Works matching DE "CHIRAL centers"
Results: 343
General Anesthetics: Aspects of Chirality, Pharmacodynamics, and Pharmacokinetics.
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- Pharmaceuticals (14248247), 2025, v. 18, n. 2, p. 250, doi. 10.3390/ph18020250
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Rh(I)/Sulfoxide‐Imine‐Olefin Complex Catalyzed Enantioselective Allylic Alkylation of 2‐Fluoromalonate: Synthesis of Chiral α‐Fluorolactone Bearing Vicinal Stereogenic Centers.
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- Chemistry - A European Journal, 2024, v. 30, n. 68, p. 1, doi. 10.1002/chem.202402875
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Chirality at Metal in a Linear [Ag(NHC)<sub>2</sub>]<sup>+</sup> Complex: Stereogenic C−Ag−C Axis, Atropisomerism and Role of π‐π Interactions.
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- Chemistry - A European Journal, 2024, v. 30, n. 64, p. 1, doi. 10.1002/chem.202403239
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Unrevealing the Nitrogen Elusive Chirality of 3‐Sulfanyl and 3‐Sulfinyl N‐Tosyl Isoindolinones by ECD Spectra: An Experimental and Theoretical Investigation.
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- Chemistry - A European Journal, 2024, v. 30, n. 29, p. 1, doi. 10.1002/chem.202400232
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Stereoselective Synthesis of β, γ‐Fused Bicyclic γ‐Ureasultams via an Intramolecular Mannich and aza‐Michael Addition Cascade.
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- Chemistry - A European Journal, 2024, v. 30, n. 28, p. 1, doi. 10.1002/chem.202400438
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Silver‐Catalyzed Asymmetric Double Desymmetrization via Vinylogous Michael Addition of Prochiral α,α‐Dicyanoalkenes to Cyclopentendiones.
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- Chemistry - A European Journal, 2024, v. 30, n. 20, p. 1, doi. 10.1002/chem.202304078
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Chemistry and Biology of Podophyllotoxins: An Update.
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- Chemistry - A European Journal, 2024, v. 30, n. 4, p. 1, doi. 10.1002/chem.202302595
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A Bifunctional Coordination‐Chain‐Based Hydrogen‐Bonded Framework for Quantitative Enantioselective Sensing.
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- Chemistry - A European Journal, 2023, v. 29, n. 57, p. 1, doi. 10.1002/chem.202301892
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Combining Enantioselective Rh‐Catalyzed Conjugate Addition and Ir‐Catalyzed Allylic Alkylation in Stereodivergent, Multicomponent Coupling Reactions to Form Three Stereocenters.
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- Chemistry - A European Journal, 2023, v. 29, n. 36, p. 1, doi. 10.1002/chem.202300727
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Enantioselective Transformations from Nitriles to NH<sub>2</sub>‐α‐Tertiary Amines.
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- Chemistry - A European Journal, 2023, v. 29, n. 27, p. 1, doi. 10.1002/chem.202300451
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A Photochemical Macrocyclization Route to Asymmetric Strained [3.2] Paracyclophanes.
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- Chemistry - A European Journal, 2022, v. 28, n. 69, p. 1, doi. 10.1002/chem.202202577
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- Article
Titelbild: Enantiopure [6]‐Azairidahelicene by Dynamic Kinetic Resolution of a Configurationally Labile [4]‐Helicene (Angew. Chem. 26/2024).
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- Angewandte Chemie, 2024, v. 136, n. 26, p. 1, doi. 10.1002/ange.202408865
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Enantiopure [6]‐Azairidahelicene by Dynamic Kinetic Resolution of a Configurationally Labile [4]‐Helicene.
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- Angewandte Chemie, 2024, v. 136, n. 26, p. 1, doi. 10.1002/ange.202406663
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Supertwisted Chiral Gyroid Mesophase in Chiral Rod‐Like Compounds.
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- Angewandte Chemie, 2024, v. 136, n. 23, p. 1, doi. 10.1002/ange.202403156
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Asymmetric Carbene‐Alkyne Metathesis‐Mediated Cascade: Synthesis of Benzoxazine Polychiral Polyheterocycles and Discovery of a Novel Pain Blocker.
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- Angewandte Chemie, 2024, v. 136, n. 21, p. 1, doi. 10.1002/ange.202401189
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Diastereo‐ and Enantioselective Synthesis of Tetracyclic Cycloheptanols through (4+3) Annulation via C−C/C−H Activation Cascade.
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- Angewandte Chemie, 2024, v. 136, n. 13, p. 1, doi. 10.1002/ange.202317433
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Catalytic Asymmetric Synthesis of Atropisomers Bearing Multiple Chiral Elements: An Emerging Field.
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- Angewandte Chemie, 2024, v. 136, n. 3, p. 1, doi. 10.1002/ange.202311053
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Combinatorial Ligand Assisted Simultaneous Control of Axial and Central Chirality in Highly Stereoselective C−H Allylation.
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- Angewandte Chemie, 2024, v. 136, n. 2, p. 1, doi. 10.1002/ange.202310112
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Polymeric Carbon Nitride with Chirality Inherited from Supramolecular Assemblies.
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- Angewandte Chemie, 2023, v. 135, n. 40, p. 1, doi. 10.1002/ange.202311389
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Enantioselective Synthesis of 1,2‐Benzothiazine 1‐Imines via Ru<sup>II</sup>/Chiral Carboxylic Acid‐Catalyzed C−H Alkylation/Cyclization.
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- Angewandte Chemie, 2023, v. 135, n. 29, p. 1, doi. 10.1002/ange.202305480
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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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Iridium‐Catalyzed Chemo‐, Diastereo‐, and Enantioselective Allyl‐Allyl Coupling: Accessing All Four Stereoisomers of (E)‐1‐Boryl‐Substituted 1,5‐Dienes by Chirality Pairing.
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- Angewandte Chemie, 2023, v. 135, n. 13, p. 1, doi. 10.1002/ange.202218794
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- Article
Haipeng Lu.
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- Angewandte Chemie, 2023, v. 135, n. 12, p. 1, doi. 10.1002/ange.202300660
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- Article
Enantioselective Synthesis of Spirosilabicyclohexenes by Asymmetric Dual Ring Expansion of Spirosilabicyclobutane with Alkynes.
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- Angewandte Chemie, 2022, v. 134, n. 48, p. 1, doi. 10.1002/ange.202212889
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Full Control of the Chiral Overpass Effect in Helical Polymers: P/M Screw Sense Induction by Remote Chiral Centers After Bypassing the First Chiral Residue.
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- Angewandte Chemie, 2022, v. 134, n. 46, p. 1, doi. 10.1002/ange.202209953
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Berichtigung: Iron‐Catalyzed Cross‐Coupling of Propargyl Ethers with Grignard Reagents for the Synthesis of Functionalized Allenes and Allenols.
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- Angewandte Chemie, 2022, v. 134, n. 43, p. 1, doi. 10.1002/ange.202212750
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Cobalt(III)/Chiral Carboxylic Acid‐Catalyzed Enantioselective Synthesis of Benzothiadiazine‐1‐oxides via C−H Activation.
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- Angewandte Chemie, 2022, v. 134, n. 28, p. 1, doi. 10.1002/ange.202205341
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Highly Regio‐, Stereo‐, and Enantioselective Copper‐Catalyzed B−H Bond Insertion of α‐Silylcarbenes: Efficient Access to Chiral Allylic gem‐Silylboranes.
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- Angewandte Chemie, 2022, v. 134, n. 26, p. 1, doi. 10.1002/ange.202203343
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Asymmetric Defluoroallylation of 4‐Trifluoromethylpyridines Enabled by Umpolung C−F Bond Activation**.
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- Angewandte Chemie, 2022, v. 134, n. 21, p. 1, doi. 10.1002/ange.202201102
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Catalytic Asymmetric Homologation of 4‐Substituted Cyclohexanones with CF<sub>3</sub>CHN<sub>2</sub>: Enantioselective Synthesis of α‐Trifluoromethyl Cycloheptanones.
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- Angewandte Chemie, 2022, v. 134, n. 6, p. 1, doi. 10.1002/ange.202115098
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Dynamic Kinetic Asymmetric Transformation of Racemic Diastereomers: Diastereo‐ and Enantioconvergent Michael–Henry Reactions to Afford Spirooxindoles Bearing Furan‐Fused Rings.
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- Angewandte Chemie, 2021, v. 133, n. 39, p. 21426, doi. 10.1002/ange.202108734
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Asymmetric Alkylation of Ketones Catalyzed by Engineered TrpB.
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- Angewandte Chemie, 2021, v. 133, n. 39, p. 21582, doi. 10.1002/ange.202106938
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Copper‐Catalyzed Highly Selective Protoboration of CF<sub>3</sub>‐Containing 1,3‐Dienes.
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- Angewandte Chemie, 2021, v. 133, n. 37, p. 20539, doi. 10.1002/ange.202105896
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Chirality‐Dependent Second‐Order Nonlinear Optical Effect in 1D Organic–Inorganic Hybrid Perovskite Bulk Single Crystal.
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- Angewandte Chemie, 2021, v. 133, n. 36, p. 20174, doi. 10.1002/ange.202108171
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Rhodium‐Catalyzed C−H Activation‐Based Construction of Axially and Centrally Chiral Indenes through Two Discrete Insertions.
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- Angewandte Chemie, 2021, v. 133, n. 30, p. 16764, doi. 10.1002/ange.202105093
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Total Synthesis of (−)‐Arborisidine.
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- Angewandte Chemie, 2021, v. 133, n. 23, p. 12842, doi. 10.1002/ange.202101161
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A Concise Total Synthesis of (−)‐Berkelic Acid.
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- Angewandte Chemie, 2021, v. 133, n. 10, p. 5201, doi. 10.1002/ange.202014660
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A Green and Wide‐Scope Approach for Chiroptical Sensing of Organic Molecules through Biomimetic Recognition in Water.
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- Angewandte Chemie, 2020, v. 132, n. 52, p. 24025, doi. 10.1002/ange.202011566
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Enantioselective Intramolecular [2,3]‐Sigmatropic Rearrangement of Aldehydes via a Sulfonium Enamine Intermediate.
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- Angewandte Chemie, 2020, v. 132, n. 47, p. 21090, doi. 10.1002/ange.202010234
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Distinguishing Enantiomers by Tip‐Enhanced Raman Scattering: Chemically Modified Silver Tip with an Asymmetric Atomic Arrangement.
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- Angewandte Chemie, 2020, v. 132, n. 34, p. 14672, doi. 10.1002/ange.202005446
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Silver‐Triggered Activity of a Heterogeneous Palladium Catalyst in Oxidative Carbonylation Reactions.
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- Angewandte Chemie, 2020, v. 132, n. 26, p. 10477, doi. 10.1002/ange.202001809
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A Transient‐Directing‐Group Strategy Enables Enantioselective Reductive Heck Hydroarylation of Alkenes.
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- Angewandte Chemie, 2020, v. 132, n. 23, p. 8970, doi. 10.1002/ange.202001069
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Rhodium(III)‐Catalyzed Asymmetric Access to Spirocycles through C−H Activation and Axial‐to‐Central Chirality Transfer.
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- Angewandte Chemie, 2020, v. 132, n. 18, p. 7255, doi. 10.1002/ange.202000174
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Stimuli‐Responsive Circularly Polarized Organic Ultralong Room Temperature Phosphorescence.
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- Angewandte Chemie, 2020, v. 132, n. 12, p. 4786, doi. 10.1002/ange.201915164
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Chiral Overpass Induction in Dynamic Helical Polymers Bearing Pendant Groups with Two Chiral Centers.
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- Angewandte Chemie, 2020, v. 132, n. 11, p. 4567, doi. 10.1002/ange.201915213
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Chirality‐Embedded Nanographenes.
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- Angewandte Chemie, 2020, v. 132, n. 2, p. 679, doi. 10.1002/ange.201910040
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Asymmetric Synthesis of Oxa‐Bridged Oxazocines through a Catalytic Rh<sup>II</sup>/Zn<sup>II</sup> Relay [4+3] Cycloaddition Reaction.
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- Angewandte Chemie, 2019, v. 131, n. 51, p. 18609, doi. 10.1002/ange.201910898
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Detection and Chiral Recognition of α‐Hydroxyl Acid through <sup>1</sup>H and CEST NMR Spectroscopy Using a Ytterbium Macrocyclic Complex.
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- Angewandte Chemie, 2019, v. 131, n. 50, p. 18454, doi. 10.1002/ange.201912072
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Synthesis of Chiral Tetrasubstituted Azetidines from Donor–Acceptor Azetines via Asymmetric Copper(I)‐Catalyzed Imido‐Ylide [3+1]‐Cycloaddition with Metallo‐Enolcarbenes.
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- Angewandte Chemie, 2019, v. 131, n. 45, p. 16334, doi. 10.1002/ange.201909929
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Carbene‐Catalyzed Desymmetrization and Direct Construction of Arenes with All‐Carbon Quaternary Chiral Center.
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- Angewandte Chemie, 2019, v. 131, n. 44, p. 15925, doi. 10.1002/ange.201910183
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