Works matching DE "ENANTIOSELECTIVE catalysis"
Results: 3861
Synthesis and Applications of Functionalized Magnetic Nanomaterials in Enantioseparation.
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- Separation & Purification Reviews, 2019, v. 48, n. 1, p. 14, doi. 10.1080/15422119.2017.1419257
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Asymmetric Synthesis of Axially Chiral N, N‐1,2‐Pentatomic Heterobiaryl Diamines by an Organocatalytic Arylation Reaction.
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- Chemistry - A European Journal, 2024, v. 30, n. 70, p. 1, doi. 10.1002/chem.202402843
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Enantioselective Synthesis of Benzodihydrofurans Bearing Axial and Central Stereogenic Elements.
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- Chemistry - A European Journal, 2024, v. 30, n. 69, p. 1, doi. 10.1002/chem.202403374
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Steric Engineering of Rotaxane Catalysts: Benefits and Limits of Using the Mechanical Bond in Catalyst Design.
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- Chemistry - A European Journal, 2024, v. 30, n. 67, p. 1, doi. 10.1002/chem.202402717
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Efficient Synthesis of a C<sub>2</sub>‐Symmetric 2,2′‐Bipyridine‐α,α′‐1‐t–butyl‐diol Ligand by Stereoselective Double Hydrogen Transfer to a 2,2′‐Bipyridine‐diketone.
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- Chemistry - A European Journal, 2024, v. 30, n. 56, p. 1, doi. 10.1002/chem.202402449
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Endowing Metal‐Organic Coordination Materials with Chiroptical Activity by a Chiral Anion Strategy.
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- Chemistry - A European Journal, 2024, v. 30, n. 28, p. 1, doi. 10.1002/chem.202400685
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Cavity Catalysis of an Enantioselective Reaction under Vibrational Strong Coupling.
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- Chemistry - A European Journal, 2024, v. 30, n. 26, p. 1, doi. 10.1002/chem.202400607
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Atroposelective Chan–Evans–Lam Amination.
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- Chemistry - A European Journal, 2024, v. 30, n. 16, p. 1, doi. 10.1002/chem.202304378
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Highly Enantioselective Synthesis of Pharmaceuticals at Chiral‐Encoded Metal Surfaces.
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- Chemistry - A European Journal, 2023, v. 29, n. 61, p. 1, doi. 10.1002/chem.202302054
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Latent Pronucleophiles in Lewis Base Catalysis: Enantioselective Allylation of Silyl Enol Ethers with Allylic Fluorides.
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- Chemistry - A European Journal, 2023, v. 29, n. 37, p. 1, doi. 10.1002/chem.202300641
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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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Frontispiece: Catalytic Enantioselective [3+2] Cycloaddition of N‐Metalated Azomethine Ylides.
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- Chemistry - A European Journal, 2023, v. 29, n. 28, p. 1, doi. 10.1002/chem.202300296
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Light‐triggered Modulation of Supramolecular Chirality.
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- Chemistry - A European Journal, 2023, v. 29, n. 22, p. 1, doi. 10.1002/chem.202203794
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Cover Feature: Brønsted Acid versus Phase‐Transfer Catalysis in the Enantioselective Transannular Aminohalogenation of Enesultams (Chem. Eur. J. 62/2022).
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- Chemistry - A European Journal, 2022, v. 28, n. 62, p. 1, doi. 10.1002/chem.202203257
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Brønsted Acid versus Phase‐Transfer Catalysis in the Enantioselective Transannular Aminohalogenation of Enesultams.
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- Chemistry - A European Journal, 2022, v. 28, n. 62, p. 1, doi. 10.1002/chem.202202267
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Menthol.
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- Chemie in unserer Zeit, 2013, v. 47, n. 3, p. 174, doi. 10.1002/ciuz.201300599
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Heterogeneous Ag<sub>x</sub>Cd<sub>y</sub>S‐AgCd Nanoparticles with Chiral Bias for Enhanced Photocatalytic Efficiency.
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- Advanced Functional Materials, 2023, v. 33, n. 4, p. 1, doi. 10.1002/adfm.202210046
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Plasmonic Nanoparticles with Supramolecular Recognition.
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- Advanced Functional Materials, 2020, v. 30, n. 2, p. N.PAG, doi. 10.1002/adfm.201902082
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Learning epistatic interactions from sequence-activity data to predict enantioselectivity.
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- Journal of Computer-Aided Molecular Design, 2017, v. 31, n. 12, p. 1085, doi. 10.1007/s10822-017-0090-x
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A promising enantioselective Diels–Alder dienophile by computer-assisted rational design: 2,5-diphenyl-1-vinyl-borolane.
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- Journal of Computer-Aided Molecular Design, 2004, v. 18, n. 3, p. 209, doi. 10.1023/B:JCAM.0000035200.30340.41
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Spontaneous transfer of chirality in an atropisomerically enriched two-axis system.
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- Nature, 2014, v. 509, n. 7498, p. 71, doi. 10.1038/nature13189
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Organic chemistry: Catalysis marches on.
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- Nature, 2014, v. 508, n. 7496, p. 324, doi. 10.1038/nature13225
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Asymmetric synthesis from terminal alkenes by cascades of diboration and cross-coupling.
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- Nature, 2014, v. 505, n. 7483, p. 386, doi. 10.1038/nature12781
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Simple organic molecules as catalysts for enantioselective synthesis of amines and alcohols.
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- Nature, 2013, v. 494, n. 7436, p. 216, doi. 10.1038/nature11844
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Asymmetric spiroacetalization catalysed by confined Brønsted acids.
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- Nature, 2012, v. 483, n. 7389, p. 315, doi. 10.1038/nature10932
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Asymmetric additions to dienes catalysed by a dithiophosphoric acid.
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- Nature, 2011, v. 470, n. 7333, p. 245, doi. 10.1038/nature09723
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Biotransformation of Aromatic Ketones by Linum usitatissimum.
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- Chemistry of Natural Compounds, 2015, v. 51, n. 4, p. 752, doi. 10.1007/s10600-015-1400-y
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Enantioselective synthesis of 11-homodrim-7-en-9 α,12,13-triol.
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- Chemistry of Natural Compounds, 2011, v. 47, n. 4, p. 574, doi. 10.1007/s10600-011-9998-x
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Stereoselective synthesis of an alarm pheromone of Grematogaster ants using (4 S)-4-benzyloxazolidinone as chiral auxiliary.
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- Chemistry of Natural Compounds, 2010, v. 46, n. 1, p. 83, doi. 10.1007/s10600-010-9531-7
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Carbene-catalyzed asymmetric Friedel–Crafts alkylation-annulation sequence and rapid synthesis of indole-fused polycyclic alkaloids.
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- Communications Chemistry, 2019, v. 2, n. 1, p. N.PAG, doi. 10.1038/s42004-019-0188-2
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Pyrrolidines and piperidines bearing chiral tertiary alcohols by nickel-catalyzed enantioselective reductive cyclization of N-alkynones.
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- Communications Chemistry, 2018, v. 1, n. 1, p. N.PAG, doi. 10.1038/s42004-018-0092-1
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Enantioselective Photochromism under Circularly Polarized Light.
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- ChemPhotoChem, 2019, v. 3, n. 6, p. 347, doi. 10.1002/cptc.201900068
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Enantioselective disruption of the endocrine system by Cis-Bifenthrin in the male mice.
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- Environmental Toxicology, 2015, v. 30, n. 7, p. 746, doi. 10.1002/tox.21954
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Toxicity and enantiospecific differences of two β-blockers, propranolol and metoprolol, in the embryos and larvae of zebrafish ( Danio rerio).
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- Environmental Toxicology, 2014, v. 29, n. 12, p. 1367, doi. 10.1002/tox.21867
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The role of oxidative stress in enantiomer-specific, bifenthrin-induced cytotoxicity in PC12 cells.
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- Environmental Toxicology, 2011, v. 26, n. 3, p. 271, doi. 10.1002/tox.20553
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Factors affecting the phytoaccumulation of weathered, soil-borne organic contaminants: analyses at the ex Planta and in Planta sides of the plant root.
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- Plant & Soil, 2007, v. 291, n. 1/2, p. 143, doi. 10.1007/s11104-006-9182-4
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Phenanthroline-based fluorescence sensors for Eu<sup>3+</sup> ion and subsequent enantioselective discriminating of malate.
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- Supramolecular Chemistry, 2018, v. 30, n. 12, p. 994, doi. 10.1080/10610278.2018.1517877
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Inherently chiral phosphonate cavitands as enantioselective receptors for mono-methylated L-amino acids.
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- Supramolecular Chemistry, 2018, v. 30, n. 7, p. 600, doi. 10.1080/10610278.2017.1417991
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Crown-ether-modified cyclic dipeptides as supramolecular chiral catalysts.
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- Supramolecular Chemistry, 2018, v. 30, n. 3, p. 184, doi. 10.1080/10610278.2017.1392521
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Enantioselective recognition of electrochemically inactive phenylalanine by thiolated-cyclodextrin/ferrocene-coated gold nanoparticles.
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- Supramolecular Chemistry, 2011, v. 23, n. 6, p. 455, doi. 10.1080/10610278.2010.544738
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Remote chiral transfer into [2+2] and [2+4] cycloadditions within self-assembled molecular flasks.
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- Supramolecular Chemistry, 2011, v. 23, n. 3/4, p. 199, doi. 10.1080/10610278.2010.521833
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Self-sorting among the diastereoisomers of a M3L2 subphthalocyanine capsule.
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- Supramolecular Chemistry, 2009, v. 21, n. 1/2, p. 44, doi. 10.1080/10610270802478263
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Enantioselective Fluorescent Recognition of Amino Alcohol Based on Calix[4]arenes Bearing Diphenylethylenediamine Units.
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- Supramolecular Chemistry, 2008, v. 20, n. 3, p. 265, doi. 10.1080/10610270701200180
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Chiral memory and self-replication study of porphyrin and bilirubin aggregates formed on polypeptide matrices.
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- Supramolecular Chemistry, 2008, v. 20, n. 7, p. 643, doi. 10.1080/10610270701647919
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Synthesis and Enantioselective Recognition of a Calix[5]arene-based Chiral Receptor.
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- Supramolecular Chemistry, 2008, v. 20, n. 1/2, p. 51, doi. 10.1080/10610270701742553
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Nonsymmetrically Substituted Uranyl-Salophen Receptors: New Opportunities for Molecular Recognition and Catalysis.
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- Supramolecular Chemistry, 2007, v. 19, n. 1/2, p. 79, doi. 10.1080/10610270600977714
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Bio-inspired Calix[6]Arene-Zinc Funnel Complexes.
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- Supramolecular Chemistry, 2003, v. 15, n. 7/8, p. 573, doi. 10.1080/10610270310001605160
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Manufacture of zinc oxide/chiral poly(amide-imide)-functionalized amino acid and thiazole bionanocomposites: Using ionic liquid and ultrasonic irradiation.
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- Journal of Thermoplastic Composite Materials, 2015, v. 28, n. 5, p. 672, doi. 10.1177/0892705713487187
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New “camphor” Michael acceptor.
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- Russian Journal of Organic Chemistry, 2004, v. 40, n. 9, p. 1373, doi. 10.1007/s11178-005-0023-3
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Enantioselective Hydrogenation over Chiral Cobalt Complexes with (+)-(1S,2S,5R)-Neomenthyldiphenylphosphine and (–)-(R,R)-2,2-Dimethyl-4,5-bis(diphenylphosphinomethyl)-1,3-dioxolane.
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- Russian Journal of Organic Chemistry, 2004, v. 40, n. 7, p. 973, doi. 10.1023/B:RUJO.0000045187.83680.fe
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