Works matching DE "PYRIMIDINE synthesis"
Results: 391
The pyrimidine biosynthetic pathway and its regulation in Pseudomonas jessenii.
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- Antonie van Leeuwenhoek, 2019, v. 112, n. 3, p. 461, doi. 10.1007/s10482-018-1168-8
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Evolution of Cyclic Amidohydrolases: A Highly Diversified Superfamily.
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- Journal of Molecular Evolution, 2013, v. 77, n. 3, p. 70, doi. 10.1007/s00239-013-9580-1
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Synthesis and Structure of Drimane Sesquiterpenoids Containing Pyrimidine, Pyrazine, 1,2,4-triazole, and Carbazole Rings.
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- Chemistry of Natural Compounds, 2018, v. 54, n. 3, p. 455, doi. 10.1007/s10600-018-2378-z
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Functionalization of 2-Amino-3-benzyl-6-(benzylthio)pyrimidin-4(3H)-one: An Efficient Access to the Synthesis of Polycyclic Pyrimidine Scaffolds.
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- Russian Journal of General Chemistry, 2020, v. 90, n. 3, p. 489, doi. 10.1134/S107036322003024X
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A Facile Synthesis of Polycyclic Pyrimidine Fluorophores via Inter- and Intramolecular Cyclization of Activated 2-Amino-3,6-disubstitued Pyrimidin-4-ones.
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- Russian Journal of General Chemistry, 2020, v. 90, n. 1, p. 148, doi. 10.1134/S1070363220010235
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Synthesis of New Fused Thieno[3,2-d]pyrimidines Based on Thieno[3,2-d][1,3]oxazine Derivative.
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- Russian Journal of General Chemistry, 2019, v. 89, n. 4, p. 847, doi. 10.1134/S1070363219040340
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Synthesis, Antitubercular Activity, and Molecular Docking Studies of Novel 2-(4-Chlorobenzylamino)-4-(cyclohexylmethylamino)-pyrimidine-5-carboxamides.
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- Russian Journal of General Chemistry, 2019, v. 89, n. 4, p. 836, doi. 10.1134/S1070363219040327
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Efficient Synthesis of New Pyrimido[5′,4′:5,6]pyrano[2,3-d]pyrimidine-2,4,6(1H,3H)-triones via the Tandem Intramolecular Pinner–Dimroth Rearrangement, and Their Antibacterial Activity.
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- Russian Journal of General Chemistry, 2018, v. 88, n. 12, p. 2658, doi. 10.1134/S1070363218120290
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Synthesis and Anti-HBV Activity of Novel Substituted Pyrimidine Glycosides and Their Acyclic Analogues.
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- Russian Journal of General Chemistry, 2018, v. 88, n. 8, p. 1734, doi. 10.1134/S1070363218080285
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New nitrogen heterocycles containing a ferrocene fragment: Optical and physicochemical properties.
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- Russian Journal of General Chemistry, 2017, v. 87, n. 3, p. 470, doi. 10.1134/S1070363217030161
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Synthesis of 6-methyl-2-[2-phenyl-2-(arylhydrazono)ethyl]-3 Н-pyrimidine-4-ones and their oxidation by hydrogen peroxide and selenium dioxide.
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- Russian Journal of General Chemistry, 2016, v. 86, n. 7, p. 1604, doi. 10.1134/S1070363216070112
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Aryl ethers of 4-[(2-hydroxyethyl)sulfanyl]pyrimidine derivatives: Pathways of synthesis and fungicidal activity of their salt forms.
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- Russian Journal of General Chemistry, 2016, v. 86, n. 6, p. 1274, doi. 10.1134/S1070363216060098
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Synthesis of novel 2,4,6-trisubstituted pyrimidine derivatives and their in vitro antimicrobial activity.
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- Russian Journal of General Chemistry, 2016, v. 86, n. 6, p. 1396, doi. 10.1134/S1070363216060268
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Synthesis and biological activity of hydrochlorides of benzyl ethers of pyrimidin-4(3 H)-thiones and related compounds.
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- Russian Journal of General Chemistry, 2015, v. 85, n. 1, p. 79, doi. 10.1134/S1070363215010144
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A simple approach to the synthesis of 2-(2-amino-4-arylthiazol-5-yl)pyrimidines.
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- Russian Journal of General Chemistry, 2013, v. 83, n. 3, p. 526, doi. 10.1134/S1070363213030195
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Synthesis of 4-alkyl-2-aryl-1,3-oxazole[5,4- d]pyrimidine-7(4 H)-thiones and 6-alkyl-2-aryl-1,3-oxazole[5,4- d]pyrimidin-7(6 H)-ones from 2-aroylamino-3,3-dichloroacrylonitriles.
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- Russian Journal of General Chemistry, 2012, v. 82, n. 4, p. 739, doi. 10.1134/S1070363212040226
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The First Catalytic Direct C–H Arylation on C2 and C3 of Thiophene Ring Applied to Thieno-Pyridines, -Pyrimidines and -Pyrazines.
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- Catalysts (2073-4344), 2018, v. 8, n. 4, p. 137, doi. 10.3390/catal8040137
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Synthesis, Spectral Characterization & Antimicrobial Evaluation of Some Novel Pyrimidine-2,4(1H,3H)-diones.
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- Indo Global Journal of Pharmaceutical Sciences, 2012, v. 2, n. 1, p. 70, doi. 10.35652/igjps.2012.07
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Synthesis and Pharmacological Activities of Pyrano[2,3-d]pyrimidine and Pyrano[2,3-d]pyrimidine-5-one Derivatives as New Fused Heterocyclic Systems.
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- Journal of Chemistry, 2017, p. 1, doi. 10.1155/2017/5373049
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Design, Synthesis, and In Vitro Antimicrobial Evaluation of Fused Pyrano[3,2-e]tetrazolo[1,5-c]pyrimidines and Diazepines.
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- ISRN Organic Chemistry, 2013, p. 1, doi. 10.1155/2013/635384
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An Efficient One-Pot Green Protocol for the Synthesis of 5-Unsubstituted 3,4-Dihydropyrimidin-2(1H)-Ones Using Recyclable Amberlyst 15 DRY as a Heterogeneous Catalyst via Three-Component Biginelli-Like Reaction.
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- ISRN Organic Chemistry, 2012, p. 1, doi. 10.5402/2012/480989
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Synthesis of 3,4-Dihydropyrimidin-2(1H)-Ones and Their Corresponding 2(1H)Thiones Using Trichloroacetic Acid as a Catalyst under Solvent-Free Conditions.
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- ISRN Organic Chemistry, 2012, p. 1, doi. 10.5402/2012/474626
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A Green, Expeditious, One-Pot Synthesis of 3, 4-Dihydropyrimidin-2(1H)-ones Using a Mixture of Phosphorus Pentoxide-Methanesulfonic Acid at Ambient Temperature.
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- ISRN Organic Chemistry, 2012, p. 1, doi. 10.5402/2012/415645
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SYNTHESIS OF PYRROLIDINES AND TETRAHYDROPYRIMIDINES VIA ONE-POT AND THREE COMPONENT CASCADE COUPLING STRATEGY IN WATER.
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- Rasayan Journal of Chemistry, 2017, v. 10, n. 1, p. 6, doi. 10.7324/RJC.2017.1011545
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SYNTHESIS OF PYRIMIDINE CARBOXAMIDE DERIVATIVES CATALYZED BY URANYL NITRATE HEXA HYDRATE WITH THEIR ANTIBACTERIAL AND ANTIOXIDANT STUDIES.
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- Bulletin of the Chemical Society of Ethiopia, 2016, v. 30, n. 1, p. 119, doi. 10.4314/bcse.v30i1.11
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Synthesis of Some Benzofuran Derivatives Containing Pyrimidine Moiety as Potent Antimicrobial Agents.
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- Iranian Journal of Pharmaceutical Research, 2018, v. 17, n. 1, p. 75
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Design and Synthesis of New Benzimidazole and Pyrimidine Derivatives as α-glucosidase Inhibitor.
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- Iranian Journal of Pharmaceutical Research, 2015, v. 14, n. 3, p. 723
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Multicomponent Strategy for the Preparation of Pyrrolo[1,2- a]pyrimidine Derivatives under Catalyst-Free and Microwave Irradiation Conditions.
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- Chinese Journal of Chemistry, 2016, v. 34, n. 7, p. 696, doi. 10.1002/cjoc.201600142
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Synthesis and Structure of Azacalix[2]pyrimidine[2]triazines and Their Self-assembly in the Solid State.
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- Chinese Journal of Chemistry, 2014, v. 32, n. 10, p. 1033, doi. 10.1002/cjoc.201400505
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Diastereoselective Synthesis of Functionalized Tetrahydropyrimidin-2-thiones via ZnCl<sub>2</sub> Promoted One-pot Reactions.
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- Chinese Journal of Chemistry, 2014, v. 32, n. 2, p. 172, doi. 10.1002/cjoc.201300577
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Pyrimidines as block units in heterocycles: novel synthesis of pyrimidines and condensed pyrimidine derivatives.
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- Journal of the Iranian Chemical Society, 2019, v. 16, n. 11, p. 2451, doi. 10.1007/s13738-019-01712-4
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Nanoparticles of manganese oxides as efficient catalyst for the synthesis of pyrano[2,3- d]pyrimidine derivatives and their complexes as potent protease inhibitors.
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- Journal of the Iranian Chemical Society, 2018, v. 15, n. 2, p. 431, doi. 10.1007/s13738-017-1244-4
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Nano-sawdust-OSOH as a new, cheap and effective nanocatalyst for one-pot synthesis of pyrano[2,3- d]pyrimidines.
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- Journal of the Iranian Chemical Society, 2015, v. 12, n. 10, p. 1801, doi. 10.1007/s13738-015-0655-3
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Heterocyclization of thiouracil derivative: synthesis of thiazolopyrimidines, tetrazolopyrimidines and triazolopyrimidines of potential biological activity.
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- Journal of the Iranian Chemical Society, 2015, v. 12, n. 10, p. 1809, doi. 10.1007/s13738-015-0656-2
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Efficient synthesis of novel imidazo[1,2-a]pyrimidine derivatives via one-pot three-component procedure.
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- Journal of the Iranian Chemical Society, 2015, v. 12, n. 6, p. 1049, doi. 10.1007/s13738-014-0564-x
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Synthesis and in vitro and in vivo antitumor/anticancer activity of novel O-Mannich bases of 4,6-diaryl-3,4-dihydropyrimidine-2(1 H)-ones.
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- Journal of the Iranian Chemical Society, 2014, v. 11, n. 6, p. 1619, doi. 10.1007/s13738-014-0438-2
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Solvent-free synthesis of polyfunctional tetrahydropyrimidines promoted by recyclable ionic liquid.
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- Journal of the Iranian Chemical Society, 2013, v. 10, n. 4, p. 695, doi. 10.1007/s13738-012-0202-4
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Microwave promoted improved regioselective synthesis of 1 H,3 H,6 H[2]benzopyrano[4,3- d]pyrimidine-2,4-diones by radical cyclisation.
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- Journal of the Iranian Chemical Society, 2013, v. 10, n. 1, p. 55, doi. 10.1007/s13738-012-0171-7
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Water-mediated synthesis of disubstituted 5-aminopyrimidines from vinyl azides under microwave irradiation.
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- Green Chemistry Letters & Reviews, 2018, v. 11, n. 2, p. 62, doi. 10.1080/17518253.2018.1437225
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Efficient and environmentally benign synthetic protocol for the synthesis of structurally diverse annulated pyridopyrimidines.
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- Green Chemistry Letters & Reviews, 2014, v. 7, n. 1, p. 37, doi. 10.1080/17518253.2014.895057
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Green chemistry multicomponent protocol for formylation and Knoevenagel condensation for synthesis of (Z)-5-arylaminomethylene pyrimidine 2, 4, 6-trione derivatives in water.
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- Green Chemistry Letters & Reviews, 2014, v. 7, n. 1, p. 1, doi. 10.1080/17518253.2013.869839
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Rational Design and Synthesis of Diverse Pyrimidine Molecules Bearing Sulfonamide Moiety as Novel ERK Inhibitors.
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- International Journal of Molecular Sciences, 2019, v. 20, n. 22, p. 5592, doi. 10.3390/ijms20225592
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A critical review of the reproductive safety of Leflunomide.
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- Clinical Rheumatology, 2020, v. 39, n. 2, p. 607, doi. 10.1007/s10067-019-04819-4
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Synthesis and Hypotensive Activity of Pyrimidine-2,4-(1 H,3 H)-Dione Derivatives Containing Thietane Rings with Sulfur in Various Oxidation States.
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- Pharmaceutical Chemistry Journal, 2014, v. 48, n. 7, p. 434, doi. 10.1007/s11094-014-1126-3
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Synthesis and Antioxidant Activity of 2-Thioxo-1,2,3,4-Tetrahydropyrimidine-5-Carbamides.
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- Pharmaceutical Chemistry Journal, 2014, v. 48, n. 4, p. 246, doi. 10.1007/s11094-014-1087-6
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Synthesis and Antitumor and Antibacterial Properties of New N-Alkylated Pyrimidines.
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- Pharmaceutical Chemistry Journal, 2013, v. 47, n. 6, p. 303, doi. 10.1007/s11094-013-0948-8
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Synthesis and Neurotropic Activity of New Condensed Pyrido[3′,2′:4,5]furo[3,2- d]-pyrimidine Derivatives.
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- Pharmaceutical Chemistry Journal, 2013, v. 47, n. 3, p. 135, doi. 10.1007/s11094-013-0911-8
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Synthesis and Anticonvulsive Activity of 7-Amino-Substituted Cyclopenta[4′,5′]-pyrido[3′,2′:4,5]furo[3,2- d]pyrimidines.
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- Pharmaceutical Chemistry Journal, 2013, v. 47, n. 3, p. 130, doi. 10.1007/s11094-013-0910-9
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Synthesis and anticonvulsant activity of condensed thieno[2,3- e]pyrrolo[1,2- a]pyrimidin-8,12-diones.
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- Pharmaceutical Chemistry Journal, 2013, v. 47, n. 2, p. 92, doi. 10.1007/s11094-013-0902-9
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Antagonists of serotonin 5-HT receptors. iv. synthesis and structure-activity interactions in amines containing the 3-(arylsulfonyl)-2-(methylthio)pyrazolo[1,5- a]pyrimidine fragment.
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- Pharmaceutical Chemistry Journal, 2013, v. 46, n. 10, p. 595, doi. 10.1007/s11094-013-0853-1
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