Works matching DE "CHIRALITY element"
Results: 232
New dibenzocyclooctadiene lignan from Schisandra chinensis (Turcz.) Baill. fruits.
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- Applied Biological Chemistry, 2021, v. 64, n. 1, p. 1, doi. 10.1186/s13765-021-00618-1
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Low-frequency resonances of a chiral sphere filled with a metamaterial.
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- Journal of Communications Technology & Electronics, 2015, v. 60, n. 1, p. 12, doi. 10.1134/S1064226915010015
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All-round catalytic and atroposelective strategy via dynamic kinetic resolution for N-/2-/3-arylindoles.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-41299-2
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Diastereo- and atroposelective synthesis of N-arylpyrroles enabled by light-induced phosphoric acid catalysis.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-40491-8
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Diversity-oriented synthesis of P-stereogenic and axially chiral monodentate biaryl phosphines enabled by C-P bond cleavage.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-40138-8
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Data-driven design of new chiral carboxylic acid for construction of indoles with C-central and C–N axial chirality via cobalt catalysis.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-38872-0
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Copper-catalyzed asymmetric C(sp<sup>2</sup>)–H arylation for the synthesis of P- and axially chiral phosphorus compounds.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-37987-8
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Front Cover: Fluorine‐Labelled Spiro[3.3]heptane‐Derived Building Blocks: Is Single Fluorine the Best? (Eur. J. Org. Chem. 35/2021).
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 35, p. 4895, doi. 10.1002/ejoc.202101076
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Analysis of Interconversion between Atropisomers of Chiral Substituted 9,9'‐Bicarbazole.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 3, p. 449, doi. 10.1002/ejoc.202001385
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Blue Chemistry. Marine Polysaccharide Biopolymers in Asymmetric Catalysis: Challenges and Opportunities.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 25, p. 3779, doi. 10.1002/ejoc.201901924
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A-Ring-Modified 2-Hydroxyethylidene Previtamin D<sub>3</sub> Analogues: Synthesis and Biological Evaluation.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 3, p. 504, doi. 10.1002/ejoc.201601263
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Ancistrobrevinium A, the first N-methylated, cationic naphthylisoquinoline alkaloid, from the tropical liana Ancistrocladus abbreviatus (Ancistrocladaceae).
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- Natural Product Research, 2024, v. 38, n. 15, p. 2614, doi. 10.1080/14786419.2023.2194648
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Review: Separation and Pharmacology of Chiral Compounds in Traditional Chinese Medicine.
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- Analytical Letters, 2017, v. 50, n. 1, p. 33, doi. 10.1080/00032719.2016.1169540
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Ellagic Acid and Schisandrins: Natural Biaryl Polyphenols with Therapeutic Potential to Overcome Multidrug Resistance in Cancer.
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- Cells (2073-4409), 2021, v. 10, n. 2, p. 458, doi. 10.3390/cells10020458
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Chiral Dirhodium(II) Carboxylates: New Insights into the Effect of Ligand Stereo-Purity on Catalyst Structure and Enantioselectivity.
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- Catalysts (2073-4344), 2018, v. 8, n. 7, p. 268, doi. 10.3390/catal8070268
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Enzymes useful for chiral compound synthesis: structural biology, directed evolution, and protein engineering for industrial use.
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- Applied Microbiology & Biotechnology, 2016, v. 100, n. 13, p. 5747, doi. 10.1007/s00253-016-7603-8
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Current Distribution in a Gyrotropic Microstrip Structure when Excited by a Plane Electromagnetic Wave.
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- Doklady Physics, 2018, v. 63, n. 6, p. 231, doi. 10.1134/S1028335818060058
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(aS)-Glucosciadopitysin, a New Biflavonoid Glycoside from the Leaves of Ginkgo biloba and Osteogenic Activity of Bioflavonoids.
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- Plants (2223-7747), 2025, v. 14, n. 2, p. 261, doi. 10.3390/plants14020261
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Static and Dynamic Magnetization Investigation in Permalloy Electrodeposited onto High Resistive N-Type Silicon Substrates.
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- Coatings (2079-6412), 2017, v. 7, n. 2, p. 33, doi. 10.3390/coatings7020033
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Complexation-induced N‒P axial chirality in Sm(II) N-phosphine oxide-substituted imidazolylidene and imidazolinylidene complexes.
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- Canadian Journal of Chemistry, 2023, v. 101, n. 7, p. 429, doi. 10.1139/cjc-2022-0249
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Catalytic Kinetic Resolution of Biaryl Compounds.
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- Chemistry - A European Journal, 2015, v. 21, n. 33, p. 11644, doi. 10.1002/chem.201500869
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Simultaneous Induction of Axial and Planar Chirality in Arene-Chromium Complexes by Molybdenum-Catalyzed Enantioselective Ring-Closing Metathesis.
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- Chemistry - A European Journal, 2015, v. 21, n. 13, p. 4954, doi. 10.1002/chem.201500226
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Imidazole-Peptide Foldamers: Parabolic Dependence of the Folding Process on the Water Content of the Solvent.
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- Chemistry - A European Journal, 2015, v. 21, n. 11, p. 4333, doi. 10.1002/chem.201406277
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Breaking the Odd-Even Effect in the Self-Assembly of Linear Bis(benzamides).
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- Chemistry - A European Journal, 2014, v. 20, n. 45, p. 14599, doi. 10.1002/chem.201404040
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Bioactive atropisomers: Unraveling design strategies and synthetic routes for drug discovery.
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- Medicinal Research Reviews, 2024, v. 44, n. 5, p. 1971, doi. 10.1002/med.22037
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Trityl-Containing Alcohols—An Efficient Chirality Transmission Process from Inductor to the Stereodynamic Propeller and their Solid-State Structural Diversity.
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- Molecules, 2020, v. 25, n. 3, p. 707, doi. 10.3390/molecules25030707
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Heteroaromatic N-Oxides in Asymmetric Catalysis: A Review.
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- Molecules, 2020, v. 25, n. 2, p. 330, doi. 10.3390/molecules25020330
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Single-component color-tunable circularly polarized organic afterglow through chiral clusterization.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-28070-9
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Catalytic atroposelective synthesis of axially chiral benzonitriles via chirality control during bond dissociation and CN group formation.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-021-27813-4
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Single-component color-tunable circularly polarized organic afterglow through chiral clusterization.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-28070-9
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Catalytic atroposelective synthesis of axially chiral benzonitriles via chirality control during bond dissociation and CN group formation.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-021-27813-4
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Lineage-Specific Chiral Biases of Human Embryonic Stem Cells during Differentiation.
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- Stem Cells International, 2018, p. 1, doi. 10.1155/2018/1848605
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THE HOMFLY POLYNOMIAL OF CLASSICAL PRETZEL LINKS AND ITS APPLICATION TO CHIRALITY.
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- Journal of Knot Theory & Its Ramifications, 2013, v. 22, n. 13, p. 1, doi. 10.1142/S0218216513500764
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Chiral PSiSi‐Ligand Enabled Iridium‐Catalyzed Atroposelective Intermolecular C−H Silylation.
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- Angewandte Chemie, 2023, v. 135, n. 36, p. 1, doi. 10.1002/ange.202307812
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Dynamic Kinetic Resolution of 2‐(Quinolin‐8‐yl)Benzaldehydes: Atroposelective Iridium‐Catalyzed Transfer Hydrogenative Allylation.
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- Angewandte Chemie, 2023, v. 135, n. 35, p. 1, doi. 10.1002/ange.202306981
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The First Enantiomeric Stereogenic Sulfur‐Chiral Organic Ferroelectric Crystals.
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- Angewandte Chemie, 2023, v. 135, n. 31, p. 1, doi. 10.1002/ange.202306732
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Dynamic Axial‐to‐Helical Communication Mechanism in Poly[(allenylethynylenephenylene)acetylene]s under External Stimuli.
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- Angewandte Chemie, 2023, v. 135, n. 29, p. 1, doi. 10.1002/ange.202303329
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Copper‐Catalyzed Radical Enantioselective Synthesis of γ‐Butyrolactones with Two Non‐vicinal Carbon Stereocenters.
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- Angewandte Chemie, 2023, v. 135, n. 28, p. 1, doi. 10.1002/ange.202304275
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Organocatalytic Atroposelective Cross‐Coupling of 1‐Azonaphthalenes and 2‐Naphthols.
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- Angewandte Chemie, 2023, v. 135, n. 25, p. 1, doi. 10.1002/ange.202303128
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Construction of Axially Chiral Arylpyrroles via Atroposelective Diyne Cyclization.
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- Angewandte Chemie, 2023, v. 135, n. 23, p. 1, doi. 10.1002/ange.202303670
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Direct Catalytic Asymmetric and Regiodivergent N1‐ and C3‐Allenylic Alkylation of Indoles.
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- Angewandte Chemie, 2023, v. 135, n. 21, p. 1, doi. 10.1002/ange.202300844
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Construction of Acyclic All‐Carbon Quaternary Stereocenters and 1,3‐Nonadjacent Stereoelements via Organo/Metal Dual Catalyzed Asymmetric Allenylic Substitution of Aldehydes.
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- Angewandte Chemie, 2023, v. 135, n. 20, p. 1, doi. 10.1002/ange.202300756
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Stereospecific Synthesis of Enantiopure [6]Helicene Containing a Seven‐Membered Ring and [7]Helicene by Acid‐Promoted Stepwise Alkyne Annulations of Doubly Axial‐Chiral Precursors**.
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- Angewandte Chemie, 2023, v. 135, n. 18, p. 1, doi. 10.1002/ange.202301836
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Catalytic Asymmetric Synthesis of Axially Chiral Diaryl Ethers through Enantioselective Desymmetrization.
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- Angewandte Chemie, 2023, v. 135, n. 14, p. 1, doi. 10.1002/ange.202300481
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Towards Axially Chiral Pyrazole‐Based Phosphorus Scaffolds by Dipeptide‐Phosphonium Salt Catalysis.
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- Angewandte Chemie, 2023, v. 135, n. 13, p. 1, doi. 10.1002/ange.202215720
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The Asymmetric Buchwald–Hartwig Amination Reaction.
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- Angewandte Chemie, 2023, v. 135, n. 9, p. 1, doi. 10.1002/ange.202216863
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Asymmetric Hydrophosphinylation of Alkynes: Facile Access to Axially Chiral Styrene‐Phosphines.
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- Angewandte Chemie, 2023, v. 135, n. 3, p. 1, doi. 10.1002/ange.202215820
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(SCp)Rhodium‐Catalyzed Asymmetric Satoh–Miura Reaction for Building‐up Axial Chirality: Counteranion‐Directed Switching of Reaction Pathways.
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- Angewandte Chemie, 2023, v. 135, n. 3, p. 1, doi. 10.1002/ange.202214460
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Phosphoric Acid‐Catalyzed Enantioselective Synthesis of Axially Chiral Anthrone‐based Compounds.
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- Angewandte Chemie, 2023, v. 135, n. 1, p. 1, doi. 10.1002/ange.202213914
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Rhodium‐Catalyzed Dynamic Kinetic Asymmetric Hydrosilylation to Access Silicon‐Stereogenic Center.
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- Angewandte Chemie, 2022, v. 134, n. 51, p. 1, doi. 10.1002/ange.202214147
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