Works about ENANTIOMERS
Results: 3218
Mechanistic Insights into Sugar Racemization and Oxidative Degradation via Fenton and Alkaline Peroxide Systems.
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- Chemistry (2624-8549), 2025, v. 7, n. 1, p. 2, doi. 10.3390/chemistry7010002
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Synthesis and Bioassay of the Eight Analogues of the CH503 Male Pheromone (3-Acetoxy-ll,19-octacosadien-l-ol) of the Drosophila melanogaster Fruit Fly.
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- Bioscience, Biotechnology & Biochemistry, 2013, v. 77, n. 9, p. 1931, doi. 10.1271/bbb.130383
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Efficient Preparation of (/?)-3-Hydroxypentanenitrile with High Enantiomeric Excess by Enzymatic Reduction with Subsequent Enhancement of the Optical Purity by Lipase-Catalyzed Ester Hydrolysis.
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- Bioscience, Biotechnology & Biochemistry, 2012, v. 76, n. 9, p. 1796, doi. 10.1271/bbb.120331
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Comparative Activities of the 5-Enantiomer and Racemic Forms of Equol on Bone Fragility in Ovariectomized Mice.
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- Bioscience, Biotechnology & Biochemistry, 2012, v. 76, n. 5, p. 1018, doi. 10.1271/bbb.110973
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Asymmetric Synthesis and Sensory Evaluation of Sedanenolide.
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- Bioscience, Biotechnology & Biochemistry, 2011, v. 75, n. 8, p. 1502, doi. 10.1271/bbb.110206
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Structures and Properties of a Diastereoisomeric Molecular Compound of (2S,3S)- and (2R,3S)-N-Acetyl-2-amino-3-methylpentanoic Acids.
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- Bioscience, Biotechnology & Biochemistry, 2009, v. 73, n. 10, p. 2293, doi. 10.1271/bbb.90389
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Isolation and Structural Elucidation of a New Cyclohexenone Compound from Lasiodiplodia theobromae.
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- Bioscience, Biotechnology & Biochemistry, 2009, v. 73, n. 8, p. 1890, doi. 10.1271/bbb.90218
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Syntheses of Bioactive Bisabolane-Type Cryptomeria japonica Sesquiterpenes.
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- Bioscience, Biotechnology & Biochemistry, 2009, v. 73, n. 3, p. 588, doi. 10.1271/bbb.80671
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Synthesis and Bioactivity of Potassium β-D-Glucopyranosyl 12-Hydroxy Jasmonate and Related Compounds.
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- Bioscience, Biotechnology & Biochemistry, 2008, v. 72, n. 11, p. 2867, doi. 10.1271/bbb.80338
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Synthesis of FF8181-A.
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- Bioscience, Biotechnology & Biochemistry, 2008, v. 72, n. 10, p. 2708, doi. 10.1271/bbb.80351
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First Stereoselective Synthesis of meso-Secoisolariciresinol and Comparison of Its Biological Activity with (+) and (-)-Secoisolariciresinol.
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- Bioscience, Biotechnology & Biochemistry, 2007, v. 71, n. 12, p. 2962, doi. 10.1271/bbb.70358
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Effect of Benzylic Oxygen on the Cytotoxic Activity for Colon 26 Cell Line of Phenolic Lignans.
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- Bioscience, Biotechnology & Biochemistry, 2006, v. 70, n. 12, p. 2942, doi. 10.1271/bbb.60353
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Enantioselective Synthesis of the (1S,5R)-Enantiomer of Litseaverticillols A and B.
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- Bioscience, Biotechnology & Biochemistry, 2006, v. 70, n. 10, p. 2564, doi. 10.1271/bbb.60253
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Enzymatic Synthesis of L-Pipecolic Acid by Δ¹-Piperideine-2-carboxylate Reductase from Pseudomonas putida.
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- Bioscience, Biotechnology & Biochemistry, 2006, v. 70, n. 9, p. 2296, doi. 10.1271/bbb.60125
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Absolute Configuration of Hydroxycitric Acid Produced by Microorganisms.
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- Bioscience, Biotechnology & Biochemistry, 2006, v. 70, n. 8, p. 1972, doi. 10.1271/bbb.50701
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Synthesis of a Glandular Secretion of the Civet Cat, (2S,6S)-(6-Methyltetrahydropyran-2-yl)acetic Acid and Its Enantiomer, by Using the Yeast-Reduction Product and Recovered Substrate from Yeast Reduction.
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- Bioscience, Biotechnology & Biochemistry, 2006, v. 70, n. 3, p. 712, doi. 10.1271/bbb.70.712
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Production of (R)-3-Amino-3-phenylpropionic Acid and (S)-3-Amino-3-phenyl-propionic Acid from (R,S)-N-Acetyl-3-amino-3-phenylpropionic Acid Using Microorganisms Having Enantiomer-Specific Amidohydrolyzing Activity.
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- Bioscience, Biotechnology & Biochemistry, 2006, v. 70, n. 1, p. 99, doi. 10.1271/bbb.70.99
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Inhibitory Effect of Mispyric Acid on Mammalian DNA Polymerases.
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- Bioscience, Biotechnology & Biochemistry, 2005, v. 69, n. 8, p. 1534, doi. 10.1271/bbb.69.1534
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Formation of trans-Verbenol and Verbenone from α-Pinene Catalysed by Immobilised Picea abies Cells.
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- Bioscience, Biotechnology & Biochemistry, 2005, v. 69, n. 2, p. 321, doi. 10.1271/bbb.69.321
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Synthesis, Absolute Configuration and Biological Activities of Both Enantiomers of 2-(5,7-Dichloro-3-indolyl)propionic Acid: a Novel Dichloroindole Auxin and Antiauxin.
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- Bioscience, Biotechnology & Biochemistry, 2004, v. 68, n. 6, p. 1287, doi. 10.1271/bbb.68.1287
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Niotransformation of &alpha-Isomethylionone to 1-(2,6,6-Trimethyl-2-cyclohexen-1-yl)propan-2-one.
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- Bioscience, Biotechnology & Biochemistry, 2004, v. 68, n. 5, p. 1164, doi. 10.1271/bbb.68.1164
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Synthesis of All Four Stereoisomers of 3-Amino-2-hydroxybutanoic Acids.
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- Bioscience, Biotechnology & Biochemistry, 2004, v. 68, n. 3, p. 714, doi. 10.1271/bbb.68.714
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Chiral Discrimination of Branched-chain Fatty Acids by Reversed-phase HPLC after Labeling with a Chiral Fluorescent Conversation Reagent.
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- Bioscience, Biotechnology & Biochemistry, 2004, v. 68, n. 1, p. 153, doi. 10.1271/bbb.68.153
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Synthetic Racemate and Enantiomers of Cytosporone E, a Metabolite of an Endophytic Fungus, Show Indistinguishably Weak Antimicrobial Activity.
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- Bioscience, Biotechnology & Biochemistry, 2003, v. 67, n. 12, p. 2584, doi. 10.1271/bbb.67.2584
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Synthesis and Absolute Configuration of (-)-3-Butyl-7-hydroxyphthalide, a Cytotoxic Metabolite of Penicillium vulpinum.
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- Bioscience, Biotechnology & Biochemistry, 2003, v. 67, n. 10, p. 2240, doi. 10.1271/bbb.67.2240
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Synthesis of the Enantiomers of 21-Methyl-7-hentriacontanone and a Stereoisomeric Mixture of 5-Acetoxy-19-methylnonacosane, Candidates for the Female Sex Pheromone of the Screwworm Fly, Cochliomyia hominivorax.
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- Bioscience, Biotechnology & Biochemistry, 2003, v. 67, n. 10, p. 2224, doi. 10.1271/bbb.67.2224
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Synthesis of the Racemate and Both Enantiomers of Massoilactone.
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- Bioscience, Biotechnology & Biochemistry, 2003, v. 67, n. 10, p. 2210, doi. 10.1271/bbb.67.2210
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Systematic Strategy for the Synthesis of Cyanobacterin and Its Stereoisomers. 1. Asymmetric Total Synthesis of Dechloro-cyanobacterin and Its Enantiomer.
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- Bioscience, Biotechnology & Biochemistry, 2003, v. 67, n. 10, p. 2183, doi. 10.1271/bbb.67.2183
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New Method for Synthesizing the Intermediates to 5-HETE from Yeast-mediated Reduction Products by Employing Baeyer-Villiger Oxidation with Complete Retention of Enantiomeric Excess.
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- Bioscience, Biotechnology & Biochemistry, 2003, v. 67, n. 9, p. 1959, doi. 10.1271/bbb.67.1959
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Asymmetric Chloronicotinyl Insecticide, 1-[1-(6-Chloro-3-pyridyl)ethyl]-2-nitroiminoimidazolidine: Preparation, Resolution and Biological Activities toward Insects and Their Nerve Preparations.
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- Bioscience, Biotechnology & Biochemistry, 2003, v. 67, n. 5, p. 980, doi. 10.1271/bbb.67.980
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Unique Transitions in Morphology and Characteristics of Porous Poly(Lactic Acid) Enantiomers.
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- Macromolecular Chemistry & Physics, 2018, v. 219, n. 7, p. 1, doi. 10.1002/macp.201700547
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Central-to-Axial Chirality Transfer-Induced CD Sensor for Chiral Recognition and ee Value Detection of 1,2-DACH Enantiomers.
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- Macromolecular Chemistry & Physics, 2015, v. 216, n. 19, p. 1925, doi. 10.1002/macp.201500236
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D‐π‐A Type [7]Helicene‐like Imide Derivatives with Tunable Photophysical Properties and Circularly Polarized Luminescence.
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- Chemistry - A European Journal, 2024, v. 30, n. 71, p. 1, doi. 10.1002/chem.202403292
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Twist along Central C−C Bonds in a Series of Fully π‐Fused Propellanes.
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- Chemistry - A European Journal, 2024, v. 30, n. 68, p. 1, doi. 10.1002/chem.202402828
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Synthesis Strategies, Preparation Methods, and Applications of Chiral Metal‐Organic Frameworks.
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- Chemistry - A European Journal, 2024, v. 30, n. 34, p. 1, doi. 10.1002/chem.202401091
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Structure and Chiroptical Properties of Anthra[1,2‐a]anthracene‐1‐yl Dimers as New Biaryls.
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- Chemistry - A European Journal, 2024, v. 30, n. 31, p. 1, doi. 10.1002/chem.202400929
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Construction and Application of a Pepsin‐Functionalized Covalent Organic Framework with Prominent Chiral Recognition Ability.
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- Chemistry - A European Journal, 2024, v. 30, n. 15, p. 1, doi. 10.1002/chem.202303827
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Total Chemical Synthesis of the SARS‐CoV‐2 Spike Receptor‐Binding Domain.
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- Chemistry - A European Journal, 2024, v. 30, n. 3, p. 1, doi. 10.1002/chem.202302969
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Asymmetric Transfer Hydrogenation as a Key Step in the Synthesis of the Phosphonic Acid Analogs of Aminocarboxylic Acids.
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- Chemistry - A European Journal, 2023, v. 29, n. 72, p. 1, doi. 10.1002/chem.202302171
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Front Cover: Chiral‐at‐Metal Racemization Unraveled for MX<sub>2</sub>(a‐chel)<sub>2</sub> by means of a Computational Analysis of MoO<sub>2</sub>(acnac)<sub>2</sub> (Chem. Eur. J. 66/2023).
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- Chemistry - A European Journal, 2023, v. 29, n. 66, p. 1, doi. 10.1002/chem.202303604
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One‐Pot Synthesis of Helical Azaheptalene and Chiroptical Switching of an Isolable Radical Cation**.
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- Chemistry - A European Journal, 2023, v. 29, n. 48, p. 1, doi. 10.1002/chem.202301759
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Crystallographic Deciphering of Spontaneous Self‐Assembly of Achiral Calciphores to Chiral Complexes.
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- Chemistry - A European Journal, 2023, v. 29, n. 10, p. 1, doi. 10.1002/chem.202203127
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Enantiomeric Resolution and Enantiomer Isolation of H<sub>2</sub>TPPS4 J‐Aggregate from Aqueous Solution Is Enabled by Vortexes.
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- Chemistry - A European Journal, 2023, v. 29, n. 7, p. 1, doi. 10.1002/chem.202202337
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Design and Synthesis of a Ferrocene‐Based Diol Library and Application in the Hetero‐Diels‐Alder Reaction.
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- Chemistry - A European Journal, 2023, v. 29, n. 6, p. 1, doi. 10.1002/chem.202203006
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Bright Organic Mechanoluminescence and Remarkable Mechanofluorochromism from Circularly Polarized TADF Enantiomers with Aggregation‐Induced Emission Properties**.
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- Chemistry - A European Journal, 2023, v. 29, n. 5, p. 1, doi. 10.1002/chem.202202594
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Chiral‐at‐Metal Silver‐Mediated Base Pairs: Metal‐Centred Chirality versus DNA Helical Chirality.
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- Chemistry - A European Journal, 2023, v. 29, n. 3, p. 1, doi. 10.1002/chem.202202630
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Synthesis of Isomeric Tb<sup>3+</sup>‐Phthalocyanine Double‐Decker Complexes Depending on the Difference in the Direction of Coordination Plane and Their Magnetic Properties.
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- Chemistry - A European Journal, 2023, v. 29, n. 1, p. 1, doi. 10.1002/chem.202203272
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YfeX – A New Platform for Carbene Transferase Development with High Intrinsic Reactivity.
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- Chemistry - A European Journal, 2022, v. 28, n. 65, p. 1, doi. 10.1002/chem.202201474
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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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Cover Feature: Enantiodivergent Chemoenzymatic Dynamic Kinetic Resolution: Conversion of Racemic Propargyl Alcohols into Both Enantiomers (Chem. Eur. J. 60/2022).
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- Chemistry - A European Journal, 2022, v. 28, n. 60, p. 1, doi. 10.1002/chem.202203161
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