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Frontispiz: Long‐Lived Circularly Polarized Phosphorescence in Helicene‐NHC Rhenium(I) Complexes: The Influence of Helicene, Halogen, and Stereochemistry on Emission Properties.
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- Angewandte Chemie, 2020, v. 132, n. 22, p. 1, doi. 10.1002/ange.202082261
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Innentitelbild: Long‐Lived Circularly Polarized Phosphorescence in Helicene‐NHC Rhenium(I) Complexes: The Influence of Helicene, Halogen, and Stereochemistry on Emission Properties (Angew. Chem. 22/2020).
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- Angewandte Chemie, 2020, v. 132, n. 22, p. 8382, doi. 10.1002/ange.202002387
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Long‐Lived Circularly Polarized Phosphorescence in Helicene‐NHC Rhenium(I) Complexes: The Influence of Helicene, Halogen, and Stereochemistry on Emission Properties.
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- Angewandte Chemie, 2020, v. 132, n. 22, p. 8472, doi. 10.1002/ange.202002387
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Stereoselective Syntheses, Structures, and Properties of Extremely Distorted Chiral Nanographenes Embedding Hextuple Helicenes.
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- Angewandte Chemie, 2020, v. 132, n. 8, p. 3290, doi. 10.1002/ange.201913200
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Chiral Atropisomeric Indenocorannulene Bowls: Critique of the Cahn–Ingold–Prelog Conception of Molecular Chirality.
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- Angewandte Chemie, 2018, v. 130, n. 22, p. 6580, doi. 10.1002/ange.201801325
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Enantiopure Cycloiridiated Complexes Bearing a Pentahelicenic N-Heterocyclic Carbene and Displaying Long-Lived Circularly Polarized Phosphorescence.
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- Angewandte Chemie, 2017, v. 129, n. 28, p. 8348, doi. 10.1002/ange.201704263
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Iron Alkynyl Helicenes: Redox-Triggered Chiroptical Tuning in the IR and Near-IR Spectral Regions and Suitable for Telecommunications Applications.
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- Angewandte Chemie, 2016, v. 128, n. 28, p. 8194, doi. 10.1002/ange.201601633
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Combining Organocatalysis with Central-to-Axial Chirality Conversion: Atroposelective Hantzsch-Type Synthesis of 4-Arylpyridines.
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- Angewandte Chemie, 2016, v. 128, n. 4, p. 1423, doi. 10.1002/ange.201509967
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Atropisomeric Chiral Probes to Study the Supramolecular Organization in Porphyrin Self-Assemblies.
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- European Journal of Organic Chemistry, 2012, v. 2012, n. 33, p. 6526, doi. 10.1002/ejoc.201200985
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Thiyl Radical Mediated Racemization of Benzylic Amines.
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- European Journal of Organic Chemistry, 2006, v. 2006, n. 14, p. 3242, doi. 10.1002/ejoc.200600120
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Green Self-Assembling Porphyrins and Chlorins as Mimics of the Natural Bacteriochlorophylls c, d, and e.
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- European Journal of Organic Chemistry, 2004, v. 2004, n. 18, p. 3919
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Atropisomeric N‐Heterocyclic Carbene‐Palladium(II) Complexes: Influence of the Backbone Substitution.
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- European Journal of Inorganic Chemistry, 2024, v. 27, n. 12, p. 1, doi. 10.1002/ejic.202300780
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Metallahelicenes: Easily Accessible Helicene Derivatives with Large and Tunable Chiroptical Properties.
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- Angewandte Chemie International Edition, 2010, v. 49, n. 1, p. 99, doi. 10.1002/anie.200905099
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Acid/Base-Triggered Switching of Circularly Polarized Luminescence and Electronic Circular Dichroism in Organic and Organometallic Helicenes.
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- Chemistry - A European Journal, 2015, v. 21, n. 4, p. 1673, doi. 10.1002/chem.201405176
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Static and Dynamic Properties of 1,1′-Bi-2-naphthol and Its Conjugated Acids and Bases.
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- Chemistry - A European Journal, 2014, v. 20, n. 45, p. 14816, doi. 10.1002/chem.201402686
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A Racemic and Enantiopure Unsymmetric Diiron(III) Complex with a Chiral o-Carborane-Based Pyridylalcohol Ligand: Combined Chiroptical, Magnetic, and Nonlinear Optical Properties.
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- Chemistry - A European Journal, 2014, v. 20, n. 4, p. 1081, doi. 10.1002/chem.201303037
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Diastereo- and Enantioselective Synthesis of Organometallic Bis(helicene)s by a Combination of CH Activation and Dynamic Isomerization.
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- Chemistry - A European Journal, 2013, v. 19, n. 49, p. 16722, doi. 10.1002/chem.201302479
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EthylenedithioTetrathiafulvaleneHelicenes: Electroactive Helical Precursors with Switchable Chiroptical Properties.
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- Chemistry - A European Journal, 2013, v. 19, n. 39, p. 13160, doi. 10.1002/chem.201301095
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Enantioselective Syntheses of the Proposed Structures of Kopeolin and Kopeolone.
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- Chemistry - A European Journal, 2013, v. 19, n. 32, p. 10632, doi. 10.1002/chem.201300711
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Multifunctional and Reactive Enantiopure Organometallic Helicenes: Tuning Chiroptical Properties by Structural Variations of Mono- and Bis(platinahelicene)s.
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- Chemistry - A European Journal, 2011, v. 17, n. 50, p. 14178, doi. 10.1002/chem.201101866
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Persistent Mixed-Valence [(TTF)<sub>2</sub>]<sup>+.</sup> Dyad of a Chiral Bis(binaphthol)-tetrathiafulvalene (TTF) Derivative.
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- Chemistry - A European Journal, 2010, v. 16, n. 27, p. 8020, doi. 10.1002/chem.200902050
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Chirality in Dynamic Supramolecular Nanotubes Induced by a Chiral Solvent.
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- Chemistry - A European Journal, 2010, v. 16, n. 1, p. 173, doi. 10.1002/chem.200902399
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Cellulose chiral induction during the synthesis of cellulose N-phthaloyl-amino acid esters.
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- Cellulose, 2013, v. 20, n. 4, p. 2057, doi. 10.1007/s10570-013-9946-y
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Synthesis, structural characterization, and chiroptical properties of planarly and axially chiral boranils.
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- Chirality, 2023, v. 35, n. 4, p. 227, doi. 10.1002/chir.23537
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Transition metal complexes bearing atropisomeric saturated NHC ligands.
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- Chirality, 2022, v. 34, n. 1, p. 13, doi. 10.1002/chir.23378
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Chiroptical properties of anionic and neutral nickel(II) bis(dithiolene) complexes based on methyl and dimethyl‐dddt ligands.
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- Chirality, 2022, v. 34, n. 1, p. 4, doi. 10.1002/chir.23375
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Multigram‐scale HPLC enantioseparation as a rescue pathway for circumventing racemization problem during enantioselective synthesis of ethyl 3,4‐dihydro‐2H‐1,4‐benzoxazine‐2‐carboxylate.
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- Chirality, 2021, v. 33, n. 7, p. 324, doi. 10.1002/chir.23313
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Enantiopure ethyl 2,3‐dibromopropionate: Enantioselective synthesis vs preparative HPLC enantioseparation of racemate on multigram scale.
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- Chirality, 2020, v. 32, n. 8, p. 1045, doi. 10.1002/chir.23260
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Enantiorecognition on solid chiral selectors using microbatch technology: an example of limitation in case of strong association in the racemate.
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- Biomedical Chromatography, 2005, v. 19, n. 6, p. 434, doi. 10.1002/bmc.502
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Dinuclear Rhenium Complexes with a Bridging Helicene‐bis‐bipyridine Ligand: Synthesis, Structure, and Photophysical and Chiroptical Properties.
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- ChemPlusChem, 2020, v. 85, n. 11, p. 2446, doi. 10.1002/cplu.202000559
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Cover Feature: Helical Bisphosphinites in Asymmetric Tsuji‐Trost Allylation: a Remarkable P:Pd Ratio Effect (ChemCatChem 21/2021).
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- ChemCatChem, 2021, v. 13, n. 21, p. 4457, doi. 10.1002/cctc.202101516
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Helical Bisphosphinites in Asymmetric Tsuji‐Trost Allylation: a Remarkable P:Pd Ratio Effect.
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- ChemCatChem, 2021, v. 13, n. 21, p. 4543, doi. 10.1002/cctc.202101072
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Front Cover: Aryl Fluoroalkyl Sulfoxides: Optical Stability and pK<sub>a</sub> Measurement (Eur. J. Org. Chem. 36/2021).
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 36, p. 5017, doi. 10.1002/ejoc.202100935
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Aryl Fluoroalkyl Sulfoxides: Optical Stability and pK<sub>a</sub> Measurement.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 36, p. 5019, doi. 10.1002/ejoc.202100816
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Front Cover: Helically Chiral NHC‐Gold(I) Complexes: Synthesis, Chiroptical Properties and Electronic Features of the [5]Helicene‐Imidazolylidene Ligand (Eur. J. Org. Chem. 34/2021).
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 34, p. 4767, doi. 10.1002/ejoc.202100934
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Helically Chiral NHC‐Gold(I) Complexes: Synthesis, Chiroptical Properties and Electronic Features of the [5]Helicene‐Imidazolylidene Ligand.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 34, p. 4769, doi. 10.1002/ejoc.202100722
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Allosteric Guest Binding in Chiral Zirconium(IV) Double Decker Porphyrin Cages.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 4, p. 607, doi. 10.1002/ejoc.202001392
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A HELIXOL‐Derived Bisphosphinite Ligand: Synthesis and Application in Gold‐Catalyzed Enynes Cycloisomerization.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 11, p. 2129, doi. 10.1002/ejoc.201801722
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Enantioselective Complexation of Chiral Oxirane Derivatives by an Enantiopure Cryptophane in Water.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 13, p. 1601, doi. 10.1002/ejoc.201800142
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Organocopper-Triggered Cyclisation of Conjugated Diene-ynes: Diastereo- and Enantioselective Synthesis of Indenes.
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- Advanced Synthesis & Catalysis, 2015, v. 357, n. 16/17, p. 3611, doi. 10.1002/adsc.201500556
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Synthesis of Allenes Bearing Phosphine Oxide Groups and Investigation of Their Reactivity toward Gold Complexes.
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- Advanced Synthesis & Catalysis, 2015, v. 357, n. 10, p. 2213, doi. 10.1002/adsc.201500345
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Copper Carbenoid, Reactant and Catalyst for One-Pot Diazo Ester Coupling Cascade Rearrangement of Enediynes: Formation of Two Contiguous Tetrasubstituted Stereocenters.
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- Advanced Synthesis & Catalysis, 2012, v. 354, n. 10, p. 1987, doi. 10.1002/adsc.201200045
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N-Octanoyldimethylglycine Trifluoroethyl Ester, an Acyl Donor Leading to Highly Enantioselective Protease-Catalysed Kinetic Resolution of Amines.
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- Advanced Synthesis & Catalysis, 2012, v. 354, n. 9, p. 1759, doi. 10.1002/adsc.201100993
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Rational Design of New Conjugated Polymers with Main Chain Chirality for Efficient Optoelectronic Devices: Carbo[6]Helicene and Indacenodithiophene Copolymers as Model Compounds.
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- Advanced Materials, 2024, v. 36, n. 25, p. 1, doi. 10.1002/adma.202314337
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Enantiopure encaged Verkade's superbases: Synthesis, chiroptical properties, and use as chiral derivatizing agent.
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- Chirality, 2020, v. 32, n. 2, p. 139, doi. 10.1002/chir.23156
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Synthesis and chiroptical properties of organometallic complexes of helicenic N‐heterocyclic carbenes.
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- Chirality, 2019, v. 31, n. 12, p. 1005, doi. 10.1002/chir.23143
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Synthesis, resolution, and chiroptical properties of hemicryptophane cage controlling the chirality of propeller arrangement of a C<sub>3</sub> triamide unit.
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- Chirality, 2019, v. 31, n. 11, p. 910, doi. 10.1002/chir.23131
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Chiroptical study of cryptophanes subjected to self‐encapsulation.
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- Chirality, 2019, v. 31, n. 7, p. 481, doi. 10.1002/chir.23079
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Effect of substituents on the configurational stability of the stereogenic nitrogen in metal(II) complexes of α‐amino acid Schiff bases.
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- Chirality, 2019, v. 31, n. 5, p. 401, doi. 10.1002/chir.23066
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Redox‐triggered chiroptical switching activity of ruthenium(III)‐bis‐(β‐diketonato) complexes bearing a bipyridine‐helicene ligand.
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- Chirality, 2018, v. 30, n. 5, p. 592, doi. 10.1002/chir.22835
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