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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 40, 2010 - Issue 9
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Original Articles

Simple and Efficient Synthesis of 2-Aryl-2,3-Dihydroquinolin-4(1H)-ones Using Silica Chloride as a New Catalyst Under Solvent-Free Conditions

M. Muthukrishnan Organic Chemistry Division, National Chemical Laboratory, Pune, IndiaCorrespondence[email protected]
,
M. Mujahid Organic Chemistry Division, National Chemical Laboratory, Pune, India
,
V. Punitharasu Organic Chemistry Division, National Chemical Laboratory, Pune, India
&
D. A. Dnyaneshwar Organic Chemistry Division, National Chemical Laboratory, Pune, India
Pages 1391-1398 | Received 19 Mar 2009, Published online: 07 Apr 2010

Citations (12)

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Xuxu Zheng, Heyan Jiang, Jingjing Xie, Zhongyi Yin & Haidong Zhang. (2013) Highly Efficient and Green Synthesis of Flavanones and Tetrahydroquinolones. Synthetic Communications 43:7, pages 1023-1029.
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Articles from other publishers (11)

Christopher S. Parry, Matthew D. Grossmann, Amy Thomas, Max M. Majireck, Eric W. Reinheimer & Charles E. Kriley. (2021) Alternative Synthesis and Structural Analysis of the Antioxidant and Antitumor Agent 2-(3,5-Dimethoxyphenyl)-2,3-Dihydroquinolin-4(1H)-One. Journal of Chemical Crystallography 52:1, pages 122-129.
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Jae In Lee. (2021) A review of the syntheses of flavanones, thioflavanones, and azaflavanones from 2'‐substituted chalcones. Bulletin of the Korean Chemical Society 43:1, pages 117-128.
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Larisa Politanskaya, Tatyana Rybalova, Olga Zakharova, Georgy Nevinsky & Evgeny Tretyakov. (2018) p-Toluenesulfonic acid mediated one-pot cascade synthesis and cytotoxicity evaluation of polyfluorinated 2-aryl-2,3-dihydroquinolin-4-ones and their derivatives. Journal of Fluorine Chemistry 211, pages 129-140.
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Lijun Min, Bin Pan & Yanlong Gu. (2016) Synthesis of Quinoline-Fused 1-Benzazepines through a Mannich-Type Reaction of a C,N-Bisnucleophile Generated from 2-Aminobenzaldehyde and 2-Methylindole. Organic Letters 18:3, pages 364-367.
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Chamseddine Derabli, Sara Mahdjoub, Raouf Boulcina, Boudjemaa Boumoud, Hocine Merazig & Abdelmadjid Debache. (2016) [C8dabco]Br: a mild and convenient catalyst for intramolecular cyclization of 2-aminochalcones to the corresponding 2-aryl-2,3-dihydroquinolin-4(1H)-ones. Chemistry of Heterocyclic Compounds 52:2, pages 99-103.
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Dan Mao, Jun Tang, Wenbo Wang, Xin Liu, Shengying Wu, Jianjun Yu & Limin Wang. (2015) A Sc(OTf) 3 -catalyzed cascade reaction of o-aminoacetophenone with methanamine: construction of dibenzo[b,h][1,6]naphthyridine derivatives . Organic & Biomolecular Chemistry 13:7, pages 2122-2128.
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Kuppusamy Kanagaraj & Kasi Pitchumani. (2012) Per-6-amino-β-cyclodextrin as a Chiral Base Catalyst Promoting One-Pot Asymmetric Synthesis of 2-Aryl-2,3-dihydro-4-quinolones. The Journal of Organic Chemistry 78:2, pages 744-751.
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Yu‐Ying Ye, Lian‐Biao Zhao, Shu‐Chun Zhao, Fang Yang, Xue‐Yuan Liu & Yong‐Min Liang. (2012) Highly Regioselective Synthesis of Polysubstituted Tetrahydroquinolines by an Iodine‐Induced Tandem Cyclization Reaction from Propargylic Alcohols and Amines. Chemistry – An Asian Journal 7:9, pages 2014-2018.
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Anka Pejović, Ivan Damljanović, Dragana Stevanović, Mirjana Vukićević, Sladjana B. Novaković, Goran A. Bogdanović, Niko Radulović & Rastko D. Vukićević. (2012) Antimicrobial ferrocene containing quinolinones: Synthesis, spectral, electrochemical and structural characterization of 2-ferrocenyl-2,3-dihydroquinolin-4(1H)-one and its 6-chloro and 6-bromo derivatives. Polyhedron 31:1, pages 789-795.
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V. Kameswara Rao, M. Sudershan Rao & Anil Kumar. (2011) Ytterbium(III) triflate: An efficient and simple catalyst for isomerization of 2′‐hydroxychalcone and 2′‐aminochalcones in ionic liquid. Journal of Heterocyclic Chemistry 48:6, pages 1356-1360.
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M. Muthukrishnan, M. Mujahid, V. Punitharasu & D. A. Dnyaneshwar. (2010) ChemInform Abstract: Simple and Efficient Synthesis of 2-Aryl-2,3-dihydroquinolin-4(1H)-ones Using Silica Chloride as a New Catalyst under Solvent-Free Conditions.. ChemInform 41:40, pages no-no.
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