Works matching DE "AMINO alcohols"
Results: 550
Constitutive Synthesis of Enzymes Involved in 2-Aminophenol Metabolism and Inducible Synthesis of Enzymes Involved in Benzoate, p-Hydroxybenzoate, and Protocatechuate Metabolism in Pseudomonas sp. Strain AP-3.
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- Bioscience, Biotechnology & Biochemistry, 2005, v. 69, n. 5, p. 1033, doi. 10.1271/bbb.69.1033
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Determination of the Absolute Configuration of (+)-Xestoaminol C [(2S, 3R)-2-Amino-3-tetradecanol], a Metabolite of Fiji Sponge, Xestospongia, sp., by the Synthesis of Its N,O-Diacetyl Derivative.
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- Bioscience, Biotechnology & Biochemistry, 2003, v. 67, n. 2, p. 329, doi. 10.1271/bbb.67.329
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Designing Cobalt(II) Complex for Chemoselective Synthesis of 2‐Aryl‐3‐Formyl Indoles from Amino Alcohols and Alcohols<sup>†</sup>.
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- Chemistry - A European Journal, 2024, v. 30, n. 47, p. 1, doi. 10.1002/chem.202401698
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Chiral NHC Ligands for Enantioselective Gold(I) Catalysis Under Aerobic Conditions: the Importance of Conformational Flexibility and Steric Hindrance of NHC Ligand on Reactivity.
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- Chemistry - A European Journal, 2024, v. 30, n. 13, p. 1, doi. 10.1002/chem.202303241
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Heterocyclic Merging of Stereochemically Diverse Chiral Piperazines and Morpholines with Indazoles.
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- Chemistry - A European Journal, 2023, v. 29, n. 55, p. 1, doi. 10.1002/chem.202301888
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One-Pot Synthesis of Chiral 1-Aryl-2-Aminoethanols via Ir-Catalyzed Asymmetric Hydrogenation.
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- Chemistry - A European Journal, 2023, v. 29, n. 29, p. 1, doi. 10.1002/chem.202300367
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Styrene Oxide Isomerase‐Catalyzed Meinwald Rearrangement in Cascade Biotransformations: Synthesis of Chiral and/or Natural Chemicals.
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- Chemistry - A European Journal, 2023, v. 29, n. 25, p. 1, doi. 10.1002/chem.202300102
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Supramolecular Architecture of an Amphiphilic Amino Alcohol as a Versatile Chiral Environment for Stereocontrolled Photoreaction of Various Anthracenes.
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- Chemistry - A European Journal, 2022, v. 28, n. 62, p. 1, doi. 10.1002/chem.202201940
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Photochemical Synthesis of the Bioactive Fragment of Salbutamol and Derivatives in a Self‐Optimizing Flow Chemistry Platform.
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- Chemistry - A European Journal, 2022, v. 28, n. 43, p. 1, doi. 10.1002/chem.202201385
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Asymmetric 1,2‐Migration at Vicinal Tetrasubstituted Stereocenters Constructed from α‐Keto Imines.
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- Angewandte Chemie, 2024, v. 136, n. 30, p. 1, doi. 10.1002/ange.202405212
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Unlocking the Asymmetric Hydrogenation of Tetrasubstituted Acyclic Enones.
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- Angewandte Chemie, 2024, v. 136, n. 9, p. 1, doi. 10.1002/ange.202315872
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Rhodium‐Catalyzed Enantioselective 1,4‐Oxyamination of Conjugated gem‐Difluorodienes via Coupling with Carboxylic Acids and Dioxazolones.
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- Angewandte Chemie, 2023, v. 135, n. 37, p. 1, doi. 10.1002/ange.202305669
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Nickel‐Catalyzed Chemoselective Arylation of Amino Alcohols.
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- Angewandte Chemie, 2023, v. 135, n. 23, p. 1, doi. 10.1002/ange.202300686
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Enforced Electronic‐Donor‐Acceptor Complex Formation in Water for Photochemical Cross‐Coupling.
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- Angewandte Chemie, 2023, v. 135, n. 17, p. 1, doi. 10.1002/ange.202218775
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Engineering Enzyme Substrate Scope Complementarity for Promiscuous Cascade Synthesis of 1,2‐Amino Alcohols.
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- Angewandte Chemie, 2022, v. 134, n. 46, p. 1, doi. 10.1002/ange.202212637
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The Rational Design and Atroposelective Synthesis of Axially Chiral C2‐Arylpyrrole‐Derived Amino Alcohols.
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- Angewandte Chemie, 2022, v. 134, n. 36, p. 1, doi. 10.1002/ange.202207517
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One‐Step Biocatalytic Synthesis of Sustainable Surfactants by Selective Amide Bond Formation**.
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- Angewandte Chemie, 2022, v. 134, n. 30, p. 1, doi. 10.1002/ange.202205054
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Cobalt/Salox‐Catalyzed Enantioselective C−H Functionalization of Arylphosphinamides.
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- Angewandte Chemie, 2022, v. 134, n. 25, p. 1, doi. 10.1002/ange.202202892
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Catalytic Substrate‐Selective Silylation of Primary Alcohols via Remote Functional‐Group Discrimination.
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- Angewandte Chemie, 2022, v. 134, n. 18, p. 1, doi. 10.1002/ange.202114118
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Chiroptical Switching and Quantitative Chirality Sensing with (Pseudo)halogenated Quinones.
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- Angewandte Chemie, 2021, v. 133, n. 52, p. 27237, doi. 10.1002/ange.202111542
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Practical Chemoselective Acylation: Organocatalytic Chemodivergent Esterification and Amidation of Amino Alcohols with N‐Carbonylimidazoles.
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- Angewandte Chemie, 2021, v. 133, n. 42, p. 23000, doi. 10.1002/ange.202107438
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Chiral Arylated Amines via C−N Coupling of Chiral Amines with Aryl Bromides Promoted by Light.
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- Angewandte Chemie, 2021, v. 133, n. 39, p. 21706, doi. 10.1002/ange.202108587
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Fine‐Tuning of Chiral Microenvironments within Triple‐Stranded Helicates for Enhanced Enantioselectivity.
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- Angewandte Chemie, 2021, v. 133, n. 30, p. 16704, doi. 10.1002/ange.202104111
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Frontispiz: Enantiodivergent Kinetic Resolution of 1,1′‐Biaryl‐2,2′‐Diols and Amino Alcohols by Dipeptide‐Phosphonium Salt Catalysis Inspired by the Atherton–Todd Reaction.
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- Angewandte Chemie, 2021, v. 133, n. 27, p. 1, doi. 10.1002/ange.202182762
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Enantiodivergent Kinetic Resolution of 1,1′‐Biaryl‐2,2′‐Diols and Amino Alcohols by Dipeptide‐Phosphonium Salt Catalysis Inspired by the Atherton–Todd Reaction.
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- Angewandte Chemie, 2021, v. 133, n. 27, p. 15048, doi. 10.1002/ange.202102352
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Anti‐Markovnikov Hydroamination of Racemic Allylic Alcohols to Access Chiral γ‐Amino Alcohols.
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- Angewandte Chemie, 2020, v. 132, n. 49, p. 22143, doi. 10.1002/ange.202009754
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Quantitative Chirality and Concentration Sensing of Alcohols, Diols, Hydroxy Acids, Amines and Amino Alcohols using Chlorophosphite Sensors in a Relay Assay.
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- Angewandte Chemie, 2020, v. 132, n. 48, p. 21566, doi. 10.1002/ange.202005324
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Bin Tan.
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- Angewandte Chemie, 2020, v. 132, n. 47, p. 20926, doi. 10.1002/ange.202009286
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CO<sub>2</sub> Methanation via Amino Alcohol Relay Molecules Employing a Ruthenium Nanoparticle/Metal Organic Framework Catalyst.
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- Angewandte Chemie, 2020, v. 132, n. 38, p. 16513, doi. 10.1002/ange.202004618
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Chromium‐Catalyzed Alkylation of Amines by Alcohols.
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- Angewandte Chemie, 2020, v. 132, n. 29, p. 11887, doi. 10.1002/ange.202001704
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Secondary Amino Alcohols: Traceless Cleavable Linkers for Use in Affinity Capture and Release.
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- Angewandte Chemie, 2020, v. 132, n. 28, p. 11663, doi. 10.1002/ange.202003478
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Chiral‐Organotin‐Catalyzed Kinetic Resolution of Vicinal Amino Alcohols.
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- Angewandte Chemie, 2019, v. 131, n. 45, p. 16323, doi. 10.1002/ange.201909700
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Cations Controlling the Chiral Assembly of Luminescent Atomically Precise Copper(I) Clusters.
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- Angewandte Chemie, 2019, v. 131, n. 35, p. 12271, doi. 10.1002/ange.201906614
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Enantioselective Aminohydroxylation of Styrenyl Olefins Catalyzed by an Engineered Hemoprotein.
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- Angewandte Chemie, 2019, v. 131, n. 10, p. 3170, doi. 10.1002/ange.201812968
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Synthesis and Pharmacological Activity of Amino Alcohols of the Indole Series.
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- Pharmaceutical Chemistry Journal, 2013, v. 47, n. 3, p. 125, doi. 10.1007/s11094-013-0909-2
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New synthesis of ethambutol and related α,β-acetylenic amino alcohols.
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- Pharmaceutical Chemistry Journal, 2013, v. 46, n. 12, p. 730, doi. 10.1007/s11094-013-0880-y
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Antioxidant and antiradical properties of new amino-acid derivatives of aminoalcohols.
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- Pharmaceutical Chemistry Journal, 2010, v. 44, n. 8, p. 421, doi. 10.1007/s11094-010-0481-y
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COMPARISON OF MOLECULAR PACKINGS OF CRYSTAL STRUCTURES OF (1S,3S)- AND (1S,3R)-1-tert-BUTYL- 3-METHYL-1-PHENYL-1,3-DIHYDRO-2-BENZOFURAN.
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- Journal of Structural Chemistry, 2020, v. 61, n. 12, p. 1975, doi. 10.1134/S0022476620120161
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Theoretical Modeling of the Structure of N-[2-[(Hydroxyalkylimino)Methyl]Phenyl]-4-Methylbenzene-Sulfamides and Their Mono- and Binuclear Copper(II) Complexes.
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- Journal of Structural Chemistry, 2019, v. 60, n. 3, p. 365, doi. 10.1134/S002247661903003X
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Reductive Amination of Glycosyl Aldoses: Synthesis of N-Glycosylatedβ-Glycosyl Amino Alcohols and their Enzyme Inhibitory Effect#.
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- Journal of Carbohydrate Chemistry, 2004, v. 23, n. 8/9, p. 493, doi. 10.1081/CAR-200046779
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Asymmetric Henry reaction catalyzed by Cu(I)-based chiral amino alcohol complex.
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- Turkish Journal of Chemistry, 2013, v. 37, n. 6, p. 966, doi. 10.3906/kim-1210-62
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New isoxazolidinyl-based N-alkylethanolamines as new activators of human brain carbonic anhydrases.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2023, v. 38, n. 1, p. 1, doi. 10.1080/14756366.2022.2164574
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Activation of carbonic anhydrases from human brain by amino alcohol oxime ethers: towards human carbonic anhydrase VII selective activators.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2021, v. 36, n. 1, p. 48, doi. 10.1080/14756366.2020.1838501
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No evidence of cross-reaction between fepradinol and other phenylethanolamines.
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- Contact Dermatitis (01051873), 1997, v. 36, n. 3, p. 170, doi. 10.1111/j.1600-0536.1997.tb00410.x
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Allergic contact dermatitis from mono-, di- and triethanolamine.
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- Contact Dermatitis (01051873), 1997, v. 36, n. 3, p. 166, doi. 10.1111/j.1600-0536.1997.tb00406.x
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Contact dermatitis due to diisopropanolamine.
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- Contact Dermatitis (01051873), 1989, v. 21, n. 1, p. 56, doi. 10.1111/j.1600-0536.1989.tb04690.x
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Chemoenzymatic One-Pot Process for the Synthesis of Tetrahydroisoquinolines.
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- Catalysts (2073-4344), 2021, v. 11, n. 11, p. 1389, doi. 10.3390/catal11111389
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Asymmetric Henry Reaction of Nitromethane with Substituted Aldehydes Catalyzed by Novel In Situ Generated Chiral Bis(β-Amino Alcohol-Cu(OAc) 2 ·H 2 O Complex.
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- Catalysts (2073-4344), 2021, v. 11, n. 10, p. 1208, doi. 10.3390/catal11101208
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Heteroaromatic N-Oxides Modified with a Chiral Oxazoline Moiety, Synthesis and Catalytic Applications.
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- Catalysts (2073-4344), 2021, v. 11, n. 4, p. 444, doi. 10.3390/catal11040444
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Multi-Catalytic Route for the Synthesis of (S)-Tembamide.
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- Catalysts (2073-4344), 2019, v. 9, n. 10, p. 822, doi. 10.3390/catal9100822
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