Works matching DE "DIASTEREOISOMERS"
Results: 848
Preparation of Optically Active Allothreonine by Separating from a Diastereoisomeric Mixture with Threonine.
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- Bioscience, Biotechnology & Biochemistry, 2010, v. 74, n. 10, p. 2106, doi. 10.1271/bbb.100295
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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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New Polar Constituents of the Pupae of the Silkworm Bombyx mon L. I. Isolation and Identification of Methionine Sulfoxide, Methionine Sulfone, and γ-Cyclic di-L-Glutamate.
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- Bioscience, Biotechnology & Biochemistry, 2007, v. 71, n. 12, p. 3055, doi. 10.1271/bbb.70457
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Synthesis of the Four Stereoisomers of 2,6-Dimethyloctane-1,8-dioic Acid, a Component of the Copulation Release Pheromone of the Cowpea Weevil, Callosobruchus maculatus.
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- Bioscience, Biotechnology & Biochemistry, 2005, v. 69, n. 12, p. 2401, doi. 10.1271/bbb.69.2401
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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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Chiral Sulfoximine Mediated Cobalt‐Catalyzed Atropselective C−H Annulation of Ynamides.
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- Chemistry - A European Journal, 2024, v. 30, n. 55, p. 1, doi. 10.1002/chem.202401639
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Exploring a De Novo Route to Bradyrhizose: Synthesis and Isomeric Equilibrium of Bradyrhizose Diastereomers<sup>≠</sup>.
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- Chemistry - A European Journal, 2024, v. 30, n. 33, p. 1, doi. 10.1002/chem.202400886
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Diastereoselective Synthesis of α‐Aryl‐Substituted LnDOTA Chelates from Achiral Starting Materials by Deracemization Under Mild Conditions.
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- Chemistry - A European Journal, 2023, v. 29, n. 60, p. 1, doi. 10.1002/chem.202301887
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Enantio‐ and Diastereomerically Pure Titanocenes by Dynamic Conformational Locking.
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- Chemistry - A European Journal, 2023, v. 29, n. 48, p. 1, doi. 10.1002/chem.202301645
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Front Cover: Facile Synthesis of Enantiomerically Pure P‐Chiral 1‐Alkoxy‐2,3‐dihydrophospholes via Nucleophilic P‐N Bond Cleavage of a 1‐Phospha‐2‐azanorbornene (Chem. Eur. J. 45/2023).
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- Chemistry - A European Journal, 2023, v. 29, n. 45, p. 1, doi. 10.1002/chem.202301936
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Facile Synthesis of Enantiomerically Pure P‐Chiral 1‐Alkoxy‐2,3‐dihydrophospholes via Nucleophilic P‐N Bond Cleavage of a 1‐Phospha‐2‐azanorbornene.
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- Chemistry - A European Journal, 2023, v. 29, n. 45, p. 1, doi. 10.1002/chem.202300790
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The Aldol‐Tishchenko Reaction of Butanone, Cyclobutanone and a 3‐Pentanone Derived Sulfinylimine and DFT Calculations of the Stereo‐determining Step.
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- Chemistry - A European Journal, 2023, v. 29, n. 22, p. 1, doi. 10.1002/chem.202203029
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Asymmetric Ruthenium Catalysis Enables Fluorophores with Point Chirality Displaying CPL Properties**.
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- Chemistry - A European Journal, 2023, v. 29, n. 10, p. 1, doi. 10.1002/chem.202203243
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Preparation of N‐2‐Nitrophenylsulfenyl Imino Peptides and Their Catalyst‐Controlled Diastereoselective Indolylation.
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- Chemistry - A European Journal, 2023, v. 29, n. 8, p. 1, doi. 10.1002/chem.202203120
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Anion‐Driven Programmable Chiral Self‐Sorting in Metal‐Organic Cages and Structural Transformations between Heterochiral and Homochiral Cages.
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- Chemistry - A European Journal, 2023, v. 29, n. 6, p. 1, doi. 10.1002/chem.202203085
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Stereodivergent Total Syntheses of (+)‐Mycaperoxides C, D, G Methyl Ester and (−)‐Mycaperoxide B.
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- Chemistry - A European Journal, 2023, v. 29, n. 6, p. 1, doi. 10.1002/chem.202203004
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Chelating Phosphorus–An O, C, O‐Coordinating Pincer‐Type Ligand Coordinating P<sup>III</sup> and P<sup>V</sup> Centres.
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- Chemistry - A European Journal, 2022, v. 28, n. 58, p. 1, doi. 10.1002/chem.202201447
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Synergistic Palladium/Copper‐Catalyzed 1,4‐Difunctionalization of 1,3‐Dienes for Stereodivergent Construction of 1,5‐Nonadjacent Stereocenters.
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- Angewandte Chemie, 2024, v. 136, n. 21, p. 1, doi. 10.1002/ange.202402843
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Diastereoselective Self‐Assembly of Low‐Symmetry Pd<sub>n</sub>L<sub>2n</sub> Nanocages through Coordination‐Sphere Engineering.
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- Angewandte Chemie, 2023, v. 135, n. 51, p. 1, doi. 10.1002/ange.202315451
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Asymmetric Radical Oxyboration of β‐Substituted Styrenes via Late‐Stage Stereomutation.
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- Angewandte Chemie, 2023, v. 135, n. 48, p. 1, doi. 10.1002/ange.202313770
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Synthesis of a Blue‐Emissive Azaborathia[9]helicene by Silicon‐Boron Exchange from Unusual Atropisomeric Teraryls.
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- Angewandte Chemie, 2023, v. 135, n. 30, p. 1, doi. 10.1002/ange.202304291
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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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Dynamic‐to‐Static Planar Chirality Conversion in Pillar[5]arenes Regulated by Guest Solvents or Amplified by Crystallization.
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- Angewandte Chemie, 2023, v. 135, n. 19, p. 1, doi. 10.1002/ange.202217971
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Protoglobin‐Catalyzed Formation of cis‐Trifluoromethyl‐Substituted Cyclopropanes by Carbene Transfer.
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- Angewandte Chemie, 2023, v. 135, n. 4, p. 1, doi. 10.1002/ange.202208936
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Picolinamides and Iodoalkynes Enable Palladium‐Catalyzed syn‐Aminoalkynylation of Di‐ and Trisubstituted Alkenes to Give Pyrrolidines.
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- Angewandte Chemie, 2022, v. 134, n. 38, p. 1, doi. 10.1002/ange.202204535
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Bioinspired Asymmetric Total Synthesis of Emeriones A–C**.
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- Angewandte Chemie, 2022, v. 134, n. 32, p. 1, doi. 10.1002/ange.202205878
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Divergent Asymmetric Synthesis of Panowamycins, TM‐135, and Veramycin F Using C−H Insertion with Donor/Donor Carbenes.
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- Angewandte Chemie, 2022, v. 134, n. 25, p. 1, doi. 10.1002/ange.202203072
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Total Synthesis and Stereochemistry Assignment of Nucleoside Antibiotic A‐94964.
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- Angewandte Chemie, 2022, v. 134, n. 14, p. 1, doi. 10.1002/ange.202200818
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Stereodivergent Attached‐Ring Synthesis via Non‐Covalent Interactions: A Short Formal Synthesis of Merrilactone A.
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- Angewandte Chemie, 2022, v. 134, n. 3, p. 1, doi. 10.1002/ange.202114514
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Asymmetric Synthesis of 2,2‐Difluorotetrahydrofurans through Palladium‐Catalyzed Formal [3+2] Cycloaddition.
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- Angewandte Chemie, 2021, v. 133, n. 44, p. 23833, doi. 10.1002/ange.202111376
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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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Enantioselective Synthesis of Pyroglutamic Acid Esters from Glycinate via Carbonyl Catalysis.
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- Angewandte Chemie, 2021, v. 133, n. 19, p. 10682, doi. 10.1002/ange.202017306
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Configurational Analysis by Residual Dipolar Couplings: Critical Assessment of "Structural Noise" from Thermal Vibrations.
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- Angewandte Chemie, 2021, v. 133, n. 7, p. 3454, doi. 10.1002/ange.202011081
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Synthesis of Pyrrolidines by a Csp<sup>3</sup>‐Csp<sup>3</sup>/Csp<sup>3</sup>‐N Transition‐Metal‐Free Domino Reaction of Boronic Acids with γ‐Azido‐N‐Tosylhydrazones.
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- Angewandte Chemie, 2021, v. 133, n. 3, p. 1293, doi. 10.1002/ange.202010528
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The Formosalides: Structure Determination by Total Synthesis.
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- Angewandte Chemie, 2021, v. 133, n. 1, p. 450, doi. 10.1002/ange.202011472
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Probing Long‐Range Anisotropic Interactions: a General and Sign‐Sensitive Strategy to Measure <sup>1</sup>H–<sup>1</sup>H Residual Dipolar Couplings as a Key Advance for Organic Structure Determination.
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- Angewandte Chemie, 2020, v. 132, n. 13, p. 5354, doi. 10.1002/ange.201915278
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Rhodium‐Catalyzed Enantioselective [4+2] Cycloadditions of Vinylcarbenes with Dienes.
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- Angewandte Chemie, 2020, v. 132, n. 12, p. 4967, doi. 10.1002/ange.201914354
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An Enamide‐Based Domino Reaction for a Highly Stereoselective Synthesis of Tetrahydropyrans.
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- Angewandte Chemie, 2019, v. 131, n. 37, p. 13190, doi. 10.1002/ange.201907565
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Enantioselective Total Synthesis of Pseudopteroxazole and Ileabethoxazole.
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- Angewandte Chemie, 2019, v. 131, n. 23, p. 7927, doi. 10.1002/ange.201901651
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Synthesis of Selenium‐Triphosphates (dNTPαSe) for More Specific DNA Polymerization.
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- Angewandte Chemie, 2019, v. 131, n. 23, p. 7917, doi. 10.1002/ange.201901113
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Prediction of Major Regio‐, Site‐, and Diastereoisomers in Diels–Alder Reactions by Using Machine‐Learning: The Importance of Physically Meaningful Descriptors.
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- Angewandte Chemie, 2019, v. 131, n. 14, p. 4563, doi. 10.1002/ange.201806920
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Synthesis and In Vitro Neuroprotector Activity of Diastereoisomers of a Dimeric Dipeptide Mimetic of Nerve Growth Factor GK-2.
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- Pharmaceutical Chemistry Journal, 2018, v. 52, n. 8, p. 704, doi. 10.1007/s11094-018-1885-3
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Synthesis and Antileukemic Activity of N-Phthaloyl-2-Aminoalcohols.
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- Pharmaceutical Chemistry Journal, 2004, v. 38, n. 3, p. 120, doi. 10.1023/B:PHAC.0000034298.06587.30
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STEREOCHEMICAL FEATURES OF REPRODUCING A STABLE DIMERIC MOTIF IN THE CRYSTALS OF BODIPY DERIVATIVES IN TRANSITIONING FROM AN ACHIRAL TO A CHIRAL SUBSTITUTE IN MESO-POSITION.
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- Journal of Structural Chemistry, 2022, v. 63, n. 12, p. 1913, doi. 10.1134/S0022476622120010
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Structure of new derivatives of perhydropyrimidine-2-ones and intermolecular interactions in their crystals.
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- Journal of Structural Chemistry, 2017, v. 58, n. 2, p. 283, doi. 10.1134/S0022476617020093
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Structure of methyl-7-methoxy-7-phenyl-6- endo-halobicyclo[3.1.1]heptane-6- exo-carboxylate diastereomers in single crystals.
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- Journal of Structural Chemistry, 2007, v. 48, n. 6, p. 1124, doi. 10.1007/s10947-007-0180-z
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NHC-Ni catalyzed 1,3- and 1,4-diastereodivergent heterocycle synthesis from hetero-substituted enyne.
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- Communications Chemistry, 2020, v. 3, n. 1, p. 1, doi. 10.1038/s42004-020-0299-9
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The Intermolecular Pauson‐Khand Reaction of Sugar‐Derived Azaenynes: A Case of Total Diastereoselectivity.
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- Journal of Carbohydrate Chemistry, 2006, v. 25, n. 2/3, p. 197, doi. 10.1080/07328300600732733
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Oligodeoxynucleotides Containing Diastereomeric O2′,C3′‐linked Bicyclic Nucleotide Units for Functionalization of the Major Groove of Nucleic Acid Duplexes: A Summary and Novel Derivatives*.
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- Journal of Carbohydrate Chemistry, 2005, v. 24, n. 4-6, p. 475, doi. 10.1081/CAR-200067044
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Synthesis of 3-O-β-D- Glucopyranosyl-(3R)- hydroxybutanolide (Kinsenoside) and 3-O-β- D-Glucopyranosyl-(3S)- hydroxybutanolide (Goodyeroside A).
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- Journal of Carbohydrate Chemistry, 2005, v. 24, n. 1, p. 73, doi. 10.1081/CAR-200050541
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