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Jin Zhang, Decheng Ren, Yangmin Ma, Weitao Wang, Hao Wu (2014)
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 ethanolTetrahedron, 70
M. Abdollahi-Alibeik, E. Shabani (2011)
Synthesis of 2,3-dihydroquinazolin-4(1H)-ones catalyzed by zirconium (IV) chloride as a mild and efficient catalystChinese Chemical Letters, 22
Jian Wu, Xianlin Du, Juan Ma, Yuping Zhang, Qingcai Shi, Lijun Luo, B. Song, Song Yang, D. Hu (2014)
Preparation of 2,3-dihydroquinazolin-4(1H)-one derivatives in aqueous media with β-cyclodextrin-SO3H as a recyclable catalystGreen Chemistry, 16
A. Ghorbani‐Choghamarani, Masoomeh Norouzi (2014)
Synthesis of copper (II)-supported magnetic nanoparticle and study of its catalytic activity for the synthesis of 2,3-dihydroquinazolin-4(1H)-onesJournal of Molecular Catalysis A-chemical, 395
B. Wood, W. Holzapfel (1999)
The Genera of Lactic Acid Bacteria
M. Kangani, N. Hazeri, M. Maghsoodlou, Khatereh Khandan-Barani, Maryam Kheyrollahi, Fereshteh Nezhadshahrokhabadi (2014)
Green procedure for the synthesis of 1,4-dihydropyrano[2,3-c]pyrazoles using saccharoseJournal of the Iranian Chemical Society, 12
A. Katritzky, C. Rees, E. Scriven (1996)
Comprehensive Heterocyclic Chemistry IV
B. Datta, M. Pasha (2012)
Glycine catalyzed convenient synthesis of 2-amino-4H-chromenes in aqueous medium under sonic condition.Ultrasonics sonochemistry, 19 4
Someshwar Dindulkar, Jeong-Geun Oh, V. Arole, Y. Jeong (2014)
Supported ceric ammonium nitrate: A highly efficient catalytic system for the synthesis of diversified 2,3-substituted 2,3-dihydroquinazolin-4(1H)-onesComptes Rendus Chimie, 17
JA Joule, K Mills (2000)
Heterocyclic Chemistry
A. Rostami, A. Tavakoli (2011)
Sulfamic acid as a reusable and green catalyst for efficient and simple synthesis of 2-substituted-2,3-dihydroquinazolin-4(1H)-ones in water or methanolChinese Chemical Letters, 22
M. Hour, Li‐Jiau Huang, Sheng‐Chu Kuo, Yi Xia, K. Bastow, Yuka Nakanishi, Ernest Hamel, Kuo Lee (2000)
6-Alkylamino- and 2,3-dihydro-3'-methoxy-2-phenyl-4-quinazolinones and related compounds: their synthesis, cytotoxicity, and inhibition of tubulin polymerization.Journal of medicinal chemistry, 43 23
A. Rostami, Bahman Tahmasbi, H. Gholami, Hajir Taymorian (2013)
Supported N-propylsulfamic acid on magnetic nanoparticles used as recoverable and recyclable catalyst for the synthesis of 2,3-dihydroquinazolin-4(1H)-ones in waterChinese Chemical Letters, 24
Vilas Labade, Pravin Shinde, M. Shingare (2013)
A facile and rapid access towards the synthesis of 2,3-dihydroquinazolin-4(1H)-onesTetrahedron Letters, 54
M. Singh, N. Raghav (2015)
2,3-Dihydroquinazolin-4(1H)-one derivatives as potential non-peptidyl inhibitors of cathepsins B and H.Bioorganic chemistry, 59
A. Rao, R. Bahekar (1999)
SYNTHESIS OF BENZIMIDAZO1,2-CQUINAZOLINES AS POSSIBLE BRONCHODILATORSIndian Journal of Chemistry Section B-organic Chemistry Including Medicinal Chemistry, 38
Yi Xia, Zhengyu Yang, M. Hour, S. Kuo, P. Xia, K. Bastow, Y. Nakanishi, P. Nampoothiri, T. Hackl, E. Hamel, K. Lee (2001)
Antitumor agents. Part 204: synthesis and biological evaluation of substituted 2-aryl quinazolinones.Bioorganic & medicinal chemistry letters, 11 9
B. Chen, Ji-tai Li, Guofeng Chen (2015)
Efficient synthesis of 2,3-disubstituted-2,3-dihydroquinazolin-4(1H)-ones catalyzed by dodecylbenzenesulfonic acid in aqueous media under ultrasound irradiation.Ultrasonics sonochemistry, 23
R. Sheldon (2005)
Green solvents for sustainable organic synthesis: state of the artGreen Chemistry, 7
M. Narasimhulu, Y. Lee (2011)
Ethylenediamine diacetate-catalyzed three-component reaction for the synthesis of 2,3-dihydroquinazolin-4(1H)-ones and their spirooxindole derivativesTetrahedron, 67
M. Gawande, V. Bonifácio, R. Luque, P. Branco, R. Varma (2013)
Benign by design: catalyst-free in-water, on-water green chemical methodologies in organic synthesis.Chemical Society reviews, 42 12
J. Safari, Soheila Gandomi-Ravandi (2014)
Efficient synthesis of 2-aryl-2,3-dihydroquinazolin-4(1H)-ones in the presence of nanocomposites under microwave irradiationJournal of Molecular Catalysis A-chemical, 390
Tao-Li Deng, Hongjun Wang, C. Cai (2015)
Highly enantioselective synthesis of dihydroquinazolinones through Sc(OTf)3-catalyzed intramolecular amidation of iminesJournal of Fluorine Chemistry, 169
S. Santra, Matiur Rahman, A. Roy, A. Majee, A. Hajra (2014)
Nano-indium oxide: An efficient catalyst for one-pot synthesis of 2,3-dihydroquinazolin-4(1H)-ones with a greener prospectCatalysis Communications, 49
Lin He, Haoquan Li, Jianbin Chen, Xiao‐Feng Wu (2014)
Recent advances in 4(3H)-quinazolinone synthesesRSC Advances, 4
M. Mousavi, N. Hazeri, M. Maghsoodlou, Sajjad Salahi, S. Habibi‐Khorassani (2013)
Entirely green protocol for the synthesis of β-aminoketones using saccharose as a homogenous catalystChinese Chemical Letters, 24
Jiuxi Chen, Deng-Ze Wu, F. He, Miao-chang Liu, Hua-yue Wu, Jinchang Ding, W. Su (2008)
Gallium(III) triflate-catalyzed one-pot selective synthesis of 2,3-dihydroquinazolin-4(1H)-ones and quinazolin-4(3H)-onesTetrahedron Letters, 49
P. Murthy, D. Rambabu, G. Krishna, C. Reddy, K. Prasad, M. Rao, M. Pal (2012)
Amberlyst-15 mediated synthesis of 2-substituted 2,3-dihydroquinazolin-4(1H)-ones and their crystal structure analysisTetrahedron Letters, 53
M. Kangani, N. Hazeri, M. Maghsoodlou (2017)
Synthesis of pyrrole and furan derivatives in the presence of lactic acid as a catalystJournal of Saudi Chemical Society, 21
P. Sahu, P. Sahu, S. Gupta, D. Agarwal (2014)
Chitosan: An Efficient, Reusable, and Biodegradable Catalyst for Green Synthesis of HeterocyclesIndustrial & Engineering Chemistry Research, 53
K. Ramesh, K. Karnakar, G. Satish, K. Reddy, Y. Nageswar (2012)
Tandem supramolecular synthesis of substituted 2-aryl-2,3-dihydroquinazolin-4(1H)-ones in the presence of β-cyclodextrin in waterTetrahedron Letters, 53
Yijia Chen, W. Shan, Min Lei, Lihong Hu (2012)
Thiamine hydrochloride (VB1) as an efficient promoter for the one-pot synthesis of 2,3-dihydroquinazolin-4(1H)-onesTetrahedron Letters, 53
Yanlong Gu (2012)
Multicomponent reactions in unconventional solvents: state of the artGreen Chemistry, 14
N. Hazeri, M. Maghsoodlou, Fatemeh Mir, M. Kangani, H. Saravani, Ebrahim Molashahi (2014)
An efficient one-pot three-component synthesis of tetrahydrobenzo[ b ]pyran and 3,4-dihydropyrano[ c ]chromene derivatives using starch solution as catalystChinese Journal of Catalysis, 35
M. Desroses, M. Scobie, T. Helleday (2013)
A new concise synthesis of 2,3-dihydroquinazolin-4(1H)-one derivativesNew Journal of Chemistry, 37
A. Rao, B. Vykunteswararao, T. Bhaskarkumar, Nivrutti Jogdand, D. Kalita, J. Lilakar, V. Siddaiah, P. Sanasi, A. Raghunadh (2015)
Sulfonic acid functionalized Wang resin (Wang-OSO3H) as polymeric acidic catalyst for the eco-friendly synthesis of 2,3-dihydroquinazolin-4(1H)-onesTetrahedron Letters, 56
M. Dabiri, P. Salehi, Somayeh Otokesh, M. Baghbanzadeh, G. Kozehgary, A. Mohammadi (2005)
Efficient synthesis of mono- and disubstituted 2,3-dihydroquinazolin-4(1H)-ones using KAl(SO4)2·12H2O as a reusable catalyst in water and ethanolTetrahedron Letters, 46
A. Davoodnia, S. Allameh, A. Fakhari, N. Tavakoli-Hoseini (2010)
Highly efficient solvent-free synthesis of quinazolin-4(3H)-ones and 2,3-dihydroquinazolin-4(1H)-ones using tetrabutylammonium bromide as novel ionic liquid catalystChinese Chemical Letters, 21
1 2 NH NH 20 mol% lactic acid NH H 1 O R R 1 2 solvent-free 70°C N O NH OAC Electronic supplementary material The online version of this article (doi:10.1007/s11164-016-2469-z) contains supplementary material, which is available to authorized users. & Nourallah Hazeri nhazeri@chem.usb.ac.ir Department of Chemistry, University of Sistan and Baluchestan, P. O. Box 98135-674, Zahedan, Iran 123 6382 S. Zhaleh et al. Keywords Green synthesis Lactic acid 2,3-Dihydroquinazolin-4(1H)-one Solvent-free Introduction Synthesis of biologically and pharmacologically active organic compounds has drawn much attention in recent years; among them, nitrogen-containing hetero- cyclic compounds are of importance due to their applications in many biological processes as markers or messenger molecules and also their use as agrochemicals and pharmaceuticals [1, 2]. 2,3-Dihydroquinazolin-4(1H)-ones are a series of six- membered, nitrogen-containing heterocyclic compounds that display a wide spectrum of biological and pharmacological activities as well as medicinal properties including anticancer [3], antitumor [4], antibiotic [5], and antihyperten- sion action [6]. Some examples of drugs possessing quinazolinone skeleton are shown in Fig. 1. Additionally, 2,3-dihydroquinazolinones are valuable synthetic intermediates for preparation of biologically active 4(3H)-quinazolinones by oxidation [7]. Two main methods, viz. (1) condensation of aldehyde or ketone with 2-aminobenzamide and
Research on Chemical Intermediates – Springer Journals
Published: Feb 8, 2016
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