Works matching DE "CYCLOPROPANE derivatives"
Results: 118
Breaking the Rules: On the Relative Stability of Some Methylencyclopropane and Methylcyclopropene Derivatives.
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- Chemistry - A European Journal, 2024, v. 30, n. 29, p. 1, doi. 10.1002/chem.202400431
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Photochemical Synthesis of Lactones, Cyclopropanes and ATRA Products: Revealing the Role of Sodium Ascorbate**.
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- Chemistry - A European Journal, 2024, v. 30, n. 21, p. 1, doi. 10.1002/chem.202400253
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Synthesis of Trifluoromethylated Monoterpenes by an Engineered Cytochrome P450.
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- Chemistry - A European Journal, 2024, v. 30, n. 10, p. 1, doi. 10.1002/chem.202302936
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Experimental and Computational Studies for the Synthesis of Functionalized Cyclopropanes from 2‐Substituted Allylic Derivatives with Ethyl Diazoacetate.
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- Chemistry - A European Journal, 2024, v. 30, n. 8, p. 1, doi. 10.1002/chem.202303070
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A Widely Applicable and Versatile Method for the Ring‐Opening 1,3‐Carbocarbonation of Donor‐Acceptor Cyclopropanes.
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- Chemistry - A European Journal, 2023, v. 29, n. 20, p. 1, doi. 10.1002/chem.202203986
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Divergent Copper‐salt‐controlled Reactions of Donor‐Acceptor Cyclopropanes and N‐Fluorobenzene Sulfonimide: Access to the 1,3‐Haloamines and Aminoindanes.
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- Chemistry - A European Journal, 2023, v. 29, n. 3, p. 1, doi. 10.1002/chem.202202544
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Divergent Reactivity of D-A Cyclopropanes under PTC Conditions, Ring-Opening vs. Decyanation Reaction.
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- Catalysts (2073-4344), 2023, v. 13, n. 4, p. 760, doi. 10.3390/catal13040760
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SYNTHESIS OF 1,1,2-TRISUBSTITUTED CYCLOPROPANE RING THROUGH CARBON-CARBON BOND NUCLEOPHILE-INTERCEPTED BECKMANN FRAGMENTATION REACTION.
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- Rasayan Journal of Chemistry, 2020, v. 13, n. 4, p. 2352, doi. 10.31788/RJC.2020.1345745
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Potent biological investigation into a new class of sulfone derivatives endowed with quinolinyl–cyclopropane analogue.
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- Journal of the Iranian Chemical Society, 2022, v. 19, n. 5, p. 1613, doi. 10.1007/s13738-021-02402-w
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Synthesis and Pharmacological In Vitro Investigations of Novel Shikonin Derivatives with a Special Focus on Cyclopropane Bearing Derivatives.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 5, p. 2774, doi. 10.3390/ijms22052774
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The Isolation and Characterization of a Rhodacycle Intermediate Implicated in Metal-Catalyzed Reactions of Alkylidenecyclopropanes.
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- Angewandte Chemie, 2014, v. 126, n. 15, p. 4033, doi. 10.1002/ange.201310232
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[2+1] Cycloaddition Affording Methylene- and Vinylidenecyclopropane Derivatives: A Journey around the Reactivity of Metal-Phosphinito-Phosphinous Acid Complexes.
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- Chemical Record, 2017, v. 17, n. 4, p. 399, doi. 10.1002/tcr.201600081
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Synthesis of Phosphoryl-Substituted Cyclopropanes by Reaction of (1-Bromoethenyl)(diphenyl)phosphine Oxide with CH Acids.
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- Russian Journal of Organic Chemistry, 2022, v. 58, n. 12, p. 1989, doi. 10.1134/S1070428022120314
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Reactions of Activated Enynes with Diazomethane.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 10, p. 1575, doi. 10.1134/S107042802110002X
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One-Pot Ozonolytic Synthesis of Isoniazid Derivatives from (-)-α-Pinene and Δ³-Carene.
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- Russian Journal of Organic Chemistry, 2018, v. 54, n. 1, p. 146, doi. 10.1134/S1070428018010165
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Cyclopropane intermediates in the synthesis of chiral alcohols with methyl-branched carbon skeleton. Application in the synthesis of insect pheromones.
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- Russian Journal of Organic Chemistry, 2014, v. 50, n. 7, p. 934, doi. 10.1134/S1070428014070033
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Crystal structure of 2-benzoyl-3-(4-methoxyphenyl) cyclopropane-1,1-dicarbonitrile, C<sub>19</sub>H<sub>14</sub>N<sub>2</sub>O<sub>2</sub>.
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- Zeitschrift für Kristallographie / New Crystal Structures, 2017, v. 232, n. 6, p. 897, doi. 10.1515/ncrs-2017-0052
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Novel synthesis of highly functionalized cyclopentane derivatives via [3 + 2] cycloaddition reactions of donor–acceptor cyclopropanes and (E)-3-aryl-2-cyanoacrylates.
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- Journal of Chemical Research, 2019, v. 43, n. 1/2, p. 43, doi. 10.1177/1747519819831883
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Synthesis of novel spiro[cyclopropane-indolizine] derivatives via magnesium-mediated conjugate addition of bromoform.
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- Journal of Chemical Research, 2013, v. 37, n. 11, p. 681, doi. 10.3184/174751913X13814138618396
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In vitro human T cell responses to diphencyprone.
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- Contact Dermatitis (01051873), 2017, v. 76, n. 4, p. 251, doi. 10.1111/cod.12697
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New spirocyclopropane derivatives: synthesis and evaluation of their performances toward corrosion inhibition of mild steel in acidic media.
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- Research on Chemical Intermediates, 2020, v. 46, n. 6, p. 2881, doi. 10.1007/s11164-020-04108-9
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Synthesis of novel spiro[cyclopropane-pyrrolizin] derivatives via Mg-mediated conjugate addition of bromoform.
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- Research on Chemical Intermediates, 2015, v. 41, n. 4, p. 2345, doi. 10.1007/s11164-013-1350-6
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A New Strategy for the Synthesis of Organosilicon Compounds of Cyclopropane Derivatives.
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- Australian Journal of Chemistry, 2021, v. 74, n. 4, p. 245, doi. 10.1071/CH20203
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Zinc-Catalyzed Multicomponent Reactions: Easy Access to Furyl- Substituted Cyclopropane and 1,2-Dioxolane Derivatives.
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- European Journal of Organic Chemistry, 2016, p. 2681, doi. 10.1002/ejoc.201600393
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Zinc-Catalyzed Multicomponent Reactions: Easy Access to Furyl-Substituted Cyclopropane and 1,2-Dioxolane Derivatives.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 15, p. 2681, doi. 10.1002/ejoc.201600393
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Lewis-Acid-Catalysed Friedel-Crafts Alkylation of Donor-Acceptor Cyclopropanes with Electron-Rich Benzenes to Generate 1,1-Diarylalkanes.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 29, p. 6419, doi. 10.1002/ejoc.201500856
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Antiviral Cyclopropane Acids from Deep-Sea-Derived Fungus Aspergillus sydowii.
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- Marine Drugs, 2022, v. 20, n. 7, p. 410, doi. 10.3390/md20070410
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Synthesis, biological evaluation and molecular docking studies of some novel cyclopropane carbohydrazide derivatives as potential anticancer agents.
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- Journal of Chemical Sciences, 2016, v. 128, n. 6, p. 929, doi. 10.1007/s12039-016-1081-5
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Synthesis of Functionalized α‐Vinyl Aldehydes from Enaminones.
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- Angewandte Chemie, 2019, v. 131, n. 36, p. 12804, doi. 10.1002/ange.201906213
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Lewis Acid Catalyzed Enantioselective Desymmetrization of Donor–Acceptor <italic>meso</italic>‐Diaminocyclopropanes.
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- Angewandte Chemie, 2018, v. 130, n. 18, p. 5214, doi. 10.1002/ange.201800494
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SYNTHESIS BASED ON ETHYL CYANOACETATE.
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- Chemical Problems / Kimya Problemləri, 2023, v. 21, n. 4, p. 323, doi. 10.32737/2221-8688-2023-4-323-330
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Methanesulfonic Acid‐Catalyzed Friedel‐Crafts Alkylation: Towards Sustainable Synthesis of Arylalkanes from Donor–Acceptor Cyclopropane Ketones.
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- Asian Journal of Organic Chemistry, 2024, v. 13, n. 7, p. 1, doi. 10.1002/ajoc.202400116
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Regioselective Carbozincation and Further Functionalization of Allenamides Catalyzed by an N‐Heterocyclic Carbene (NHC)‐Copper Complex.
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- Asian Journal of Organic Chemistry, 2023, v. 12, n. 10, p. 1, doi. 10.1002/ajoc.202300372
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Additive‐Free Synthesis of Trifluoromethylated Spiro Cyclopropanes and Their Transformation into Trifluoromethylated Building Blocks.
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- Asian Journal of Organic Chemistry, 2021, v. 10, n. 6, p. 1536, doi. 10.1002/ajoc.202100207
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Piperidine‐Mediated [3+2] Cyclization of Donor‐Acceptor Cyclopropanes and β‐Nitrostyrenes: Access to Polysubsituted Cyclopentenes with High Diastereoselectivity.
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- Asian Journal of Organic Chemistry, 2021, v. 10, n. 6, p. 1395, doi. 10.1002/ajoc.202100149
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Recent Advances in the Synthesis of CF<sub>3</sub>‐ or HCF<sub>2</sub>‐Substituted Cyclopropanes.
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- Asian Journal of Organic Chemistry, 2021, v. 10, n. 3, p. 485, doi. 10.1002/ajoc.202000723
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Recent Developments on the Synthesis of Various Sulfur‐Containing Heterocycles via [3+2]‐ and [4+2]‐Cycloaddition Reactions with Thiocarbonyls.
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- Asian Journal of Organic Chemistry, 2020, v. 9, n. 10, p. 1466, doi. 10.1002/ajoc.202000238
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Synthesis of Trifluoromethyl‐Substituted Cyclopropanes via Inorganic Base‐Mediated Cycloaddition Reactions.
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- Asian Journal of Organic Chemistry, 2019, v. 8, n. 11, p. 2054, doi. 10.1002/ajoc.201900550
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Transition-Metal-Free Synthesis of Polysubstituted Cyclopropane Derivatives from N-Tosylhydrazones and their Cytotoxic Activities.
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- Asian Journal of Organic Chemistry, 2015, v. 4, n. 10, p. 1144, doi. 10.1002/ajoc.201500289
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CYCLOPROPANE DERIVATIVES OF SYNDIOTACTIC 1,2-POLYBUTADIENE.
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- Journal of Nature Science & Sustainable Technology, 2015, v. 9, n. 2, p. 331
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An Efficient Solvent-free Synthesis of Spiro-substituted Cyclopropanes by Grinding.
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- Organic Preparations & Procedures International, 2023, v. 55, n. 3, p. 288, doi. 10.1080/00304948.2022.2141042
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Cover Picture.
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- Chinese Journal of Chemistry, 2025, v. 43, n. 4, p. 361, doi. 10.1002/cjoc.202590041
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Copper‐Catalyzed Ring‐Opening Hydrosilylation and Hydroboration of Arylidenecyclopropanes.
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- Chinese Journal of Chemistry, 2025, v. 43, n. 4, p. 385, doi. 10.1002/cjoc.202400811
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Divergent Synthesis of N‐Heterocycles by Merging Borane‐Mediated Cyclopropane Ring‐Opening and Hydride Abstraction.
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- Chinese Journal of Chemistry, 2021, v. 39, n. 6, p. 1641, doi. 10.1002/cjoc.202100056
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Asymmetric Catalytic [3+2] Annulation of Donor‐Acceptor Cyclopropane with Cyclic Ketones: Facile Access to Enantioenriched 1‐Oxaspiro[4.5]decanes<sup>†</sup>.
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- Chinese Journal of Chemistry, 2020, v. 38, n. 12, p. 1629, doi. 10.1002/cjoc.202000277
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Catalyst-Controlled Switch in Chemo- and Diastereoselectivities: Annulations of Morita-Baylis-Hillman Carbonates from Isatins.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 6, p. 2147, doi. 10.1002/anie.201510825
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Thrilling Strain! Donor-Acceptor-Substituted Cyclobutanes for the Synthesis of (Hetero)Cyclic Compounds.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 17, p. 5009, doi. 10.1002/anie.201501135
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Protonated heterocyclic derivatives of cyclopropane and cyclopropanone: classical species, alternate sites, and ring fragmentation.
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- Canadian Journal of Chemistry, 2015, v. 93, n. 7, p. 708, doi. 10.1139/cjc-2015-0029
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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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A DFT study on the oxidation of cyclotrisilene by nitrous oxide: the σ- and π-bonds reactivity.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2020, v. 139, n. 1, p. 1, doi. 10.1007/s00214-019-2540-0
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