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Eng., 3, 100089, 10.1016\u002Fj.cscee.2021.100089\nShi, 2022, Controllable synthesis of a hollow Cr2O3 electrocatalyst for enhanced nitrogen reduction toward ammonia synthesis, Chin. J. Chem. Eng., 41, 358, 10.1016\u002Fj.cjche.2021.11.016\nAbdullah, 2014, Structural and optical characterization of Cr2O3 nanostructures: Evaluation of its dielectric properties, Aip Adv., 4, 027121, 10.1063\u002F1.4867012\nMakhlouf, 2013, Structural, morphological and electrical properties of Cr2O3 nanoparticles, Mater. Sci. Eng., B, 178, 337, 10.1016\u002Fj.mseb.2013.01.012\nRybchynskyi, 2022, A good material for effectively removing a variety of pollutants in sewage: single-phase Cr2O3 nanoparticles, J. Agric. Environ. Sci., 2, 16\nWang, 2019, Solution combustion synthesis of Cr2O3 nanoparticles and the catalytic performance for dehydrofluorination of 1, 1, 1, 3, 3-pentafluoropropane to 1, 3, 3, 3-tetrafluoropropene, Molecules, 24, 361, 10.3390\u002Fmolecules24020361\nTsegay, 2021, Structural and optical properties of green synthesized Cr2O3 nanoparticles, Mater. Today:. Proc., 36, 587\nKhan, 2021, Green synthesis of chromium oxide nanoparticles for antibacterial, antioxidant anticancer, and biocompatibility activities, Int. J. Mol. Sci., 22, 502, 10.3390\u002Fijms22020502\nLima, 2006, Nanocrystalline Cr2O3 and amorphous CrO3 produced by solution combustion synthesis, J. Eur. Ceram. Soc., 26, 1213, 10.1016\u002Fj.jeurceramsoc.2005.01.042\nKazemi, 2022, Synthesis of a new hybrid material based on Cr2O3 nanoparticles encapsulating phosphotungstic acid as an efficient photocatalyst to degrade a synthetic opioid: methadone, Inorganic Chem. 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Preparation and characterization of Cr2O3 nanoparticle prepared by chemical method. In: AIP Conference Proceedings(Vol. 2213, No. 1, p. 020202). AIP Publishing LLC. doi: 10.1063\u002F5.0000124.\nGupta, 2014, Facile synthesis and characterization of nanostructured chromium oxide, Powder Technol., 254, 78, 10.1016\u002Fj.powtec.2014.01.014\nRoy, 2015, Solvothermal synthesis of Cr2O3 nanocubes via template-free route, Mater. Chem. Phys., 159, 101, 10.1016\u002Fj.matchemphys.2015.03.058\nPardo, 2017, Chromium oxide nanoparticles with controlled size prepared from hydrothermal chromium oxyhydroxide precursors, Ceram. Int., 43, 2756, 10.1016\u002Fj.ceramint.2016.11.104\nZhao, M., Zhu, H., Zhang, J., Li, M., Cai, Z., 2017, June. Synthesis and gas sensor application of nanostructure Cr2O3 hollow spheres. In: IOP Conference Series: Materials Science and Engineering (Vol. 207, No. 1, p. 012030). 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Mater., 190, 945, 10.1016\u002Fj.jhazmat.2011.04.029\nYanga, 2017, A novel visible-light –driven In-based MOF\u002Fgraphene oxide composite photocatayst with enhanced photocatalytic activity toward the degradation of amoxyline, Applied Catalysis B Environmental., 200, 673, 10.1016\u002Fj.apcatb.2016.07.057\nZhao, 2018, Lead-carboxylate\u002Fpolyiodide hybrids constructed from halogen bonding and asymmetric viologen: structures, visible-light-driven photocatalytic properties and enhanced photocurrent responses, CrystEngComm., 20, 2245, 10.1039\u002FC8CE00120K\nAbazari, 2021, PMo12@UiO-67 nanocomposite as a novel non-leaching catalyst with enhanced performance durability for sulfur removal from liquid fuels with exceptionally diluted oxidant, Applied Catalysis B: Environmental., 283, 119582, 10.1016\u002Fj.apcatb.2020.119582\nLi, 2020, Novel p-n Li2 SnO3 \u002Fg-C3 N4 Heterojunction with Enhanced Visible Light Photocatalytic Efficiency towards Rhodamine B Degradation, Front. 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1891, Chem. Ber., 24, 1317, 10.1002\u002Fcber.189102401228\nBiginelli, 1889, Gazz. Chim. Ital., 19, 212\nSahu, 2014, An efficient, reusable, and biodegradable catalyst for green synthesis of heterocycles, Indus. Eng. Chem. Res., 53, 2085, 10.1021\u002Fie402037d\nSahu, 2014, Role of surfactant and micelle-promoted mild, efficient, sustainable synthesis of 2-aminobenzothiazolomethyl naphthols and 5-(2-aminobenzothiazolomethyl)-6-hydroxyquinolines in water at room temperature, RSC Adv., 4, 40414, 10.1039\u002FC4RA03847A\nSahu, 2018, Metal-free construction of fused pyrimidines via consecutive C-C and C–N bond formation in water, ACS Omega, 3, 15035, 10.1021\u002Facsomega.8b01993\nMoradi, Ashraf; Heydari, Reza; Maghsoodlou, Malek Taher (2015).Agar: a novel, efficient, and biodegradable catalyst for the one-pot three-component and green synthesis of 2,3-dihydroquinazolin-4(1H)-one, 4H-pyrimidobenzothiazole and 2-aminobenzothiazolomethylnaphthol derivatives. Research on Chemical Intermediates, 2015, 41(10), 7377–7391.\nVaidya, 2016, Thiamine hydrochloride (VB1) as an efficient catalyst for the synthesis of 4H-pyrimido[2,1-b] benzothiazole derivatives, Chem. Biol. Interface, 6, 47\nBhoi, 2019, Novel benzothiazole containing 4H-pyrimido[2,1-b]benzothiazoles derivatives: One pot, solvent-free microwave assisted synthesis and their biological evaluation, Arab. J. Chem., 12, 3799, 10.1016\u002Fj.arabjc.2016.01.012\nJones, 1988, synthesis and antiviral properties of (E)-5-(2-bromovinyl)-2′-deoxycytidine-related compounds, J. Med. Chem., 31, 268, 10.1021\u002Fjm00396a043\nAgarwal, 2005, Synthesis of 2,4,6-trisubstituted pyrimidines as antimalarial agents, Bioorg. Med. Chem., 13, 4645, 10.1016\u002Fj.bmc.2005.04.061\nXie, 2009, Synthesis and biological evaluation of novel 2,4,5-substituted pyrimidine derivatives for anticancer activity, Bioorg. Med. Chem. Lett., 19, 275, 10.1016\u002Fj.bmcl.2008.09.067\nTozkoparan, 1999, Synthesis and anti-inflammatory activities of some thiazolo[3,2-a]pyrimidine derivatives, Farmaco, 54, 588, 10.1016\u002FS0014-827X(99)00068-3\nKappe, 1998, 4-aryldihydropyrimidines via the Biginelli condensation aza-analogs of Nifedipine type calcium channel modulate, Molecule, 3, 1, 10.3390\u002F30100001\nMethyl 2-methyl-4-phenyl-4H-pyrimido [2,1-b][1,3] benzothiazole-3-carboxylate (4a):To a mixture of benzaldehyde (2g; 18.8 mmol), 2-aminobenzothizole (2.83g; 18.8 mmol), methyl acetoacetate (2.19g; 18.8 mmol) in water added acetic acid (0.23g; 3.8 mmol) and activated charcoal (0.2g; 10% of aldehyde) into a round-bottom flask. Then the reaction mass heated up to 90-95 °C with continuous stirring at 90-95 °C for 2 h. The progress of reaction was monitored using TLC. On completion of the reaction (absence of aldehyde), reaction mass cooled to ambient temperature gently. Reaction mass diluted with methylene chloride and stirred for about 30 min. Reaction mass filtered through celite pad and then layers separated. Organic layer recovered completely under reduce pressure to get oily residue which further purified by column chromatography by eluted with ethyl acetate\u002Fhexane. Isolated material finally recrystallized in methanol, and dried under vacuum to afford yellowish solid (5.51g; 87%). Rf =0.6 (TLC mobile phase ethyl acetate: hexane = 4:6 v\u002Fv); M.pt 146.2 °C.",{"EN":571},"Extensive Biginelli reaction: Activated charcoal promoted green approach for one pot synthesis of 4H-pyrimido[2,1-b][1,3]benzothiazole-3-carboxylate derivatives",{"VOID":573},"10.1016\u002Fj.rechem.2023.100781","https:\u002F\u002Fwww.sciencedirect.com\u002Fscience\u002Farticle\u002Fpii\u002FS2211715623000206",[576,591],{"id":577,"sortIndex":19,"researcher":18,"roles":578,"affiliations":579,"properties":588},"fa23e876-2a08-447e-89d3-fb4b5589bd1d",[116],[580],{"id":18,"sortIndex":19,"affiliation":581,"properties":18},{"id":582,"createTime":583,"updateTime":583,"relativeEntities":584,"slug":18,"properties":585,"entityType":38,"verifyStatus":17,"verifyTime":18,"verifyNote":18,"syncStatus":17,"languages":18,"translateLanguages":18,"viewCount":19},"8e763c16-4682-4155-ae35-734c0388638c","2024-01-27T07:31:25.746+00:00",[],{"title":586},{"VI":587},"Organic Synthesis Laboratory, School of Engineering and Sciences (SOES), G D Goenka University, 122001 Gurugram, Haryana, India",{"title":589},{"VI":590},"Sourav Handique",{"id":592,"sortIndex":143,"researcher":18,"roles":593,"affiliations":594,"properties":600},"1cf446c4-7241-414e-8318-28fde956e9da",[116],[595],{"id":18,"sortIndex":19,"affiliation":596,"properties":18},{"id":582,"createTime":583,"updateTime":583,"relativeEntities":597,"slug":18,"properties":598,"entityType":38,"verifyStatus":17,"verifyTime":18,"verifyNote":18,"syncStatus":17,"languages":18,"translateLanguages":18,"viewCount":19},[],{"title":599},{"VI":587},{"title":601},{"VI":602},"Priyanka Sharma",{"url":574,"publisher":604,"properties":626},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":605,"slug":10,"properties":606,"entityType":16,"verifyStatus":17,"verifyTime":18,"verifyNote":18,"syncStatus":17,"languages":18,"translateLanguages":18,"viewCount":19,"subjectFields":609,"manageAffiliations":610,"indexDatabases":611,"url":18,"thumbnailPath":18,"statistic":18,"gsStatistic":18,"type":18,"analyzePriority":18},[],{"issn":607,"title":608},{"VOID":13},{"EN":15},[],[],[612,619],{"id":53,"indexDatabase":613,"url":66,"indexYears":67,"academicFieldIds":618,"indexDatabaseRanking":70},{"id":55,"createTime":56,"updateTime":57,"relativeEntities":614,"label":615,"description":616,"key":63,"publicationTags":617,"standard":18},[],{"EN":60,"VI":60},{"EN":60,"VI":62},[65],[69],{"id":72,"indexDatabase":620,"url":87,"indexYears":18,"academicFieldIds":625,"indexDatabaseRanking":18},{"id":74,"createTime":75,"updateTime":76,"relativeEntities":621,"label":622,"description":623,"key":83,"publicationTags":624,"standard":18},[],{"EN":79,"VI":79},{"VI":81,"EN":82},[85,86],[89],{"volume":627,"pages":629},{"VOID":628},"5",{"VOID":630},"100781","2023-01-01",{"id":633,"createTime":634,"updateTime":634,"relativeEntities":635,"slug":636,"properties":637,"entityType":107,"verifyStatus":17,"verifyTime":18,"verifyNote":18,"syncStatus":17,"languages":18,"translateLanguages":18,"viewCount":19,"primaryUrl":644,"fullTextUrl":18,"authors":645,"publicationType":154,"publisherRelationship":715,"citationCount":18,"citationInfo":18,"publishDate":268,"publishYear":269,"citationAnalyzeStatus":17,"lastCitationAnalyze":18,"indexDatabases":18,"openAccess":18,"references":18,"isForceReanalyzing":185},"8c8db44c-2c1f-4a6e-b8bd-efbac10f8e7f","2023-11-30T23:44:09.117+00:00",[],"Xanthomonadin-mediated-synthesis-of-biocidal-and-photo-protective-silver-nanoparticles-XP-AgNPs-",{"references":638,"title":640,"doi":642},{"VOID":639},"Jain, 2011, Extracellular biosynthesis and characterization of silver nanoparticles using Aspergillus flavus NJP08: a mechanism perspective, Nanoscale, 3, 635, 10.1039\u002FC0NR00656D\nHttps:\u002F\u002Fstatnano.com\u002Fnanomaterials, “Nanomaterials Database | STATNANO,” Statnano.Com. 2022.\nPatil, 2018, Phytosynthesized gold nanoparticles- Bacillus thuringiensis (Bt – GNP) formulation : a novel photo stable preparation against mosquito larvae, J. 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