Works matching DE "ALLYL alcohol"
Results: 496
Oxidations of Allylic and Benzylic Alcohols under Inductively-Heated Flow Conditions with Gold-Doped Superparamagnetic Nanostructured Particles as Catalyst and Oxygen as Oxidant.
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- Advanced Synthesis & Catalysis, 2014, v. 356, n. 17, p. 3530, doi. 10.1002/adsc.201400261
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Catalytic Stereospecific Substitution of Enantioenriched Allylic Alcohols with Sodium Sulfinates.
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- Advanced Synthesis & Catalysis, 2014, v. 356, n. 14/15, p. 2984, doi. 10.1002/adsc.201400187
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Chemoselective Additions of Chloromethyllithium Carbenoid to Cyclic Enones: A Direct Access to Chloromethyl Allylic Alcohols.
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- Advanced Synthesis & Catalysis, 2014, v. 356, n. 8, p. 1761, doi. 10.1002/adsc.201301042
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Loss of function of the carbon catabolite repressor CreA leads to low but inducer‐independent expression from the feruloyl esterase B promoter in Aspergillus niger.
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- Biotechnology Letters, 2021, v. 43, n. 7, p. 1323, doi. 10.1007/s10529-021-03104-2
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Improved lycopene production by Blakeslea trispora with isopentenyl compounds and metabolic precursors.
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- Biotechnology Letters, 2012, v. 34, n. 5, p. 849, doi. 10.1007/s10529-011-0839-6
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Stereoselective Total Synthesis of Botryolide E.
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- Helvetica Chimica Acta, 2012, v. 95, n. 7, p. 1152, doi. 10.1002/hlca.201100512
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Reaction of isocembrol and alcohols on clay.
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- Chemistry of Natural Compounds, 2012, v. 48, n. 1, p. 56, doi. 10.1007/s10600-012-0158-8
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Novel synthetic approach to pyrrolo[1,2-b]cinnolines.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 8, p. 1030, doi. 10.1007/s10593-020-02770-w
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Synthesis of 1,3- and 1,2,3-functionalized pyrroles via Ir(I)-catalyzed vinylation of allyl alcohols.
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 5, p. 526, doi. 10.1007/s10593-017-2087-8
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Catalytic Alkylation of Furans by π-Activated Alcohols (Review).
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- Chemistry of Heterocyclic Compounds, 2014, v. 50, n. 6, p. 791, doi. 10.1007/s10593-014-1534-z
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Investigations into molecular interactions in binary mixtures of allyl alcohol and chlorinated methanes, along with the correlation analysis using FT-IR spectra and correlation with the Jouyban –Acree model.
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- Physics & Chemistry of Liquids, 2024, v. 62, n. 6, p. 651, doi. 10.1080/00319104.2024.2334848
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Study on the molecular interactions of binary mixtures of allyl alcohol with isomeric amyl alcohol solvents through thermodynamic properties and FT-IR spectra and correlation with the Jouyban–Acree model.
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- Physics & Chemistry of Liquids, 2024, v. 62, n. 5, p. 377, doi. 10.1080/00319104.2024.2310510
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Thermophysical properties of binary liquid mixtures at various temperatures, supported by FTIR spectral studies and correlation with the Jouyban–Acree model (allyl alcohol, benzyl aldehyde, benzylamine and benzyl alcohol).
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- Physics & Chemistry of Liquids, 2024, v. 62, n. 4, p. 229, doi. 10.1080/00319104.2023.2297210
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Mechanistic Understanding of Transition-Metal-Catalyzed Olefin Isomerization: Metal-Hydride Insertion-Elimination vs. π-Allyl Pathways.
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- Comments on Inorganic Chemistry, 2015, v. 35, n. 6, p. 301, doi. 10.1080/02603594.2015.1059325
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Bitkisel Yağlardan Polimerize Olabilen Monomerin Sentezi ve Fotopolimerleşmesi.
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- Journal of the Institute of Science & Technology / Iğdır Üniversitesi Fen Bilimleri Enstitüsü Dergisi, 2021, v. 11, n. 1, p. 393, doi. 10.21597/jist.746693
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Mn(I)-catalyzed sigmatropic rearrangement of β, γ-unsaturated alcohols.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-37299-x
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Mn(I)-catalyzed sigmatropic rearrangement of β, γ-unsaturated alcohols.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-37299-x
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Solid-Liquid Phase Transfer Catalyzed Selective Reduction of Bifunctional Moieties.
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- Orbital: The Electronic Journal of Chemistry, 2021, v. 13, n. 4, p. 269, doi. 10.17807/orbital.v13i4.1576
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UV-curable waterborne epoxy acrylate coating modified by monomethacryloyloxy-terminated fluorinated oligomer.
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- Journal of Coatings Technology & Research, 2019, v. 16, n. 5, p. 1305, doi. 10.1007/s11998-019-00209-2
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Synthesis and characterization of polyether-modified silicones.
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- Wool Textile Journal, 2020, v. 48, n. 9, p. 35, doi. 10.19333/j.mfkj.20191201905
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Palladium mediated domino heck redox cyclization of aromatic homoallylic alcohols to methylindanones.
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- Journal of the Iranian Chemical Society, 2024, v. 21, n. 8, p. 2259, doi. 10.1007/s13738-024-03053-3
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Barium manganate: a versatile oxidant in organic synthesis.
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- Journal of the Iranian Chemical Society, 2023, v. 20, n. 9, p. 2139, doi. 10.1007/s13738-023-02838-2
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Investigation of catalytic activity of vanadyl sulphate immobilized on prepared UiO-66 modified with urea and melamine as allyl alcohol epoxidation catalysts.
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- Journal of the Iranian Chemical Society, 2022, v. 19, n. 12, p. 4669, doi. 10.1007/s13738-022-02649-x
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Direct Nucleophilic Substitution of Alcohols Using an Immobilized Oxovanadium Catalyst.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 31, p. 4417, doi. 10.1002/ejoc.202100569
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ω‐Alkenylallylboronates: Design, Synthesis, and Application to the Asymmetric Allylation/RCM Tandem Sequence.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 24, p. 3492, doi. 10.1002/ejoc.202100528
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Synthesis of (+) and (‐)‐Streptomyces coelicolor Butanolide 5 (SCB‐5).
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 22, p. 3345, doi. 10.1002/ejoc.202100497
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ZnBr<sub>2</sub> Mediated C--N Bond Formation using Cinnamyl Alcohol and 2-Amino Pyridines.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 21, p. 3054, doi. 10.1002/ejoc.202100463
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The Chemistry of β-Hydroxy Hydroperoxides.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 21, p. 2990, doi. 10.1002/ejoc.202100343
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Selective Synthesis of 5-Alkylated and 5-Alkenylated Chromones via Catalytic C-H Coupling of Chromones with Allyl Alcohols.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 17, p. 2411, doi. 10.1002/ejoc.202100213
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Water‐Promoted Dehydrative Tsuji–Trost Reaction of Non‐Derivatized Allylic Alcohols with Sulfinic Acids.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 46, p. 7238, doi. 10.1002/ejoc.202001306
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Fluoroalkylation of Allylic Alcohols with Concomitant (Hetero)aryl Migration: Access to Fluoroalkylated Ketones and Evaluation of Antifungal Action against Magnaporthe grisea.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 32, p. 5192, doi. 10.1002/ejoc.202000782
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H‐*BEA Zeolite‐Catalyzed Nucleophilic Substitution in Allyl Alcohols Using Sulfonamides, Amides, and Anilines.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 28, p. 4309, doi. 10.1002/ejoc.202000296
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Regio‐ and Enantioselective Substrate‐Directed Epoxidation.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 16, p. 2369, doi. 10.1002/ejoc.201901656
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Copper‐Catalyzed Stereospecific Hydroboration of Internal Allylic Alcohols.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 44, p. 7367, doi. 10.1002/ejoc.201901435
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Halogenated Allyl Alcohol Derivatives ‐ Versatile Electrophiles for Palladium‐Catalyzed Allylic Alkylations.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 17, p. 2843, doi. 10.1002/ejoc.201900310
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KO tBu-Mediated Domino Isomerization and Functionalization of Aromatic Allylic Alcohols.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 26, p. 3886, doi. 10.1002/ejoc.201700440
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Diastereoselective Synthesis of trans-2,3-Diaryl(heteroaryl)-3,6-dihydropyrans by an Allylboration/Ring-Closing-Metathesis Sequence.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 23, p. 3343, doi. 10.1002/ejoc.201700448
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Flow Dehydration and Hydrogenation of Allylic Alcohols: Application to the Waste-Free Synthesis of Pristane.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 10, p. 1365, doi. 10.1002/ejoc.201700072
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A Metathesis Route to (+)-Orientalol F, a Guaiane Sesquiterpene from Alisma Orientalis.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 35, p. 5881, doi. 10.1002/ejoc.201601197
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Divergent Synthesis of Quinolone Natural Products from Pseudonocardia sp. CL38489.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 35, p. 5799, doi. 10.1002/ejoc.201601195
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Nickel(0)-Catalyzed N-Allylation of Amides and p-Toluenesulfonamide with Allylic Alcohols under Neat and Neutral Conditions.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 22, p. 3796, doi. 10.1002/ejoc.201600500
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A Formal Intermolecular Iodolactonization Reaction Based on a Radical-Ionic Sequence.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 9, p. 1739, doi. 10.1002/ejoc.201600051
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Nickel-Catalysed Bis-Allylation of Activated Nucleophiles with Allyl Alcohol.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 6, p. 1194, doi. 10.1002/ejoc.201501556
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Unexpected Mild Protection of Alcohols as 2- O-THF and 2- O-THP Ethers Catalysed by Cp<sub>2</sub>TiCl Reveal an Intriguing Role of the Solvent in the Single-Electron Transfer Reaction.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 28, p. 6333, doi. 10.1002/ejoc.201500869
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Characterization of Water/Sucrose Laurate/ n-Propanol/Allylbenzene Microemulsions.
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- Journal of Surfactants & Detergents, 2012, v. 15, n. 4, p. 505, doi. 10.1007/s11743-012-1344-1
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Enantioselective Dearomatization of Naphthol Derivatives with Allylic Alcohols by Cooperative Iridium and Brønsted Acid Catalysis.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 12, p. 3242, doi. 10.1002/anie.201609693
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Photoredox Activation of SF<sub>6</sub> for Fluorination.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 48, p. 15072, doi. 10.1002/anie.201608792
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Extremely Active Organocatalysts Enable a Highly Enantioselective Addition of Allyltrimethylsilane to Aldehydes.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 42, p. 13200, doi. 10.1002/anie.201607828
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From a Sequential to a Concurrent Reaction in Aqueous Medium: Ruthenium-Catalyzed Allylic Alcohol Isomerization and Asymmetric Bioreduction.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 30, p. 8691, doi. 10.1002/anie.201601840
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A Concise Route to the Strongylophorines.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 29, p. 8294, doi. 10.1002/anie.201602476
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