Works matching DE "AZIRIDINATION"
Results: 167
Stable CAAC‐Triazenes: A New Nitrogen Ligand System With Donor and Conformational Flexibility, and With Application in Olefin Activation Catalysis.
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- Chemistry - A European Journal, 2024, v. 30, n. 38, p. 1, doi. 10.1002/chem.202400400
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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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Copper‐Catalyzed Heterocyclic Recombination of Aziridine and Diazetidine for the Synthesis of Imidazolidine.
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- Chemistry - A European Journal, 2023, v. 29, n. 43, p. 1, doi. 10.1002/chem.202301071
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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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Organo‐Photocatalytic Anti‐Markovnikov Hydroamidation of Alkenes with Sulfonyl Azides: A Combined Experimental and Computational Study.
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- Angewandte Chemie, 2024, v. 136, n. 26, p. 1, doi. 10.1002/ange.202406069
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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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Photocatalytic Generation of Trifluoromethyl Nitrene for Alkene Aziridination.
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- Angewandte Chemie, 2024, v. 136, n. 2, p. 1, doi. 10.1002/ange.202315162
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Sulfenate Anion Catalyzed Diastereoselective Synthesis of Aziridines.
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- Angewandte Chemie, 2023, v. 135, n. 25, p. 1, doi. 10.1002/ange.202303069
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A Stereospecific Alkene 1,2‐Aminofunctionalization Platform for the Assembly of Complex Nitrogen‐Containing Ring Systems.
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- Angewandte Chemie, 2023, v. 135, n. 16, p. 1, doi. 10.1002/ange.202301262
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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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Strain‐Release Driven Epoxidation and Aziridination of Bicyclo[1.1.0]butanes via Palladium Catalyzed σ‐Bond Nucleopalladation.
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- Angewandte Chemie, 2023, v. 135, n. 7, p. 1, doi. 10.1002/ange.202217064
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Intermolecular Metal‐Free Cyclopropanation and Aziridination of Alkenes with XH<sub>2</sub> (X=N, C) by Thianthrenation**.
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- Angewandte Chemie, 2022, v. 134, n. 41, p. 1, doi. 10.1002/ange.202209929
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Lipid Mass Tags via Aziridination for Probing Unsaturated Lipid Isomers and Accurate Relative Quantification**.
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- Angewandte Chemie, 2022, v. 134, n. 39, p. 1, doi. 10.1002/ange.202207098
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Sterically Demanding Flexible Phosphoric Acids for Constructing Efficient and Multi‐Purpose Asymmetric Organocatalysts.
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- Angewandte Chemie, 2022, v. 134, n. 26, p. 1, doi. 10.1002/ange.202202189
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Nitrene Photochemistry of Manganese N‐Haloamides**.
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- Angewandte Chemie, 2021, v. 133, n. 51, p. 26851, doi. 10.1002/ange.202108304
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Copper‐Nitrene‐Catalyzed Desymmetric Oxaziridination/1,2‐Alkyl Rearrangement of 1,3‐Diketones toward Bicyclic Lactams.
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- Angewandte Chemie, 2021, v. 133, n. 42, p. 22870, doi. 10.1002/ange.202107909
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Aromatic sulphonamides of aziridine-2-carboxylic acid derivatives as novel PDIA1 and PDIA3 inhibitors.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2023, v. 38, n. 1, p. 1, doi. 10.1080/14756366.2022.2158187
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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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Mechanism and Chemoselectivity of Mn-Catalyzed Intramolecular Nitrene Transfer Reaction: C–H Amination vs. C=C Aziridination.
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- Catalysts (2073-4344), 2020, v. 10, n. 3, p. 292, doi. 10.3390/catal10030292
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Bach Goes to Town †.
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- Biomolecules (2218-273X), 2018, v. 8, n. 3, p. 75, doi. 10.3390/biom8030075
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A Mechanistic Study for Aziridination of Nitroalkenes Mediated by N-Chlorosuccinimide.
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- Journal of Oleo Science, 2022, v. 71, n. 6, p. 897, doi. 10.5650/jos.ess21406
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An Aza‐Prilezhaev‐Based Method for Inversion of Regioselectivity in Stereospecific Alkene 1,2‐Aminohydroxylations.
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- Angewandte Chemie, 2024, v. 136, n. 49, p. 1, doi. 10.1002/ange.202409836
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Step economy strategy for the synthesis of amphoteric aminoaldehydes, key intermediates for reduced hydantoins.
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- Pure & Applied Chemistry, 2018, v. 90, n. 1, p. 121, doi. 10.1515/pac-2017-0705
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Efficient Regioselective Ring Opening of Activated Aziridine-2-Carboxylates with [<sup>18</sup>F]Fluoride.
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- ChemistryOpen, 2015, v. 4, n. 1, p. 65, doi. 10.1002/open.201402081
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Fe(NO) as an efficient catalyst for regio- and stereo-controlled ring expansion of 1,2-diaroyl-3-arylaziridines.
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- Journal of the Iranian Chemical Society, 2014, v. 11, n. 4, p. 979, doi. 10.1007/s13738-013-0364-8
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Nanocrystalline magnesium oxide as a solid base catalyst promoted one pot synthesis of gem-dichloroaziridine derivatives under thermal conditions.
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- Journal of the Iranian Chemical Society, 2013, v. 10, n. 1, p. 161, doi. 10.1007/s13738-012-0137-9
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Electrochemical flow aziridination of unactivated alkenes.
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- National Science Review, 2023, v. 10, n. 10, p. 1, doi. 10.1093/nsr/nwad187
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Copper‐Catalyzed Oxidative Trifluoromethylation of Aromatic Alkenes for the Synthesis of α‐Trifluoromethylated Ketones.
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- Asian Journal of Organic Chemistry, 2024, v. 13, n. 3, p. 1, doi. 10.1002/ajoc.202300638
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Visible Light Photoredox Aziridination of Chalcones.
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- Asian Journal of Organic Chemistry, 2023, v. 12, n. 11, p. 1, doi. 10.1002/ajoc.202300415
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Front Cover: Highly Efficient and Stereoselective Mukaiyama Aldol Reaction with Chiral Aziridine‐2‐carboxaldehyde and Its Synthetic Applications (Asian J. Org. Chem. 1/2022).
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- Asian Journal of Organic Chemistry, 2022, v. 11, n. 1, p. 1, doi. 10.1002/ajoc.202100712
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Asymmetric Organocatalytic Aziridination: Recent Advances.
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- Asian Journal of Organic Chemistry, 2018, v. 7, n. 12, p. 2357, doi. 10.1002/ajoc.201800431
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Unprotected Aziridines: A Synthetic Overview.
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- Asian Journal of Organic Chemistry, 2017, v. 6, n. 7, p. 782, doi. 10.1002/ajoc.201700056
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Highly Efficient Asymmetric Morita–Baylis–Hillman Reaction Promoted by Chiral Aziridine-Phosphines.
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- Catalysts (2073-4344), 2022, v. 12, n. 4, p. 394, doi. 10.3390/catal12040394
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N-Aminopyridinium reagents as traceless activating groups in the synthesis of N-Aryl aziridines.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-31032-w
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Copper(I)‐Photocatalyzed Diastereoselective Aziridination of N‐Sulfonyl Imines with Vinyl Azides: Application to Benzo[f][1,2,3]oxathiazepines Dioxides and Fused Isoxazolines.
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- Chemistry - An Asian Journal, 2024, v. 19, n. 2, p. 1, doi. 10.1002/asia.202300904
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Catalyst‐ and Additive‐Free Methodical Ring Expansion Protocol to Access Benzooxepino‐Fused Pyrroles.
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- Chemistry - An Asian Journal, 2023, v. 18, n. 4, p. 1, doi. 10.1002/asia.202201071
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Bi(OTf)<sub>3</sub>‐catalyed One‐pot Synthesis of α‐Halo‐β‐amino Ketones and Acyl Aziridines from 3‐Aryl Propargyl Alcohols.
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- Chemistry - An Asian Journal, 2021, v. 16, n. 13, p. 1832, doi. 10.1002/asia.202100368
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Efficient Synthesis of Aza-triquinacene Derivatives via Cycloaddition of 2,6-Diazasemibullvalenes with Nitroso Compounds.
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- Chemistry - An Asian Journal, 2015, v. 10, n. 4, p. 862, doi. 10.1002/asia.201403030
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Aziridination and aza-Wharton Reactions of Levoglucosenone.
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- Australian Journal of Chemistry, 2019, v. 72, n. 5, p. 362, doi. 10.1071/CH18574
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Brønsted Base-Mediated Aziridination of 2-Alkyl-Substituted-1,3-Dicarbonyl Compounds and 2-Acyl-Substituted-1,4-Dicarbonyl Compounds by Iminoiodanes.
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- Australian Journal of Chemistry, 2017, v. 70, n. 4, p. 430, doi. 10.1071/CH16580
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Aziridination Exploited: A Mechanistic Study of the Divergent Reactivity of Trifluoropropenyl‐iodonium Reagent toward N‐nucleophiles.
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- European Journal of Organic Chemistry, 2024, v. 27, n. 45, p. 1, doi. 10.1002/ejoc.202400779
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A New Strategy for the Synthesis of (+)‐Crambescin B Decarboxylate.
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- European Journal of Organic Chemistry, 2024, v. 27, n. 19, p. 1, doi. 10.1002/ejoc.202400176
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N‐Boc‐Protected α‐Amino Acids by 1,3‐Migratory Nitrene C(sp<sup>3</sup>)−H Insertion.
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- European Journal of Organic Chemistry, 2023, v. 26, n. 26, p. 1, doi. 10.1002/ejoc.202300296
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A One‐Pot Approach to Multi‐Substituted Fused Aziridines: Formal Intermolecular [2+1] Cycloaddition Reaction between Saccharin‐Derived Cyclic Ketimines and Sulfur Ylides.
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- European Journal of Organic Chemistry, 2023, v. 26, n. 25, p. 1, doi. 10.1002/ejoc.202300300
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Fluorinated alcohols: powerful promoters for ring-opening reactions of epoxides with carbon nucleophiles.
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- ARKIVOC: Online Journal of Organic Chemistry, 2021, v. 2021, p. 85, doi. 10.24820/ark.5550190.p011.449
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Synthesis of chiral 1-(2-aminoalkyl)aziridines via a self-opening reaction of aziridine.
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- ARKIVOC: Online Journal of Organic Chemistry, 2017, v. 2017, p. 223, doi. 10.3998/ark.5550190.p009.741
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Efficient fixation of CO<sub>2</sub> to cyclic carbonates and oxazolidinones with multi-hydroxyl bis-(quaternary ammonium) ionic liquids as catalysts under mild conditions.
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- Journal of South-Central Minzu University (Natural Science Edition), 2025, v. 44, n. 1, p. 1, doi. 10.20056/j.cnki.ZNMDZK.20250742
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Telescoped synthesis of vicinal diamines via ring-opening of electrochemically generated aziridines in flow.
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- Journal of Flow Chemistry, 2024, v. 14, n. 1, p. 139, doi. 10.1007/s41981-023-00296-8
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A continuous flow bromodimethylsulfonium bromide generator: application to the synthesis of 2-arylaziridines from styrenes.
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- Journal of Flow Chemistry, 2021, v. 11, n. 2, p. 117, doi. 10.1007/s41981-020-00125-2
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Transition‐Metal Catalyzed Enantioselective Aziridination Reaction: Recent Development in Catalysis and Future Perspectives.
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- ChemCatChem, 2024, v. 16, n. 21, p. 1, doi. 10.1002/cctc.202400791
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