Works matching DE "CYCLOPROPANE derivatives"
Results: 113
"Boron Ylide" Enables Stereoselective Construction of gem‐Diborylcyclopropanes.
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- Angewandte Chemie, 2025, v. 137, n. 3, p. 1, doi. 10.1002/ange.202415301
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Stereoselective Synthesis of a Promising Flower-Inducing KODA Analog, (9R,12S,13R,15Z)-9-Hydroxy-12,13-methylene-10-oxooctadec-15-enoic Acid.
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- Bioscience, Biotechnology & Biochemistry, 2013, v. 77, n. 6, p. 1354, doi. 10.1271/bbb.130243
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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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Catalytic Enantioselective Synthesis of Functionalized Cyclopropanes from α‐Substituted Allyl Sulfones with Donor‐Acceptor or Diacceptor Diazo Reagents.
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- Chemistry - A European Journal, 2022, v. 28, n. 42, p. 1, doi. 10.1002/chem.202201254
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Enantioselective Tsuji‐Trost α‐Fluoroallylation of Amino Acid Esters with Gem‐Difluorinated Cyclopropanes.
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- Angewandte Chemie, 2024, v. 136, n. 23, p. 1, doi. 10.1002/ange.202402038
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Photocatalytic O‐ to S‐Rearrangement of Tertiary Cyclopropanols.
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- Angewandte Chemie, 2024, v. 136, n. 17, p. 1, doi. 10.1002/ange.202402912
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Taming of Furfurylidenes by Chiral Bismuth‐Rhodium Paddlewheel Catalysts. Preparation and Functionalization of Optically Active 1,1‐Disubstituted (Trifluoromethyl)cyclopropanes.
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- Angewandte Chemie, 2023, v. 135, n. 44, p. 1, doi. 10.1002/ange.202311598
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Rhodium‐Catalyzed Regio‐ and Diastereoselective [3+2] Cycloaddition of gem‐Difluorinated Cyclopropanes with Internal Olefins.
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- Angewandte Chemie, 2023, v. 135, n. 32, p. 1, doi. 10.1002/ange.202307129
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Cobalt‐Catalyzed Facial‐Selective Hydroalkylation of Cyclopropenes.
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- Angewandte Chemie, 2023, v. 135, n. 30, p. 1, doi. 10.1002/ange.202306381
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Catalytic Diastereo‐ and Enantioselective Cyclopropanation of gem‐Dihaloalkanes and Terminal Olefins.
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- Angewandte Chemie, 2023, v. 135, n. 28, p. 1, doi. 10.1002/ange.202305987
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Diastereoselective Synthesis of Cyclopropanes from Carbon Pronucleophiles and Alkenes.
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- Angewandte Chemie, 2023, v. 135, n. 21, p. 1, doi. 10.1002/ange.202303032
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Diboron(4)‐Catalyzed Remote [3+2] Cycloaddition of Cyclopropanes via Dearomative/Rearomative Radical Transmission through Pyridine.
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- Angewandte Chemie, 2022, v. 134, n. 52, p. 1, doi. 10.1002/ange.202214507
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Nickel‐Hydride‐Catalyzed Diastereo‐ and Enantioselective Hydroalkylation of Cyclopropenes.
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- Angewandte Chemie, 2022, v. 134, n. 46, p. 1, doi. 10.1002/ange.202210560
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(4+3) Annulation of Donor‐Acceptor Cyclopropanes and Azadienes: Highly Stereoselective Synthesis of Azepanones.
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- Angewandte Chemie, 2022, v. 134, n. 36, p. 1, doi. 10.1002/ange.202209006
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Catalysis with Supramolecular Carbon‐Bonding Interactions.
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- Angewandte Chemie, 2021, v. 133, n. 42, p. 22899, doi. 10.1002/ange.202108973
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Palladium‐Catalyzed Cascade to Benzoxepins by Using Vinyl‐Substituted Donor–Acceptor Cyclopropanes.
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- Angewandte Chemie, 2021, v. 133, n. 26, p. 14531, doi. 10.1002/ange.202102862
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Rhodium Catalyzed Regioselective C−H Allylation of Simple Arenes via C−C Bond Activation of Gem‐difluorinated Cyclopropanes.
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- Angewandte Chemie, 2021, v. 133, n. 19, p. 10720, doi. 10.1002/ange.202016258
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Biocatalytic Strategy for the Highly Stereoselective Synthesis of CHF<sub>2</sub>‐Containing Trisubstituted Cyclopropanes.
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- Angewandte Chemie, 2021, v. 133, n. 13, p. 7148, doi. 10.1002/ange.202015895
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An Enzymatic Platform for the Highly Enantioselective and Stereodivergent Construction of Cyclopropyl‐δ‐lactones.
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- Angewandte Chemie, 2020, v. 132, n. 48, p. 21818, doi. 10.1002/ange.202007953
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Divergent Total Synthesis of Euphoranginol C, Euphoranginone D, ent‐Trachyloban‐3β‐ol, ent‐Trachyloban‐3‐one, Excoecarin E, and ent‐16α‐Hydroxy‐atisane‐3‐one.
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- Angewandte Chemie, 2020, v. 132, n. 45, p. 20091, doi. 10.1002/ange.202009128
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A Vinyl Cyclopropane Ring Expansion and Iridium‐Catalyzed Hydrogen Borrowing Cascade.
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- Angewandte Chemie, 2020, v. 132, n. 28, p. 11435, doi. 10.1002/ange.202003614
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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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The use of durian seeds (Durio zibethinus Murr) as flour products from Tolitoli and Donggala Regencies.
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- Journal of Natural Resources & Environment Management / Jurnal Pengelolaan Sumberdaya Alam dan Lingkungan, 2022, v. 12, n. 3, p. 478, doi. 10.29244/jpsl.12.3.478-484
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Discovery of aminopyridine-containing spiro derivatives as EGFR mutations inhibitors.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2019, v. 34, n. 1, p. 1233, doi. 10.1080/14756366.2019.1634704
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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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Enhanced tolerance to inhibitors of Escherichia coli by heterologous expression of cyclopropane-fatty acid-acyl-phospholipid synthase (cfa) from Halomonas socia.
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- Bioprocess & Biosystems Engineering, 2020, v. 43, n. 5, p. 909, doi. 10.1007/s00449-020-02287-8
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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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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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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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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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Benzotriazolium Ylides‐Assisted Multicomponent Diastereoselective Synthesis of Activated Tetra‐ and Penta‐Substituted Cyclopropanes.
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- Asian Journal of Organic Chemistry, 2024, v. 13, n. 4, p. 1, doi. 10.1002/ajoc.202400012
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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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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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A Macrocyclic Peptide Library with a Structurally Constrained Cyclopropane‐containing Building Block Leads to Thiol‐independent Inhibitors of Phosphoglycerate Mutase.
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- Chemistry - An Asian Journal, 2020, v. 15, n. 17, p. 2631, doi. 10.1002/asia.202000700
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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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Front Cover: Photocatalyzed Energy Transfer for Atom Economical Synthesis of O‐Bridged Tricyclo‐Fused Cyclopropane Derivatives (Eur. J. Org. Chem. 45/2023).
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- European Journal of Organic Chemistry, 2023, v. 26, n. 45, p. 1, doi. 10.1002/ejoc.202301188
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Photocatalyzed Energy Transfer for Atom Economical Synthesis of O‐Bridged Tricyclo‐Fused Cyclopropane Derivatives.
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- European Journal of Organic Chemistry, 2023, v. 26, n. 45, p. 1, doi. 10.1002/ejoc.202300805
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Enantiospecific Total Synthesis of (−)‐Hyacinthacine A<sub>1</sub> and (+)‐Hyacinthacine A<sub>1</sub> and Their Homologues Using Nitrogen Substituted Donor–Acceptor Cyclopropane.
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- European Journal of Organic Chemistry, 2023, v. 26, n. 41, p. 1, doi. 10.1002/ejoc.202300818
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