Works matching DE "STEREOSPECIFICITY"
Results: 209
Synthesis of Syndiotactic Macrocyclic Poly(methyl methacrylate) via Transformation of the Growing Terminal in Stereospecific Anionic Polymerization.
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- Macromolecular Chemistry & Physics, 2017, v. 218, n. 12, p. n/a, doi. 10.1002/macp.201700041
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Stereospecific Styrene Polymerization by Methylalumoxane-Activated Ti (IV) N-Trimethylsilylamido Complexes Bearing the N-Biphenyl or N-(6-(2-(Diethylboryl)phenyl)-Pyrid-2-yl) Motif.
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- Macromolecular Chemistry & Physics, 2014, v. 215, n. 20, p. 2007, doi. 10.1002/macp.201300764
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An Organocatalytic Highly Enantioselective Stereospecific Synthesis of 1,1‐Disubstituted‐1,3‐Dihydroisobenzofurans.
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- Chemistry - A European Journal, 2024, v. 30, n. 25, p. 1, doi. 10.1002/chem.202303980
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Harnessing the Peterson Reaction for the Stereospecific Synthesis of Z‐Vinyl Ethers.
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- Chemistry - A European Journal, 2024, v. 30, n. 2, p. 1, doi. 10.1002/chem.202302708
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Alternating Stereospecificity upon Central‐Atom Change: Dynamics of the F<sup>−</sup>+PH<sub>2</sub>Cl S<sub>N</sub>2 Reaction Compared to its C‐ and N‐Centered Analogues.
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- Chemistry - A European Journal, 2023, v. 29, n. 58, p. 1, doi. 10.1002/chem.202302113
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Converging Stereodivergent Reactions: Highly Stereoselective Formal anti‐Markovnikov Addition of H<sub>2</sub>O to Mixtures of Olefins.
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- Chemistry - A European Journal, 2023, v. 29, n. 34, p. 1, doi. 10.1002/chem.202301031
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Stereospecific targeting of MTH1 by (S)-crizotinib as an anticancer strategy.
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- Nature, 2014, v. 508, n. 7495, p. 222, doi. 10.1038/nature13194
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Regio- and stereoselective synthesis of tetra- and triarylethenes by N-methylimidodiacetyl boron-directed palladium-catalysed three-component coupling.
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- Communications Chemistry, 2019, v. 2, n. 1, p. N.PAG, doi. 10.1038/s42004-019-0137-0
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Samarium-Mediated Asymmetric Synthesis.
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- Catalysts (2073-4344), 2023, v. 13, n. 1, p. 24, doi. 10.3390/catal13010024
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In Vivo, High-Throughput Selection of Thermostable Cyclohexanone Monooxygenase (CHMO).
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- Catalysts (2073-4344), 2020, v. 10, n. 8, p. 935, doi. 10.3390/catal10080935
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- Article
A novel carbonyl reductase with anti-Prelog stereospecificity for the production of t-butyl 6-cyano-(3R, 5R)-dihydroxyhexanoate.
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- 3 Biotech, 2019, v. 9, n. 5, p. N.PAG, doi. 10.1007/s13205-019-1722-8
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- Article
Accessing chiral sulfones bearing quaternary carbon stereocenters via photoinduced radical sulfur dioxide insertion and Truce–Smiles rearrangement.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-34836-y
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Copper-catalyzed Z-selective synthesis of acrylamides and polyacrylamides via alkylidene ketenimines.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-32082-w
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Cyclodextrins in Asymmetric and Stereospecific Synthesis.
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- Symmetry (20738994), 2015, v. 7, n. 4, p. 1699, doi. 10.3390/sym7041699
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Deammoniative Condensation of Primary Allylic Amines with Nonallylic Amines.
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- Chinese Journal of Chemistry, 2014, v. 32, n. 8, p. 741, doi. 10.1002/cjoc.201400406
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Stereoselective synthesis of new β-lactams from the main functional group of indomethacin.
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- Journal of the Iranian Chemical Society, 2022, v. 19, n. 6, p. 2475, doi. 10.1007/s13738-021-02466-8
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- Article
Catalytic Stability of S -1-(4-Hydroxyphenyl)-Ethanol Dehydrogenase from Aromatoleum aromaticum.
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- International Journal of Molecular Sciences, 2024, v. 25, n. 13, p. 7385, doi. 10.3390/ijms25137385
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- Article
Hydroperoxidation of Docosahexaenoic Acid by Human ALOX12 and pigALOX15-mini-LOX.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 7, p. 6064, doi. 10.3390/ijms24076064
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Polytopal Rearrangement Governing Stereochemistry of Bicyclic Oxime Ether Synthesis.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 20, p. 12331, doi. 10.3390/ijms232012331
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Insights to the Structural Basis for the Stereospecificity of the Escherichia coli Phytase, AppA.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 11, p. 6346, doi. 10.3390/ijms23116346
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Effects of Plant Oil Interesterified Triacylglycerols on Lipemia and Human Health.
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- International Journal of Molecular Sciences, 2018, v. 19, n. 1, p. 104, doi. 10.3390/ijms19010104
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Recombinant Lipase from Gibberella zeae Exhibits Broad Substrate Specificity: A Comparative Study on Emulsified and Monomolecular Substrate.
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- International Journal of Molecular Sciences, 2017, v. 18, n. 7, p. 1535, doi. 10.3390/ijms18071535
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Stereospecific Formal [3+2] Dipolar Cycloaddition of Cyclopropanes with Nitrosoarenes: An Approach to Isoxazolidines.
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- Angewandte Chemie, 2014, v. 126, n. 23, p. 6074, doi. 10.1002/ange.201400885
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Stereospecific Cyclic Poly(methyl methacrylate) and Its Topology-Guided Hierarchically Controlled Supramolecular Assemblies.
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- Angewandte Chemie, 2014, v. 126, n. 2, p. 469, doi. 10.1002/ange.201308366
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Regioselective and Stereospecific Deuteration of Bioactive Aza Compounds by the Use of Ruthenium Nanoparticles.
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- Angewandte Chemie, 2014, v. 126, n. 1, p. 234, doi. 10.1002/ange.201307930
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Stereospecific Biosynthesis of β-Methyltryptophan from L-Tryptophan Features a Stereochemical Switch.
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- Angewandte Chemie, 2013, v. 125, n. 49, p. 13189, doi. 10.1002/ange.201306255
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Chemical Diversification of Sialic Acid Glycosides by Stereospecific, Chemoselective Deamination.
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- Angewandte Chemie, 2013, v. 125, n. 43, p. 11549, doi. 10.1002/ange.201303781
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The Many Chemists Who Could Have Proposed the Woodward‐Hoffmann Rules But Didn't: The Organic Chemists Who Knew of the Smoking Guns.
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- Chemical Record, 2022, v. 22, n. 8, p. 1, doi. 10.1002/tcr.202200137
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- Article
The Many Chemists Who Could Have Proposed the Woodward‐Hoffmann Rules But Didn't: The Organic Chemists Who Discovered the Smoking Guns<sup>[</sup><sup>]</sup>**.
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- Chemical Record, 2022, v. 22, n. 6, p. 1, doi. 10.1002/tcr.202200065
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- Article
History of the Woodward‐Hoffmann Rules. The No‐Mechanism Puzzle**.
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- Chemical Record, 2022, v. 22, n. 2, p. 1, doi. 10.1002/tcr.202100212
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- Article
Stereospecificity in strigolactone biosynthesis and perception.
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- Planta: An International Journal of Plant Biology, 2016, v. 243, n. 6, p. 1361, doi. 10.1007/s00425-016-2523-5
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Theoretical Study of the Halogen Concentration Effect on the 1,3-Butadiene Polymerization Catalyzed by the Neodymium-Based Ziegler–Natta System.
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- Reactions (2624-781X), 2024, v. 5, n. 4, p. 753, doi. 10.3390/reactions5040037
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Synthesis and Properties of N,N′-Disubstituted Ureas and Their Isosteric Analogs Containing Polycyclic Fragments: XIX. exo-Isomers of N-(1,7,7-Trimethylbicyclo[2.2.1]heptan-2-yl)-N′-R-ureas and -thioureas.
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- Russian Journal of Organic Chemistry, 2024, v. 60, n. 3, p. 403, doi. 10.1134/S1070428024030059
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Synthesis and Properties of N,N′-Disubstituted Ureas and Their Isosteric Analogs Containing Polycyclic Fragments: IX. N-(1,7,7-Trimethylbicyclo[2.2.1]heptan-2-yl) Ureas and Thioureas.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 4, p. 515, doi. 10.1134/S1070428021040035
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Stereospecific Synthesis of cis-Verbenol.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 5, p. 755, doi. 10.1134/S1070428016050249
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- Article
Diastereospecific conjugation of 24-oxo-25,26,27-trinor analogs of ecdysteroids with L-ascorbic acid.
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- Russian Journal of Organic Chemistry, 2013, v. 49, n. 12, p. 1807, doi. 10.1134/S1070428013120166
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Professor Tien-Yau Luh: A Tribute.
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- ARKIVOC: Online Journal of Organic Chemistry, 2023, v. 2023, p. 1, doi. 10.24820/ark.5550190.p001.491
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An interesting sidetrack in the tofisopam synthesis: lithium variant of a stereospecific Oppenauer oxidation.
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- ARKIVOC: Online Journal of Organic Chemistry, 2015, v. 2015, p. 127, doi. 10.3998/ark.5550190.p008.964
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Protecting-group directed stereospecific organocatalytic [3+2] cycloadditions: a facile access to chiral spirocyclic oxindoles.
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- ARKIVOC: Online Journal of Organic Chemistry, 2014, p. 124
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Study of the stereospecificity in the biotransformation of the four isomers of loxoprofen sodium in rats by chiral HPLC.
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- Journal of Separation Science, 2024, v. 47, n. 1, p. 1, doi. 10.1002/jssc.202300562
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Rhodium-Catalyzed Asymmetric Allenylation of Sulfonylimines and Application to the Stereospecific Allylic Allenylation.
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- Advanced Synthesis & Catalysis, 2016, v. 358, n. 19, p. 3062, doi. 10.1002/adsc.201600686
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Enhancing the thermal and mechanical properties of PMMA using zinc carbazone complex as the initiator.
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- Journal of Thermal Analysis & Calorimetry, 2014, v. 115, n. 1, p. 707, doi. 10.1007/s10973-013-3317-7
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Stereospecific multiple isotopic labeling of benzyl alcohol.
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- Journal of Labelled Compounds & Radiopharmaceuticals, 2014, v. 57, n. 2, p. 75, doi. 10.1002/jlcr.3143
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Revisiting the 7-Phospanorbornene Family: New P-Alkyl Derivatives.
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- Heteroatom Chemistry, 2015, v. 26, n. 5, p. 335, doi. 10.1002/hc.21265
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- Article
Murine Alox8 versus the human ALOX15B ortholog: differences and similarities.
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- Pflügers Archiv: European Journal of Physiology, 2024, v. 476, n. 12, p. 1817, doi. 10.1007/s00424-024-02961-w
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On the mechanisms of protein interactions: predicting their affinity from unbound tertiary structures.
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- Bioinformatics, 2018, v. 34, n. 4, p. 592, doi. 10.1093/bioinformatics/btx616
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- Article
The crystal structure of a tetrahydrofolate-bound dihydrofolate reductase reveals the origin of slow product release.
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- Communications Biology, 2018, v. 1, n. 1, p. N.PAG, doi. 10.1038/s42003-018-0236-y
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- Article
Role of stereospecific nature of germinants in Bacillus megaterium spores germination.
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- 3 Biotech, 2017, v. 7, n. 4, p. 1, doi. 10.1007/s13205-017-0897-0
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- Article
Potent telomerase activators from a novel sapogenin via biotransformation utilizing Camarosporium laburnicola, an endophytic fungus.
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- Microbial Cell Factories, 2023, v. 22, n. 1, p. 1, doi. 10.1186/s12934-023-02069-3
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- Article
Synthesis of polypropylene/cellulosic fiber composites using Ziegler-Natta catalyst by in situ polymerization.
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- Polymer Engineering & Science, 2016, v. 56, n. 1, p. 71, doi. 10.1002/pen.24193
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