂无分享,去创建一个
Yuqi Pang | Qidi Zhong | Wuji Sun | Dongmei Li | Xue‐Rong Chen | Xue Ma | Letian Ying
[1] G. Psomas,et al. Transition metal(II) complexes of halogenated derivatives of (E)-4-(2-(pyridin-2-ylmethylene)hydrazinyl)quinazoline: structure, antioxidant activity, DNA-binding DNA photocleavage, interaction with albumin and in silico studies. , 2022, Dalton Transactions.
[2] R. Tuxworth,et al. Inhibition of Chk2 promotes neuroprotection, axon regeneration, and functional recovery after CNS injury , 2022, Science advances.
[3] Q. Fan,et al. Straightforward synthesis of quinazolin-4(3H)-ones via visible light-induced condensation cyclization , 2022, RSC advances.
[4] Neelima Mahato,et al. Recent Advances on Quinazoline Derivatives: A Potential Bioactive Scaffold in Medicinal Chemistry , 2021, ChemEngineering.
[5] Q. Fan,et al. Catalyst-free visible-light mediated selective oxidation of sulfides into sulfoxides under clean conditions , 2021, Green Chemistry.
[6] Xue-Meng Wang,et al. Synthesis of benzothiazoles using fluorescein as an efficient photocatalyst under visible light , 2021, Molecular Catalysis.
[7] Xiao‐Feng Wu,et al. Palladium-catalyzed carbonylative synthesis of quinazolines: Silane act as better nucleophile than amidine , 2021, Molecular Catalysis.
[8] Jorge Quintero-Saumeth,et al. Biologically Active Quinoline‐Hydrazone Conjugates as Potential Trypanosoma cruzi DHFR‐TS Inhibitors: Docking, Molecular Dynamics, MM/PBSA and Drug‐Likeness Studies , 2021 .
[9] Cheng‐Chung Wang,et al. TMSOTf-catalyzed synthesis of substituted quinazolines using hexamethyldisilazane as a nitrogen source under neat and microwave irradiation conditions. , 2020, Organic & biomolecular chemistry.
[10] N. Azas,et al. Synthesis and Antiplasmodial Evaluation of 4-Carboxamido- and 4-Alkoxy-2-Trichloromethyl Quinazolines , 2020, Molecules.
[11] N. Curtin,et al. DNA damage checkpoint kinases in cancer , 2020, Expert Reviews in Molecular Medicine.
[12] D. S. Bose,et al. A convenient access to 2,4-disubstituted quinazolines via one-pot three-component reaction under mild conditions† , 2020, Synthetic Communications.
[13] Bo Xu,et al. A two-dimensional quinazoline based covalent organic framework with a suitable direct gap and superior optical absorption for photovoltaic applications , 2020 .
[14] Qingbin Meng,et al. Direct C–H difluoromethylation of heterocycles via organic photoredox catalysis , 2020, Nature Communications.
[15] A. Gemma,et al. Gefitinib Alone Versus Gefitinib Plus Chemotherapy for Non-Small-Cell Lung Cancer With Mutated Epidermal Growth Factor Receptor: NEJ009 Study. , 2020, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[16] A. Gemma,et al. Erlotinib plus bevacizumab versus erlotinib alone in patients with EGFR-positive advanced non-squamous non-small-cell lung cancer (NEJ026): interim analysis of an open-label, randomised, multicentre, phase 3 trial. , 2019, The Lancet. Oncology.
[17] Chae S. Yi,et al. Synthesis of Quinazoline and Quinazolinone Derivatives via Ligand-Promoted Ruthenium-Catalyzed Dehydrogenative and Deaminative Coupling Reaction of 2-Aminophenyl Ketones and 2-Aminobenzamides with Amines. , 2019, Organic letters.
[18] S. Sinha,et al. Dehydrogenative Synthesis of Quinolines, 2-Aminoquinolines, and Quinazolines Using Singlet Diradical Ni(II)-Catalysts. , 2019, The Journal of organic chemistry.
[19] O. Chupakhin,et al. Functionalized Quinazolines and Pyrimidines for Optoelectronic Materials , 2018, Current Organic Synthesis.
[20] A. Lei,et al. Electrochemical Acceptorless Dehydrogenation of N-Heterocycles Utilizing TEMPO as Organo-Electrocatalyst , 2018 .
[21] T. Mohamed,et al. 2,4-Disubstituted quinazolines as amyloid-β aggregation inhibitors with dual cholinesterase inhibition and antioxidant properties: Development and structure-activity relationship (SAR) studies. , 2017, European journal of medicinal chemistry.
[22] Yang Fan,et al. Heterogeneous Palladium‐Catalyzed Hydrogen‐Transfer Cyclization of Nitroacetophenones with Benzylamines: Access to C−N Bonds , 2016 .
[23] G. Deng,et al. Lewis acid-catalyzed 2-arylquinazoline formation from N′-arylbenzimidamides and paraformaldehyde , 2016 .
[24] N. Azas,et al. Looking for new antiplasmodial quinazolines: DMAP-catalyzed synthesis of 4-benzyloxy- and 4-aryloxy-2-trichloromethylquinazolines and their in vitro evaluation toward Plasmodium falciparum. , 2016, European journal of medicinal chemistry.
[25] K. Skubi,et al. Dual Catalysis Strategies in Photochemical Synthesis , 2016, Chemical reviews.
[26] G. Khodarahmi,et al. Quinazolinone and quinazoline derivatives: recent structures with potent antimicrobial and cytotoxic activities , 2016, Research in pharmaceutical sciences.
[27] Jieping Zhu,et al. Cross-Coupling Hydrogen Evolution by Visible Light Photocatalysis Toward C(sp(2))-P Formation: Metal-Free C-H Functionalization of Thiazole Derivatives with Diarylphosphine Oxides. , 2016, Organic letters.
[28] Yanmei Zhang,et al. Synthesis and Evaluation of Novel Erlotinib-NSAID Conjugates as More Comprehensive Anticancer Agents. , 2015, ACS medicinal chemistry letters.
[29] S. Saad,et al. A new and facile CuCl2·2H2O-catalyzed one-pot three-component synthesis for quinazolines , 2015, Monatshefte für Chemie - Chemical Monthly.
[30] B. Green. Prazosin in the Treatment of PTSD , 2014, Journal of psychiatric practice.
[31] S. Bari,et al. Quinazolines: new horizons in anticonvulsant therapy. , 2014, European journal of medicinal chemistry.
[32] A. Saeed,et al. Recent advances in the structural library of functionalized quinazoline and quinazolinone scaffolds: synthetic approaches and multifarious applications. , 2014, European journal of medicinal chemistry.
[33] L. Shaw,et al. Antibacterial activity of a series of N2,N4-disubstituted quinazoline-2,4-diamines. , 2014, Journal of medicinal chemistry.
[34] S. Saha,et al. I2-Catalyzed three-component protocol for the synthesis of quinazolines , 2012 .
[35] P. Pratap,et al. DDQ/TBHP-Induced Oxidative Cyclization Process: A Metal-Free Approach for the Synthesis of 2-Phenylquinazolines , 2012 .
[36] Xiao‐Nan Zhang,et al. Catalyst-free synthesis of quinazoline derivatives using low melting sugar–urea–salt mixture as a solvent , 2012 .
[37] A. Thangamani. Regiospecific synthesis and biological evaluation of spirooxindolopyrrolizidines via [3+2] cycloaddition of azomethine ylide. , 2010, European journal of medicinal chemistry.
[38] A. Kadi,et al. Synthesis, analgesic and anti-inflammatory evaluation of some novel quinazoline derivatives. , 2010, European journal of medicinal chemistry.
[39] N. Fujii,et al. Direct synthesis of quinazolines through copper-catalyzed reaction of aniline-derived benzamidines. , 2010, Organic letters.
[40] Anren Hu,et al. Antimicrobial study of newly synthesized 6-substituted indolo[1,2-c]quinazolines. , 2010, European journal of medicinal chemistry.
[41] U. Murthy,et al. Synthesis of multisubstituted quinolines from Baylis-Hillman adducts obtained from substituted 2-chloronicotinaldehydes and their antimicrobial activity. , 2006, Bioorganic & medicinal chemistry.
[42] P. Guiry,et al. Synthesis of Quinazolinones and Quinazolines , 2005 .
[43] E. Peskind,et al. Reduction of nightmares and other PTSD symptoms in combat veterans by prazosin: a placebo-controlled study. , 2003, The American journal of psychiatry.
[44] Corey R J Stephenson,et al. Visible light photoredox catalysis: applications in organic synthesis. , 2011, Chemical Society reviews.
[45] J. Michael. Quinoline, quinazoline and acridone alkaloids. , 2008, Natural product reports.