Works matching DE "AZA compounds"
Results: 170
Gold(I)/Copper(II)-Cocatalyzed Tandem Cyclization/Semipinacol Reaction: Construction of 6- Aza/Oxa-Spiro[4.5]decane Skeletons and Formal Synthesis of (±)-Halichlorine.
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- Advanced Synthesis & Catalysis, 2015, v. 357, n. 4, p. 747, doi. 10.1002/adsc.201400932
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Synthesis and Cytotoxic Activity of Aza-Michael Reaction Products from Ethyl Sorbate and Heterocyclic Amines.
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- Chemistry of Natural Compounds, 2015, v. 51, n. 2, p. 296, doi. 10.1007/s10600-015-1264-1
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Activation-free one-pot alkynylation-cyclization synthesis of 2-substituted 4-azaindoles and indoles.
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- Chemistry of Heterocyclic Compounds, 2018, v. 54, n. 3, p. 334, doi. 10.1007/s10593-018-2269-z
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Design of selective COX-2 inhibitors in the (aza)indazole series. Chemistry, in vitro studies, radiochemistry and evaluations in rats of a [<sup>18</sup>F] PET tracer.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2019, v. 34, n. 1, p. 1, doi. 10.1080/14756366.2018.1501043
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Mycophenolic acid and 6-mercaptopurine both inhibit B-cell proliferation in granulomatosis with polyangiitis patients, whereas only mycophenolic acid inhibits B-cell IL-6 production.
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- PLoS ONE, 2020, v. 15, n. 7, p. 1, doi. 10.1371/journal.pone.0235743
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MgO nanoparticles as an efficient and reusable catalyst for aza-Michael reaction.
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- Journal of the Iranian Chemical Society, 2014, v. 11, n. 3, p. 665, doi. 10.1007/s13738-013-0338-x
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Facile Synthesis of Spirocyclic Lactams via [3+2] and [3+3] Aza-Annulation Reactions.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 14, p. 2121, doi. 10.1002/ejoc.202100255
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A Novel Approach to N-Tf 2-Aryl-2,3-Dihydroquinolin-4(1H)-ones via a Ligand-Free Pd(II)-Catalyzed Oxidative Aza-Michael Cyclization.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 4, p. 618, doi. 10.1002/ejoc.202001425
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Endocyclic Enamides Derived from Aza‐Diketopiperazines as Olefin Partners in Povarov Reaction: An Access to Tetracyclic N‐Heterocycles.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 47, p. 7385, doi. 10.1002/ejoc.202001339
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Front Cover: Lewis Acid Catalyzed Intramolecular [4+2] Cycloaddition of In Situ Generated Aza‐Quinone Methides for the Stereoselective Synthesis of Furo/pyrano[3,2‐c]tetrahydroquinolines (Eur. J. Org. Chem. 44/2020).
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 44, p. 6814, doi. 10.1002/ejoc.202001247
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Substrate‐Controlled [5+1] Annulation of 5‐Amino‐1H‐phenylpyrazoles with Alkenes: Divergent Synthesis of Multisubstituted 4,5‐Dihydropyrazolo[1,5‐a]quinazolines.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 26, p. 3997, doi. 10.1002/ejoc.202000536
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- Article
C(sp<sup>3</sup>)‐H Functionalization of 2‐Methyl Azaarenes: Highly Facile Approach to Aza‐Heterocyclic Compounds.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 15, p. 2155, doi. 10.1002/ejoc.201901899
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Linker‐Free Near‐IR Aza‐BODIPY‐Glutamine Conjugates Through Boron Functionalization.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 8, p. 971, doi. 10.1002/ejoc.201901772
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Front Cover: Rearrangement Reactions in Aza‐Vinylogous Povarov Products: Metal‐Free Synthesis of C<sup>3</sup>‐Functionalized Quinolines and Studies on their Synthetic Application (Eur. J. Org. Chem. 38/2019).
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 38, p. 6422, doi. 10.1002/ejoc.201901374
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Rearrangement Reactions in Aza‐Vinylogous Povarov Products: Metal‐Free Synthesis of C<sup>3</sup>‐Functionalized Quinolines and Studies on their Synthetic Application.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 38, p. 6452, doi. 10.1002/ejoc.201900986
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- Article
Tandem Chiral Cu(II) Phosphate‐Catalyzed Deoxygenation of Nitrones/Enantioselective Povarov Reaction with Enecarbamates.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 31/32, p. 5151, doi. 10.1002/ejoc.201900547
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Synthesis of Aza‐Heteroaromatic Dithiocarbamates via Cross‐Coupling Reactions of Aza‐Heteroaromatic Bromides with Tetraalkylthiuram Disulfides.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 18, p. 2941, doi. 10.1002/ejoc.201900475
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Lithium Chloride Catalyzed Asymmetric Domino Aza‐Michael Addition/[3 + 2] Cycloaddition Reactions for the Synthesis of Spiro‐ and Bicyclic α,β,γ‐Triamino Acid Derivatives.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 37, p. 5213, doi. 10.1002/ejoc.201800585
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Bio‐Based Chiral Amines via Aza‐Michael Additions to (–)‐Levoglucosenone Under Aqueous Conditions.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 17, p. 2028, doi. 10.1002/ejoc.201800388
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Structure and Conformational Studies of Aza-Crown 8-Amino-BODIPY Derivatives: Influence of Steric Hindrance on Their Photophysical Properties.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 42, p. 6283, doi. 10.1002/ejoc.201701016
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Selective Synthesis of Hetero-Sequenced Aza-Cyclophanes.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 12, p. 1657, doi. 10.1002/ejoc.201700106
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Investigation into the Chemistry of Highly Substituted [(Aminocyclopropyl)methyl]alkoxyamines (3-Azabicyclo[3.1.0]hexanes).
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 30, p. 6739, doi. 10.1002/ejoc.201500693
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The crystal structure of (4E,11E,31E,38E)-1,4,12,15,18,26,31,39-Octaaza-7,21,24-trihydroxy-penta-cyclo[13·13·13·1<sup>6,10</sup>·1<sup>20,24</sup>·1<sup>33,37</sup>]tetratetraconta-4,6(44),7,9,11,18,20(43),21,23,25,31,33(42),34,36,38-pentadecaene, C<sub>36</sub>H<sub>42</sub>N<sub>8</sub>O<sub>3</sub>
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- Zeitschrift für Kristallographie / New Crystal Structures, 2016, v. 231, n. 1, p. 13, doi. 10.1515/ncrs-2014-9044
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Aza-γ-carbolines and their benzannelated derivatives: methods of synthesis, chemical and biological properties (Review)*.
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- Chemistry of Heterocyclic Compounds, 2012, v. 47, n. 12, p. 1469, doi. 10.1007/s10593-012-0939-9
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Diels–Alder Polar Reactions of Azaheterocycles: A Theoretical and Experimental Study.
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- Organics, 2022, v. 3, n. 2, p. 102, doi. 10.3390/org3020008
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Function of the Metallomicelle from an Aza-Crown Ether Complex with an Acetamide Branch as a Highly Potent Promoter of Phosphate Diester Hydrolytic Cleavage.
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- Journal of Dispersion Science & Technology, 2016, v. 37, n. 8, p. 1170, doi. 10.1080/01932691.2015.1088451
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(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>B Catalyzed One-Pot Synthesis of Benzo[b]Cyclopenta[e][1,4]Oxazin-2(1H)-One and Thiazin-2(1H)-One Derivatives from Furan-2-yl(Phenyl)Methanol and 2-Aminophenol/Thiophenol.
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- Polycyclic Aromatic Compounds, 2023, v. 43, n. 5, p. 4313, doi. 10.1080/10406638.2022.2089173
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Efficient Synthesis of Substituted Aza-Anthraquinones via Michael Addition–Elimination and Intramolecular Cyclization Reactions under Mild Conditions and Their Fluorescent Properties.
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- Polycyclic Aromatic Compounds, 2023, v. 43, n. 4, p. 3557, doi. 10.1080/10406638.2022.2074475
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An Efficient and Transition Metal-Free Base-Promoted Multi-Component Synthesis of Aza-Fused Polysubstituted Pyrido[2′,3′:3,4]Pyrazolo[1,5-a]Pyrimidine Derivatives.
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- Polycyclic Aromatic Compounds, 2020, v. 40, n. 4, p. 1068, doi. 10.1080/10406638.2018.1526808
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Green and Convenient One-Pot Access to Polyfunctionalized Piperidine Scaffolds via Glutamic Acid Catalyzed Knoevenagel- Intramolecular [4+2] aza-Diels-Alder Imin-Based Multi-Component Reaction Under Ambient Temperature.
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- Polycyclic Aromatic Compounds, 2020, v. 40, n. 3, p. 681, doi. 10.1080/10406638.2018.1472111
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Quantitative Analysis of Uncoated Eszopiclone Tablets by Near-Infrared Spectroscopy.
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- Analytical Letters, 2014, v. 47, n. 11, p. 1938, doi. 10.1080/00032719.2014.888726
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- Article
Optimized Ultrasound-Assisted Emulsification-Microextraction Followed by ICP-OES for Simultaneous Determination of Lanthanum and Cerium in Urine and Water Samples.
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- Analytical Letters, 2012, v. 45, n. 11, p. 1426, doi. 10.1080/00032719.2012.675490
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Identification, method development, validation, and characterization of Aza sugars by an ion-chromatography, high-resolution mass spectrometer, and LC-MS/MS.
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- Journal of Analytical Science & Technology, 2018, v. 9, n. 1, p. 1, doi. 10.1186/s40543-018-0138-0
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Synthesis of 4′-alkyl-8-azaspiro[bicyclo[3.2.1]octane-3,2′-morpholin]-5′-ones.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 1, p. 87, doi. 10.1134/S1070428016010164
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Acylation of 1 H-1,2-diazaphenalenes with aliphatic carboxylic acid anhydrides.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 1, p. 131, doi. 10.1134/S1070428016010255
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Base-Controlled Regiospecific Mono-Benzylation/Allylation and Diallylation of 4-Aryl-5-indolyl-1,2,4-triazole-3-thione: Thio-Aza Allyl Rearrangement.
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- Crystals (2073-4352), 2023, v. 13, n. 7, p. 992, doi. 10.3390/cryst13070992
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MICROWAVE ASSISTED CATALYST AND SOLVENT FREE EFFICIENT SYNTHESIS OF QUINOLINE DERIVATIVES BY THREE COMPONENT ONE POT AZA-DIELS-ALDER REACTION STRATEGY.
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- Rasayan Journal of Chemistry, 2021, v. 14, n. 2, p. 887, doi. 10.31788/RJC.2021.1426216
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SYNTHESIS OF 4-CHLORO-PIPERIDINE DERIVATIVES VIA NbCl<sub>5</sub> MEDIATED AZA-PRINS TYPE CYCLIZATION OF EPOXIDES AND HOMOALLYLIC AMINES.
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- Rasayan Journal of Chemistry, 2020, v. 13, n. 1, p. 494, doi. 10.31788/RJC.2020.1315392
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THE INFLUENCE OF AZA-SUBSTITUTION ON THE AROMATICITY OF SUMANENE.
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- Studia Universitatis Babes-Bolyai, Chemia, 2017, v. 62, n. 4,Tom1, p. 105, doi. 10.24193/subbchem.2017.4.09
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- Article
Dual Catalysis in Domino N-Benzylation/Intramolecular C-H Arylation: Regio- and Chemoselective Synthesis of Annelated Nitrogen Heterocycles.
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- European Journal of Organic Chemistry, 2014, v. 2014, n. 25, p. 5469, doi. 10.1002/ejoc.201402395
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Unified Azoline and Azole Syntheses by Optimized Aza-Wittig Chemistry.
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- European Journal of Organic Chemistry, 2013, v. 2013, n. 16, p. 3290, doi. 10.1002/ejoc.201300160
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Ruthenium-catalyzed [2+2] cycloaddition reactions of a 2-oxa-3-azabicyclo[2.2.1]hept-5-ene with unsymmetrical alkynes.
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- Canadian Journal of Chemistry, 2011, v. 89, n. 12, p. 1494, doi. 10.1139/v11-135
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Insecticidal Evaluation and [4+2] Aza-Diels-Alder Synthesis of 3,7-Diaryl-6,7-dihydro-5 H-6-substituted Thiazolo[3,2-a]pyrimidin-5-ones Under Coupled Ultrasonic Irradiation and PTC.
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- Journal of Heterocyclic Chemistry, 2016, v. 53, n. 1, p. 38, doi. 10.1002/jhet.776
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Rapid, Eco-friendly, and.
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- Journal of Heterocyclic Chemistry, 2016, v. 53, n. 1, p. 164, doi. 10.1002/jhet.1811
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DBU Promoted Facile Synthesis of New Thieno[2,3- b]pyridine/quinoline Derivatives and Their Antimicrobial Evaluation.
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- Journal of Heterocyclic Chemistry, 2013, v. 50, p. E131, doi. 10.1002/jhet.1091
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A convenient synthesis of branched-chain nucleoside isothiocyanates via aza-Claisen rearrangement.
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- Nucleosides, Nucleotides & Nucleic Acids, 2021, v. 40, n. 10, p. 943, doi. 10.1080/15257770.2021.1966799
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Cucurbit[7]uril host-guest complexations of aza-, diaza-, and oxa, azaspirocycloalkanes in aqueous solution.
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- Supramolecular Chemistry, 2019, v. 31, n. 3, p. 172, doi. 10.1080/10610278.2018.1562192
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New tetraaza[14]annulene receptors derived from 2,3-diaminonaphthalene: synthesis and crystal structures.
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- Supramolecular Chemistry, 2013, v. 25, n. 5, p. 276, doi. 10.1080/10610278.2013.766736
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Index Abstracts.
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- Supramolecular Chemistry, 2012, v. 24, n. 7, p. i, doi. 10.1080/10610278.2012.709998
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- Article
The advent of macrocyclic chemistry.
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- Supramolecular Chemistry, 2012, v. 24, n. 7, p. 439, doi. 10.1080/10610278.2012.688123
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- Article