Works matching Carboxylic Acids
Results: 5000
Deoxyfluorination of Carboxylic, Sulfonic, Phosphinic Acids and Phosphine Oxides by Perfluoroalkyl Ether Carboxylic Acids Featuring CF<sub>2</sub>O Units.
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- Chinese Journal of Chemistry, 2021, v. 39, n. 5, p. 1225, doi. 10.1002/cjoc.202000662
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Boron Catalysis in the Transformation of Carboxylic Acids and Carboxylic Acid Derivatives.
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- European Journal of Organic Chemistry, 2023, v. 26, n. 1, p. 1, doi. 10.1002/ejoc.202201249
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Orthoamide und Iminiumsalze, CVIII. Umsetzungen von Orthoamiden der Alkincarbonsäuren mit CH/NH-aciden, tautomeriefähigen Verbindungen.
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- Zeitschrift für Naturforschung B: A Journal of Chemical Sciences, 2023, v. 78, n. 5, p. 307, doi. 10.1515/znb-2022-0113
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Orthoamide und Iminiumsalze, CV. Umsetzungen von Orthoamiden der Alkincarbonsäuren mit Carbonsäureamiden.
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- Zeitschrift für Naturforschung B: A Journal of Chemical Sciences, 2022, v. 77, n. 7/8, p. 565, doi. 10.1515/znb-2021-0096
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Mild and Efficient Synthesis of Carboxylic Acid Anhydrides from Carboxylic Acids and Triazine Coupling Reagents.
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- Synthetic Communications, 2004, v. 34, n. 18, p. 3349, doi. 10.1081/SCC-200030581
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Nickel‐Catalyzed Highly Selective Radical C−C Coupling from Carboxylic Acids with Photoredox Catalysis.
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- Angewandte Chemie, 2024, v. 136, n. 32, p. 1, doi. 10.1002/ange.202405866
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P450 酶活性中心催化全氟烷基羧酸前体化合物的代 谢转化路径研究.
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- Asian Journals of Ecotoxicology, 2023, v. 18, n. 3, p. 54, doi. 10.7524/AJE.1673-5897.20230202001
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Micellar Mediated Halodecarboxylation of α,β-Unsaturated Aliphatic and Aromatic Carboxylic Acids - A Novel Green Hunsdiecker-Borodin Reaction.
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- Journal of Dispersion Science & Technology, 2007, v. 28, n. 4, p. 613, doi. 10.1080/01932690701282690
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Decarboxylative and Decarbonylative Borylation of Carboxylic Acids and Their Derivatives<sup>†</sup>.
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- Chinese Journal of Chemistry, 2024, v. 42, n. 24, p. 3429, doi. 10.1002/cjoc.202400616
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Catalytic Synthesis of Phthalide Derivatives via Asymmetric Bromolactonization of Stilbene‐type Carboxylic Acids using N,N‐Dibenzyl Diaminomethylenemalononitrile as Organocatalyst.
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- Asian Journal of Organic Chemistry, 2023, v. 12, n. 7, p. 1, doi. 10.1002/ajoc.202300254
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Transition‐Metal‐Catalyzed Remote C(sp<sup>3</sup>)−H Functionalization Of Carboxylic Acid And Its Derivatives.
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- Asian Journal of Organic Chemistry, 2022, v. 11, n. 7, p. 1, doi. 10.1002/ajoc.202200184
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Nickel or Palladium‐Catalyzed Decarbonylative Transformations of Carboxylic Acid Derivatives.
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- Chemistry - An Asian Journal, 2020, v. 15, n. 8, p. 1234, doi. 10.1002/asia.202000117
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Substrate specificity for carnitine and glycine conjugation of branched side-chain and cyclic side-chain carboxylic acids in various experimental animals.
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- Xenobiotica, 2009, v. 39, n. 4, p. 335, doi. 10.1080/00498250902752187
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Ion Chromatography and Related Techniques in Carboxylic Acids Analysis.
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- Critical Reviews in Analytical Chemistry, 2021, v. 51, n. 6, p. 549, doi. 10.1080/10408347.2020.1750340
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Palladium‐Catalyzed Synthesis of Carboxylic Acid Anhydrides from Alkenes via in situ Generated Carboxylic Acids.
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- ChemCatChem, 2024, v. 16, n. 10, p. 1, doi. 10.1002/cctc.202301717
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Heterogeneously Catalyzed Carboxylic Acid Hydrogenation to Alcohols.
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- ChemCatChem, 2022, v. 14, n. 22, p. 1, doi. 10.1002/cctc.202200953
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Trends in Ozonation Disinfection By-Products—Occurrence, Analysis and Toxicity of Carboxylic Acids.
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- Water (20734441), 2020, v. 12, n. 3, p. 756, doi. 10.3390/w12030756
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Conceptual approach to the synthesis of symmetrical 1,3-diynes from β-bromo vinyl carboxylic acids.
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- Journal of Chemical Sciences, 2020, v. 132, n. 1, p. 1, doi. 10.1007/s12039-019-1693-7
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Gas chromatographic determination of some carboxylic acids: comparison between solution and headspace analysis.
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- Chemija, 2019, v. 30, n. 4, p. 227, doi. 10.6001/chemija.v30i4.4100
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Synthesis and Biological Activity of 2-(3,3-Dimethyl-6,7-Diethoxy-3,4-Dihydroisoquinolin-1-yl)Carboxylic Acid Hydrochlorides and Their Benzo[f]-Analogs.
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- Pharmaceutical Chemistry Journal, 2022, v. 56, n. 8, p. 1054, doi. 10.1007/s11094-022-02752-6
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Profiling of chiral and achiral carboxylic acid metabolomics: synthesis and evaluation of triazine-type chiral derivatization reagents for carboxylic acids by LC-ESI-MS/MS and the application to saliva of healthy volunteers and diabetic patients.
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- Analytical & Bioanalytical Chemistry, 2015, v. 407, n. 3, p. 1003, doi. 10.1007/s00216-014-8275-9
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Nickel‐Mediated Photoreductive Cross Coupling of Carboxylic Acid Derivatives for Ketone Synthesis**.
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- Chemistry - A European Journal, 2021, v. 27, n. 72, p. 18168, doi. 10.1002/chem.202103486
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Tertiary‐Amine‐Initiated Synthesis of Acyl Fluorides from Carboxylic Acids and CF<sub>3</sub>SO<sub>2</sub>OCF<sub>3</sub>.
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- Chemistry - A European Journal, 2020, v. 26, n. 69, p. 16261, doi. 10.1002/chem.202003756
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Bioactive carboxylic acids from Lysimachia clethroides.
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- Journal of Asian Natural Products Research, 2013, v. 15, n. 1, p. 59, doi. 10.1080/10286020.2012.745855
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Visible-Light-Mediated Dual Decarboxylative Coupling of Redox-Active Esters with α,β-Unsaturated Carboxylic Acids.
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- Chemistry - A European Journal, 2017, v. 23, n. 43, p. 10259, doi. 10.1002/chem.201702200
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ORGANOMETALLIC GAS‐PHASE ION CHEMISTRY AND CATALYSIS: INSIGHTS INTO THE USE OF METAL CATALYSTS TO PROMOTE SELECTIVITY IN THE REACTIONS OF CARBOXYLIC ACIDS AND THEIR DERIVATIVES.
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- Mass Spectrometry Reviews, 2021, v. 40, n. 6, p. 782, doi. 10.1002/mas.21654
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Polymer-Assisted Solution-Phase Synthesis Under Combined Ultrasound and Microwave Irradiation: Preparation of α,β-Unsaturated Esters and Carboxylic Acids, Key Intermediates of Novel Sigma Ligands.
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- Synthetic Communications, 2009, v. 39, n. 18, p. 3254, doi. 10.1080/00397910902738112
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Highly Efficient System for Reduction of Carboxylic Acids and Their Derivatives to Alcohols by HfCl4/KBH4.
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- Synthetic Communications, 2009, v. 39, n. 9, p. 1640, doi. 10.1080/00397910802573130
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Selective Esterification of Aliphatic Carboxylic Acids in the Presence of Aromatic Carboxylic Acids Over Monoammonium Salt of 12‐Tungstophosphoric Acid.
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- Synthetic Communications, 2006, v. 36, n. 1, p. 7, doi. 10.1080/00397910500328266
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Derivatives of biarylalkyl carboxylic acid induce pleiotropic phenotypes in adult Schistosoma mansoni in vitro.
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- Parasitology Research, 2016, v. 115, n. 10, p. 3831, doi. 10.1007/s00436-016-5146-7
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Synthesis and characterization of novel sulfur-containing 2-(1 H-pyrrolyl) carboxylic acids and their effects on garlic greening.
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- European Food Research & Technology, 2010, v. 231, n. 4, p. 555, doi. 10.1007/s00217-010-1306-7
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An Efficient Conversion of Carboxylic Acids to One-Carbon Degraded Aldehydes via 2-Hydroperoxy Acids.
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- Bioscience, Biotechnology & Biochemistry, 2007, v. 71, n. 5, p. 1370, doi. 10.1271/bbb.70105
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Investigation of eATRP for a Carboxylic‐Acid‐Functionalized Ionic Liquid Monomer.
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- Macromolecular Chemistry & Physics, 2021, v. 222, n. 4, p. 1, doi. 10.1002/macp.202000348
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Metal‐Free Ring‐Opening Alternating Copolymerization of Epoxides and Cyclic Anhydrides Mediated by a Ternary Phosphazene Base and Carboxylic Acids.
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- Macromolecular Chemistry & Physics, 2019, v. 220, n. 24, p. N.PAG, doi. 10.1002/macp.201900416
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Formal Transformation of Benzylic Carboxylic Acids to Phenols.
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- Chemistry - A European Journal, 2024, v. 30, n. 72, p. 1, doi. 10.1002/chem.202403301
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Cover Feature: Easy to Use DFT Approach for Computational pKa Determination of Carboxylic Acids (Chem. Eur. J. 1/2024).
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- Chemistry - A European Journal, 2024, v. 30, n. 1, p. 1, doi. 10.1002/chem.202303915
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Easy to Use DFT Approach for Computational pKa Determination of Carboxylic Acids.
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- Chemistry - A European Journal, 2024, v. 30, n. 1, p. 1, doi. 10.1002/chem.202303167
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Visible‐Light Enabled Dehydroxylative Alkylation of α‐Hydroxy Carboxylic Acid Derivatives via C−O Bond Cleavage.
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- Chemistry - A European Journal, 2023, v. 29, n. 57, p. 1, doi. 10.1002/chem.202302041
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Iron‐Catalyzed Deoxynitrogenation of Carboxylic Acids with Cyanamides to Access Nitriles.
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- Chemistry - A European Journal, 2023, v. 29, n. 31, p. 1, doi. 10.1002/chem.202300217
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Rh-Catalyzed Direct Decarbonylative Borylation of Carboxylic Acids.
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- Chemistry - A European Journal, 2023, v. 29, n. 29, p. 1, doi. 10.1002/chem.202300184
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Diastereo‐ and Enantioselective Reductive Mannich‐type Reaction of α,β‐Unsaturated Carboxylic Acids to Ketimines: A Direct Entry to Unprotected β<sup>2,3,3</sup>‐Amino Acids.
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- Chemistry - A European Journal, 2023, v. 29, n. 4, p. 1, doi. 10.1002/chem.202202575
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Ligand‐Promoted Rh<sup>I</sup>‐Catalyzed C2‐Selective C−H Alkenylation and Polyenylation of Imidazoles with Alkenyl Carboxylic Acids.
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- Chemistry - A European Journal, 2022, v. 28, n. 36, p. 1, doi. 10.1002/chem.202200441
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A General Iron‐Catalyzed Decarboxylative Oxygenation of Aliphatic Carboxylic Acids.
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- Angewandte Chemie, 2024, v. 136, n. 32, p. 1, doi. 10.1002/ange.202403292
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O‐Trifluoromethylation of Carboxylic Acids via the Formation and Activation of Acyloxy(phenyl)trifluoromethyl‐λ<sup>3</sup>‐Iodanes.
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- Angewandte Chemie, 2024, v. 136, n. 16, p. 1, doi. 10.1002/ange.202400449
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β‐ and γ‐C(sp<sup>3</sup>)−H Heteroarylation of Free Carboxylic Acids: A Modular Synthetic Platform for Diverse Quaternary Carbon Centers.
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- Angewandte Chemie, 2023, v. 135, n. 9, p. 1, doi. 10.1002/ange.202214459
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Triflylpyridinium Enables Rapid and Scalable Controlled Reduction of Carboxylic Acids to Aldehydes using Pinacolborane.
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- Angewandte Chemie, 2023, v. 135, n. 2, p. 1, doi. 10.1002/ange.202215168
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Selective Cross‐Ketonization of Carboxylic Acids Enabled by Metallaphotoredox Catalysis.
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- Angewandte Chemie, 2022, v. 134, n. 52, p. 1, doi. 10.1002/ange.202213739
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Titelbild: Decarboxylative Sulfinylation Enables a Direct, Metal‐Free Access to Sulfoxides from Carboxylic Acids (Angew. Chem. 43/2022).
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- Angewandte Chemie, 2022, v. 134, n. 43, p. 1, doi. 10.1002/ange.202284341
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Decarboxylative Sulfinylation Enables a Direct, Metal‐Free Access to Sulfoxides from Carboxylic Acids.
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- Angewandte Chemie, 2022, v. 134, n. 43, p. 1, doi. 10.1002/ange.202210525
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Deoxygenative Functionalizations of Aldehydes, Ketones and Carboxylic Acids.
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- Angewandte Chemie, 2022, v. 134, n. 10, p. 1, doi. 10.1002/ange.202112770
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