Works matching DE "AZIRIDINES"
Results: 321
4-Styrenesulfonyl-(2-methyl)aziridine: The First Bivalent Aziridine-Monomer for Anionic and Radical Polymerization.
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- Macromolecular Chemistry & Physics, 2018, v. 219, n. 1, p. n/a, doi. 10.1002/macp.201700145
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Synthesis and Biological Evaluation of Deoxycyclophellitols as Human Retaining β‐Glucosidase Inhibitors.
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- Chemistry - A European Journal, 2024, v. 30, n. 70, p. 1, doi. 10.1002/chem.202402988
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Accessing Rare α‐Heterocyclic Aziridines via Brønsted Acid‐catalyzed Michael Addition/Annulation: Scope, Limitations, and Mechanism.
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- Chemistry - A European Journal, 2024, v. 30, n. 21, p. 1, doi. 10.1002/chem.202303993
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Electroreductive Cross‐Electrophile Coupling of Aziridines and Aryl Bromides.
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- Chemistry - A European Journal, 2023, v. 29, n. 36, p. 1, doi. 10.1002/chem.202300959
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Enantioselective [3+2] Cycloaddition of Donor‐Acceptor Aziridines and Imines to Construct 2,5‐trans‐Imidazolidines.
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- Chemistry - A European Journal, 2023, v. 29, n. 18, p. 1, doi. 10.1002/chem.202203757
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Protonated Porphyrins: Bifunctional Catalysts for the Metal‐Free Synthesis of N‐Alkyl‐Oxazolidinones.
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- Chemistry - A European Journal, 2023, v. 29, n. 1, p. 1, doi. 10.1002/chem.202202729
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Asymmetric Synthesis of Heterocyclic Chloroamines and Aziridines by Enantioselective Protonation of Catalytically Generated Enamines**.
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- Chemistry - A European Journal, 2022, v. 28, n. 16, p. 1, doi. 10.1002/chem.202200060
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β‐Phenethylamine Synthesis: N‐Pyridinium Aziridines as Latent Dual Electrophiles.
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- Angewandte Chemie, 2024, v. 136, n. 31, p. 1, doi. 10.1002/ange.202406335
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Chiral Cp<sup>x</sup>Rhodium(III)‐Catalyzed Enantioselective Aziridination of Unactivated Terminal Alkenes.
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- Angewandte Chemie, 2024, v. 136, n. 12, p. 1, doi. 10.1002/ange.202400502
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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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Step‐growth Polymerization of Aziridines with Elemental Sulfur: Easy Access to Linear Polysulfides and Their Use as Recyclable Adhesives.
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- Angewandte Chemie, 2024, v. 136, n. 8, p. 1, doi. 10.1002/ange.202318919
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Divergent Synthesis of Chelating Aziridines and Cyclic(Alkyl)(Amino)Carbenes (CAACs) from Pyridyl‐Tethered Robust Azomethine Ylides.
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- Angewandte Chemie, 2023, v. 135, n. 47, p. 1, doi. 10.1002/ange.202312858
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Frontispiz: Palladium‐Catalyzed Fluorinative Bifunctionalization of Aziridines and Azetidines with gem‐Difluorocyclopropanes.
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- Angewandte Chemie, 2023, v. 135, n. 42, p. 1, doi. 10.1002/ange.202384262
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Palladium‐Catalyzed Fluorinative Bifunctionalization of Aziridines and Azetidines with gem‐Difluorocyclopropanes.
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- Angewandte Chemie, 2023, v. 135, n. 42, p. 1, doi. 10.1002/ange.202310283
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Elucidation of the Alternating Copolymerization Mechanism of Epoxides or Aziridines with Cyclic Anhydrides in the Presence of Halide Salts.
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- Angewandte Chemie, 2023, v. 135, n. 14, p. 1, doi. 10.1002/ange.202218891
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A Modular Approach for Diversity‐Oriented Synthesis of 1,3‐trans‐Disubstituted Tetrahydroisoquinolines: Seven‐Step Asymmetric Synthesis of Michellamines B and C.
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- Angewandte Chemie, 2022, v. 134, n. 31, p. 1, doi. 10.1002/ange.202205245
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Mechanical Force for the Transformation of Aziridine into Imine.
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- Angewandte Chemie, 2021, v. 133, n. 44, p. 23756, doi. 10.1002/ange.202109358
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Well‐Defined Poly(Ester Amide)‐Based Homo‐ and Block Copolymers by One‐Pot Organocatalytic Anionic Ring‐Opening Copolymerization of N‐Sulfonyl Aziridines and Cyclic Anhydrides.
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- Angewandte Chemie, 2021, v. 133, n. 13, p. 7025, doi. 10.1002/ange.202015339
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Kinetic Resolution of Aziridines Enabled by N‐Heterocyclic Carbene/Copper Cooperative Catalysis: Carbene Dose‐Controlled Chemo‐Switchability.
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- Angewandte Chemie, 2021, v. 133, n. 6, p. 3305, doi. 10.1002/ange.202013679
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Halogen‐Imparted Reactivity in Lithium Carbenoid Mediated Homologations of Imine Surrogates: Direct Assembly of bis‐Trifluoromethyl‐β‐Diketiminates and the Dual Role of LiCH<sub>2</sub>I.
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- Angewandte Chemie, 2020, v. 132, n. 47, p. 21038, doi. 10.1002/ange.202007954
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Mechanical Force Induces Ylide‐Free Cycloaddition of Nonscissible Aziridines.
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- Angewandte Chemie, 2020, v. 132, n. 12, p. 4913, doi. 10.1002/ange.201915438
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Highly Enantioselective Synthesis of Fused Tri‐ and Tetrasubstituted Aziridines: aza‐Darzens Reaction of Cyclic Imines with α‐Halogenated Ketones Catalyzed by Bifunctional Phosphonium Salt.
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- Angewandte Chemie, 2019, v. 131, n. 22, p. 7503, doi. 10.1002/ange.201900613
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Telescoped, Divergent, Chemoselective C1 and C1‐C1 Homologation of Imine Surrogates: Access to Quaternary Chloro‐ and Halomethyl‐Trifluoromethyl Aziridines.
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- Angewandte Chemie, 2019, v. 131, n. 8, p. 2501, doi. 10.1002/ange.201812525
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An outer shell of positively charged poly(ethyleneimine) strongly increases the transfection efficiency of calcium phosphate/DNA nanoparticles.
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- Journal of Materials Science, 2010, v. 45, n. 18, p. 4952, doi. 10.1007/s10853-009-4159-3
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DFT Study on the Molecular Mechanism, Thermodynamic and Kinetic Parameters of Cycloaddition Reaction of Aziridine with CO<sub>2</sub> in the Presence of Organocatalysts (TBD and 7-Azaindole).
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- Trends in Sciences, 2023, v. 20, n. 3, p. 1, doi. 10.48048/tis.2023.6520
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A novel matrix metalloproteinase-2 inhibitor triazolylmethyl aziridine reduces melanoma cell invasion, angiogenesis and targets ERK1/2 phosphorylation.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2014, v. 29, n. 6, p. 765, doi. 10.3109/14756366.2013.855207
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Efficient Asymmetric Simmons-Smith Cyclopropanation and Diethylzinc Addition to Aldehydes Promoted by Enantiomeric Aziridine-Phosphines.
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- Catalysts (2073-4344), 2021, v. 11, n. 8, p. 968, doi. 10.3390/catal11080968
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Asymmetric Friedel–Crafts Alkylation of Indoles Catalyzed by Chiral Aziridine-Phosphines.
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- Catalysts (2073-4344), 2020, v. 10, n. 9, p. 971, doi. 10.3390/catal10090971
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Enantioselective Mannich Reaction Promoted by Chiral Phosphinoyl-Aziridines.
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- Catalysts (2073-4344), 2019, v. 9, n. 10, p. 837, doi. 10.3390/catal9100837
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Aziridine- and Azetidine-Pd Catalytic Combinations. Synthesis and Evaluation of the Ligand Ring Size Impact on Suzuki-Miyaura Reaction Issues.
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- Catalysts (2073-4344), 2017, v. 7, n. 1, p. 27, doi. 10.3390/catal7010027
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Chiral Aziridine Phosphines as Highly Effective Promoters of Asymmetric Rauhut–Currier Reaction.
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- Symmetry (20738994), 2022, v. 14, n. 8, p. 1631, doi. 10.3390/sym14081631
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2-AIZVIETOTU AZIRIDĪNU N-VINILĒŠANA AR MALONSKĀBES ATVASINĀJUMIEM.
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- Material Science & Applied Chemistry, 2009, n. 20, p. 141
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DEVELOPMENT OF STANDARD PROTOCOLS FOR PREPARATION AND EVALUATION OF LIVER HOMOGENATE VACCINES AGAINST HYDROPERIC ARDIUM SYNDROME VIRUS IN POULTRY.
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- Pakistan Veterinary Journal, 2008, v. 28, n. 4, p. 163
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Three-membered ring amides - a calculational and conceptual study of the structure and energetics of 1,2-oxaziridine-3-one and aziridine-2,3-dione.
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- Canadian Journal of Chemistry, 2015, v. 93, n. 4, p. 406, doi. 10.1139/cjc-2014-0321
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AGOA hydration clusters produce the solvation effect on the aziridine···hydrofluoric acid complex — A modern proposal.
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- Canadian Journal of Chemistry, 2010, v. 88, n. 4, p. 338, doi. 10.1139/V10-012
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Synthesis of both isomers of aziridine derived from the mixture of cis- and trans-limonene oxide.
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- Canadian Journal of Chemistry, 2009, v. 87, n. 8, p. 1117, doi. 10.1139/V09-085
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A DFT investigation into the origin of regioselectivity in palladium-catalyzed allylic amination.
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- Canadian Journal of Chemistry, 2009, v. 87, n. 1, p. 54, doi. 10.1139/V08-078
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Photolytic aziridination by thianthrene sulfilimine derivatives.
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- Journal of Sulfur Chemistry, 2008, v. 29, n. 5, p. 459, doi. 10.1080/17415990802183868
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A rapid and efficient polyethylenimine-based transfection method to prepare lentiviral or retroviral vectors: useful for making iPS cells and transduction of primary cells.
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- Biotechnology Letters, 2016, v. 38, n. 9, p. 1631, doi. 10.1007/s10529-016-2123-2
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Highly enantioselective asymmetric direct aldol reaction promoted by aziridine amides constructed on chiral terpene scaffold.
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- Chirality, 2017, v. 29, n. 5, p. 213, doi. 10.1002/chir.22698
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Enantioselective Preparation, Conformational Analysis and Absolute Configuration of Highly Substituted Aziridines†.
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- Chirality, 2015, v. 27, n. 12, p. 875, doi. 10.1002/chir.22522
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Organic synthesis using carbon dioxide as phosgene-free carbonyl reagent.
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- Pure & Applied Chemistry, 2012, v. 84, n. 3, p. 581
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Copper-catalyzed enantioselective aziridination of styrenes.
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- Pure & Applied Chemistry, 2010, v. 82, n. 9, p. 1827, doi. 10.1351/PAC-CON-09-12-12
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Use of functionalized β-lactams as building blocks in heterocyclic chemistry.
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- Pure & Applied Chemistry, 2010, v. 82, n. 9, p. 1749, doi. 10.1351/PAC-CON-09-09-39
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Mechanism studies of the chemoselective ring opening of N-tosyl aziridines with aldehydes catalyzed by an N-heterocyclic carbene under aerobic conditions.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2016, v. 135, n. 3, p. 1, doi. 10.1007/s00214-016-1820-1
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Recent Developments in Stereoselective Reactions of Sulfonium Ylides.
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- Organics, 2022, v. 3, n. 3, p. 320, doi. 10.3390/org3030024
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New vibrational assignments for the ν 1 to ν 17 vibrational modes of aziridine and first analysis of the high-resolution infrared spectrum of aziridine between 720 and 1050 cm.
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- Molecular Physics, 2011, v. 109, n. 17/18, p. 2153, doi. 10.1080/00268976.2011.605774
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Aminopyridinium iodide as a NH transferring agent for the synthesis of 2-aroyl-3-aryl aziridines.
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- Journal of the Iranian Chemical Society, 2015, v. 12, n. 12, p. 2221, doi. 10.1007/s13738-015-0700-2
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Deamination of cis and trans-aziridines using diethyl thiourea and iodine.
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- Journal of the Iranian Chemical Society, 2012, v. 9, n. 5, p. 705, doi. 10.1007/s13738-012-0094-3
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Stereoselective ( exo-specific) synthesis, dynamic H NMR and quantum chemical conformational and configurational analysis of norbornene-aziridine- E-imidoyl system.
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- Journal of the Iranian Chemical Society, 2012, v. 9, n. 3, p. 339, doi. 10.1007/s13738-011-0029-4
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