Works about AZETIDINE
Results: 118
Synthesis and Functionalization of Azetidine‐Containing Small Macrocyclic Peptides.
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- Chemistry - A European Journal, 2024, v. 30, n. 28, p. 1, doi. 10.1002/chem.202400308
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Mono‐ and Difluorinated Saturated Heterocyclic Amines for Drug Discovery: Systematic Study of Their Physicochemical Properties.
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- Chemistry - A European Journal, 2023, v. 29, n. 47, p. 1, doi. 10.1002/chem.202301383
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Cover Feature: Substituent and Solvent Effect Studies of N‐Alkenylnitrone 4π Electrocyclizations (Chem. Eur. J. 30/2023).
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- Chemistry - A European Journal, 2023, v. 29, n. 30, p. 1, doi. 10.1002/chem.202301211
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Substituent and Solvent Effect Studies of N‐Alkenylnitrone 4π Electrocyclizations.
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- Chemistry - A European Journal, 2023, v. 29, n. 30, p. 1, doi. 10.1002/chem.202300551
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Azetidines‐Containing Fluorescent Purine Analogs: Synthesis and Photophysical Properties.
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- Chemistry - A European Journal, 2022, v. 28, n. 30, p. 1, doi. 10.1002/chem.202200765
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- Article
Rhodium‐Catalyzed One‐Carbon Ring Expansion of Aziridines with Vinyl‐N‐triftosylhydrazones for the Synthesis of 2‐Vinyl Azetidines.
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- Angewandte Chemie, 2024, v. 136, n. 12, p. 1, doi. 10.1002/ange.202318072
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Photosensitized [4+2]‐ and [2+2]‐Cycloaddition Reactions of N‐Sulfonylimines.
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- Angewandte Chemie, 2023, v. 135, n. 32, p. 1, doi. 10.1002/ange.202305622
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Inherently Emissive Puromycin Analogues for Live Cell Labelling.
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- Angewandte Chemie, 2023, v. 135, n. 23, p. 1, doi. 10.1002/ange.202216784
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Umpolung Asymmetric 1,5‐Conjugate Addition via Palladium Hydride Catalysis.
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- Angewandte Chemie, 2023, v. 135, n. 2, p. 1, doi. 10.1002/ange.202215568
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Four‐Component Strain‐Release‐Driven Synthesis of Functionalized Azetidines.
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- Angewandte Chemie, 2022, v. 134, n. 52, p. 1, doi. 10.1002/ange.202214049
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Arene Activation through Iminium Ions: Product Diversity from Intramolecular Photocycloaddition Reactions.
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- Angewandte Chemie, 2022, v. 134, n. 40, p. 1, doi. 10.1002/ange.202208329
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Asymmetric Auto‐Tandem Palladium Catalysis for 2,4‐Dienyl Carbonates: Ligand‐Controlled Divergent Synthesis.
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- Angewandte Chemie, 2022, v. 134, n. 17, p. 1, doi. 10.1002/ange.202200880
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Strain‐Release‐Driven Friedel–Crafts Spirocyclization of Azabicyclo[1.1.0]butanes.
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- Angewandte Chemie, 2022, v. 134, n. 3, p. 1, doi. 10.1002/ange.202114235
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Divergent, Strain‐Release Reactions of Azabicyclo[1.1.0]butyl Carbinols: Semipinacol or Spiroepoxy Azetidine Formation.
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- Angewandte Chemie, 2021, v. 133, n. 13, p. 7436, doi. 10.1002/ange.202100583
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Synthesis of Eight‐Membered Lactams through Formal [6+2] Cyclization of Siloxy Alkynes and Vinylazetidines.
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- Angewandte Chemie, 2019, v. 131, n. 20, p. 6848, doi. 10.1002/ange.201902866
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Azetidine‐Containing Alkaloids Produced by a Quorum‐Sensing Regulated Nonribosomal Peptide Synthetase Pathway in Pseudomonas aeruginosa.
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- Angewandte Chemie, 2019, v. 131, n. 10, p. 3210, doi. 10.1002/ange.201809981
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Molecular structure, quantum chemical investigation, and thermal behavior of (DNAZ-CO).
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- Journal of Structural Chemistry, 2012, v. 53, n. 3, p. 534, doi. 10.1134/S0022476612030171
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Synthesis, Identification and Assess the Biological and Laser Efficacy of New Compounds of Azetidine Derived from Benzidine.
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- AL-Muthanna Journal of Pure Science, 2020, v. 7, n. 2, p. 12, doi. 10.52113/2/07.02.2020/12-25
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Ionic liquid mediated synthesis, reactions, and insecticidal activity of 1-[(1H-benzoimidazol-2-yl)amino]spiro[azetidine-4,4'-[4'H]chroman]-2-ones.
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- Turkish Journal of Chemistry, 2013, v. 37, n. 2, p. 239, doi. 10.3906/kim-1206-47
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( S)-1-(Pent-4′-enoyl)-4-(hydroxymethyl)-azetidin-2-one derivatives as inhibitors of human fatty acid amide hydrolase ( hFAAH): synthesis, biological evaluation and molecular modelling.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2014, v. 29, n. 5, p. 654, doi. 10.3109/14756366.2013.837900
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The roles of Arabidopsis HSFA2, HSFA4a, and HSFA7a in the heat shock response and cytosolic protein response.
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- Botanical Studies, 2018, v. 59, n. 1, p. 1, doi. 10.1186/s40529-018-0231-0
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Regio‐ and Diastereoselective Synthesis of Polysubstituted Piperidines Enabled by Boronyl Radical‐Catalyzed (4+2) Cycloaddition.
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- Angewandte Chemie, 2024, v. 136, n. 38, p. 1, doi. 10.1002/ange.202406612
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Exploiting structural and conformational effects for a site-selective lithiation of azetidines.
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- Pure & Applied Chemistry, 2016, v. 88, n. 7, p. 631, doi. 10.1515/pac-2016-0602
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In this issue.
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- Pure & Applied Chemistry, 2016, v. 88, n. 7, p. iv, doi. 10.1515/pac-2016-graphabs7
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Strain and Complexity, Passerini and Ugi Reactions of Four‐Membered Heterocycles and Further Elaboration of TOSMIC Product.
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- ChemistryOpen, 2023, v. 12, n. 8, p. 1, doi. 10.1002/open.202200083
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Structurally Divergent Synthesis of Azetidines, 5,6‐Dihydro‐1,3‐oxazines and 2,3‐Dihydro‐1,4‐oxazines through Palladium‐Catalyzed Tandem Allylic Substitution Reaction.
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- Chinese Journal of Chemistry, 2024, v. 42, n. 22, p. 2773, doi. 10.1002/cjoc.202400533
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Synthesis of Diverse Oxetane Amino Acids via Visible‐Light‐Induced Photocatalytic Decarboxylative Giese‐Type Reaction.
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- Chinese Journal of Chemistry, 2024, v. 42, n. 12, p. 1341, doi. 10.1002/cjoc.202300750
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BF<sub>3</sub>·OEt<sub>2</sub> catalyzed base-free regiospecific ring opening of N-activated azetidines with (E)-1-arylidene-2-arylhydrazines.
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- Journal of the Iranian Chemical Society, 2019, v. 16, n. 1, p. 127, doi. 10.1007/s13738-018-1489-6
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Synthesis and Applications of 3-Methylene-4- (trifluoromethyl)azetidin-2-ones as Building Blocks for the Preparation of Mono- and Spirocyclic 4-CF<sub>3</sub>-β-Lactams.
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- Asian Journal of Organic Chemistry, 2016, v. 5, n. 12, p. 1480, doi. 10.1002/ajoc.201600387
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Bicyclic azetidines target acute and chronic stages of Toxoplasma gondii by inhibiting parasite phenylalanyl t-RNA synthetase.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-28108-y
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Front Cover: Forging C−S Bonds on the Azetidine Ring by Continuous Flow Photochemical Addition of Thiols and Disulfides to Azetines (Eur. J. Org. Chem. 33/2023).
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- European Journal of Organic Chemistry, 2023, v. 26, n. 33, p. 1, doi. 10.1002/ejoc.202300849
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Forging C−S Bonds on the Azetidine Ring by Continuous Flow Photochemical Addition of Thiols and Disulfides to Azetines.
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- European Journal of Organic Chemistry, 2023, v. 26, n. 33, p. 1, doi. 10.1002/ejoc.202300413
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3-Aminopropylazetidines: facile synthesis and application for medicinal chemical purposes.
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- ARKIVOC: Online Journal of Organic Chemistry, 2022, v. 2022, p. 1, doi. 10.24820/ark.5550190.p011.900
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A simple and general synthetic route to N-alkylazetidines from 1,2-amino alcohols.
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- ARKIVOC: Online Journal of Organic Chemistry, 2022, v. 2022, p. 87, doi. 10.24820/ark.5550190.p011.727
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Synthesis of 3-fluoropyrrolidines and 3-fluoroazetidines.
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- ARKIVOC: Online Journal of Organic Chemistry, 2012, p. 6
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Thermal Behaviour and Detonation Characterization of N-Benzoyl-3,3-dinitroazetidine.
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- South African Journal of Chemistry, 2013, v. 66, p. 136
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Synthetic aspects and Biological Studies of some Heterocycles.
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- Chemistry & Biology Interface, 2017, v. 7, n. 2, p. 79
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Pyrolysis Products from Osmanthus Fragrans Wood.
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- Ekoloji Dergisi, 2019, n. 108, p. 105
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Nitro derivatives of triazetidine: potential high energy density materials.
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- Journal of Molecular Modeling, 2018, v. 24, n. 8, p. 1, doi. 10.1007/s00894-018-3733-5
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Theoretical study of the ring expansion reaction mechanism of cyclopropenylidene with azetidine.
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- Journal of Molecular Modeling, 2014, v. 20, n. 3, p. 1, doi. 10.1007/s00894-014-2088-9
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Lewis Acid‐Mediated Ring Contraction of 2,4‐Diaryl‐2,3‐dihydro‐1H‐1,5‐benzodiazepines: Access to 2‐Aryl‐1‐styrylbenzimidazoles.
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- Helvetica Chimica Acta, 2023, v. 106, n. 4, p. 1, doi. 10.1002/hlca.202200143
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Computational Study of Benzosultam Formation through Gold(I)‐Catalyzed Ammoniumation/Nucleophilic Substitution Reaction.
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- Helvetica Chimica Acta, 2021, v. 104, n. 10, p. 1, doi. 10.1002/hlca.202100133
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An efficient synthesis of baricitinib.
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- Journal of Chemical Research, 2016, v. 40, n. 4, p. 205, doi. 10.3184/174751916X14569294811333
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2-Arylazetidines as ligands for nicotinic acetylcholine receptors.
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 3, p. 329, doi. 10.1007/s10593-017-2061-5
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Synthesis and Characterization of 3,3'-(disulfanediylbis (methylene)) bis(1,4-bis(4-bromophenyl)azetidin-2-one).
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- International Journal of Pharmaceutical Research (09752366), 2020, v. 12, n. 2, p. 1845, doi. 10.31838/ijpr/2020.12.02.193
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Synthesis, Characterization and Biological Evaluation of Azetidine Analogues and Related Compounds.
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- International Journal of Pharmaceutical Research (09752366), 2020, v. 12, n. 2, p. 2040, doi. 10.31838/ijpr/2020.12.02.274
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Synthesis and in-vitro Antioxidant Activity of Novel Schiff Bases and Azetidines Derived from Phenyl Urea Derivatives.
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- Indian Journal of Pharmaceutical Education & Research, 2017, v. 51, p. S707, doi. 10.5530/ijper.51.4s.102
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ASSESSMENT OF IN VITRO ANTIOXIDANT AND ANTIINFLAMMATORY ACTIVITIES OF NEW AZETIDIN-2-ONE DERIVATIVES OF FERULIC ACID.
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- Farmacia, 2016, v. 64, n. 5, p. 717
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A Computational Study of Reaction Routes of 1,3,3-trinitroazetidine (TNAZ) Synthesis.
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- Journal of the Chinese Chemical Society, 2015, v. 62, n. 9, p. 803, doi. 10.1002/jccs.201500187
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Front Cover: Fluorine‐Containing sp<sup>3</sup>‐Enriched Building Blocks for the Multigram Synthesis of Fluorinated Pyrazoles and Pyrimidines with (Hetero)aliphatic Substituents (Eur. J. Org. Chem. 15/2022).
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- European Journal of Organic Chemistry, 2022, v. 2022, n. 15, p. 1, doi. 10.1002/ejoc.202200274
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