Works matching DE "TETRAHYDROPYRANYL compounds"
Results: 120
One-Pot Multi-Component Synthesis and Solid State Structures of Functionally Rich Polyether Macrocycles.
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- Advanced Synthesis & Catalysis, 2013, v. 355, n. 16, p. 3161, doi. 10.1002/adsc.201300462
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Glycosylation of 6 α,12 β-dihydroxy-20 R,25-epoxydammaran-3-one.
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- Chemistry of Natural Compounds, 2014, v. 50, n. 5, p. 868, doi. 10.1007/s10600-014-1103-9
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Phytochemical investigation of Tabebuia palmeri.
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- Chemistry of Natural Compounds, 2014, v. 49, n. 6, p. 1039, doi. 10.1007/s10600-014-0818-y
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Synthesis of optically active macrolides with hydrazide fragments from tetrahydropyran and L-(+)-tartaric acid derivatives.
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- Chemistry of Natural Compounds, 2013, v. 49, n. 4, p. 691, doi. 10.1007/s10600-013-0708-8
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The Ritter reaction for the synthesis of heterocycles.
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 11, p. 1167, doi. 10.1007/s10593-018-2189-y
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Cyclization of 5-amino-1-aryl-1 H-pyrazole-4-carbonitriles with β-dicarbonyl compounds.
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 2, p. 207, doi. 10.1007/s10593-017-2041-9
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Transformations of tetrahydro-1,4-benzoxazepines and tetrahydro-1,4-benzothiazepines under the action of alkynes. First example of the synthesis of tetrahydro-1,4-benzothiazonine-6-carboxylate.
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- Chemistry of Heterocyclic Compounds, 2013, v. 49, n. 2, p. 331, doi. 10.1007/s10593-013-1251-z
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Synthesis, antimicrobial and anticonvulsant screening of small library of tetrahydro-2 H -thiopyran-4-yl based thiazoles and selenazoles.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, p. 24, doi. 10.1080/14756366.2016.1186020
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The versatile low-molecular-weight thiols: Beyond cell protection.
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- BioEssays, 2015, v. 37, n. 12, p. 1262, doi. 10.1002/bies.201500067
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Synthesis of tetrahydropyridines by one-pot multicomponent reaction using nano-sphere silica sulfuric acid.
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- Journal of the Iranian Chemical Society, 2015, v. 12, n. 5, p. 855, doi. 10.1007/s13738-014-0548-x
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Stereoselective Synthesis of 1,2‐Annulated Sugars Having Substituted Tetrahydropyran/(‐furan) Scaffolds Using the Prins‐Reaction.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 47, p. 6706, doi. 10.1002/ejoc.201801273
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A General Approach to Various Five‐ and Six‐Membered gem‐Difluoroheterocycles: Application to the Synthesis of Fluorinated Analogues of Sedamine.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 27/28, p. 3782, doi. 10.1002/ejoc.201800371
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Recent Advances in Prins Spirocyclization.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 37, p. 5484, doi. 10.1002/ejoc.201700633
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Regio- and Stereoselective Synthesis of Acetallic Tetrahydropyrans as Building Blocks for Natural Products Preparation, via a Tandem [4+3]-Cycloaddition/Ozonolysis Process.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 27, p. 4674, doi. 10.1002/ejoc.201600590
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Introduction of Ether Groups onto Electron-Deficient Nitrogen-Containing Heteroaromatics Using Radical Chemistry under Transition-Metal-Free Conditions.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 22, p. 4973, doi. 10.1002/ejoc.201500584
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One-Pot Transformation of Simple Furans into Octahydroindole Scaffolds.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 14, p. 4020, doi. 10.1002/anie.201700620
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Tandem Allylboration-Prins Reaction for the Rapid Construction of Substituted Tetrahydropyrans: Application to the Total Synthesis of (−)-Clavosolide A.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 7, p. 2498, doi. 10.1002/anie.201511140
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Formation of the Δ<sup>18,19</sup> Double Bond and Bis(spiroacetal) in Salinomycin Is Atypically Catalyzed by SlnM, a Methyltransferase-like Enzyme.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 31, p. 9097, doi. 10.1002/anie.201503561
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Crystal structure of 6-(2-bromoacetamido)tetrahydro-2H-pyran-2,3,4,5-Tetrayl tetraacetate, C<sub>16</sub>H<sub>22</sub>BrNO<sub>10</sub>.
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- Zeitschrift für Kristallographie / New Crystal Structures, 2018, v. 233, n. 5, p. 955, doi. 10.1515/ncrs-2018-0158
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Synthesis and Antibacterial Activity of Oxalates and Acetamides of {2-[2-Sopropyltetrahydropyran-4-yl-4-(4-Fluorophenyl)]Ethyl}Arylamines.
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- Pharmaceutical Chemistry Journal, 2013, v. 47, n. 9, p. 490, doi. 10.1007/s11094-013-0987-1
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Eleuthesides and their analogs: V. Medium- and large-ring lactones based on levoglucosenone.
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- Russian Journal of Organic Chemistry, 2014, v. 50, n. 1, p. 117, doi. 10.1134/S1070428014010229
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Electrophilic intramolecular cyclization of functional derivatives of unsaturated compounds: IV. Cyclosulfenylation of 5-hexenoic acid amides and nucleophilic cleavage of reaction products.
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- Russian Journal of Organic Chemistry, 2013, v. 49, n. 8, p. 1168, doi. 10.1134/S1070428013080125
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Graphical Abstract: Asian J. Org. Chem. 7/2014.
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- Asian Journal of Organic Chemistry, 2014, v. 3, n. 7, p. 737, doi. 10.1002/ajoc.201490015
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- Article
An Efficient Stereoselective Synthesis of cis -2,6-Disubstituted Tetrahydropyrans via Gold-Catalyzed Meyer–Schuster Rearrangement/Hydration/ oxa -Michael Addition Sequence.
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- Catalysts (2073-4344), 2024, v. 14, n. 4, p. 228, doi. 10.3390/catal14040228
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Synthesis of Tetrahydropyran from Tetrahydrofurfuryl Alcohol over Cu-Zno/Al<sub>2</sub>O<sub>3</sub> under a Gaseous-Phase Condition.
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- Catalysts (2073-4344), 2018, v. 8, n. 3, p. 105, doi. 10.3390/catal8030105
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Osteogenic/Odontogenic Bioengineering with co-Administration of Simvastatin and Hydroxyapatite on Poly Caprolactone Based Nanofibrous Scaffold.
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- Advanced Pharmaceutical Bulletin, 2016, v. 6, n. 3, p. 353, doi. 10.15171/apb.2016.047
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Therapeutic effects of paeonol on methyl-4-phenyl-1,2,3,6-tetrahydropyridine/probenecid-induced Parkinson's disease in mice.
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- Molecular Medicine Reports, 2016, v. 14, n. 3, p. 2397, doi. 10.3892/mmr.2016.5573
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Toward Pyridine-Heterocycle Patterns through Prins and Aza-Prins Cyclisations: Application to a Short Synthesis of (±)-Anabasine.
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- European Journal of Organic Chemistry, 2014, v. 2014, n. 31, p. 7000, doi. 10.1002/ejoc.201402971
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Synthesis of the Spiroketal Fragment of (-)-Ushikulide A.
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- European Journal of Organic Chemistry, 2014, v. 2014, n. 25, p. 5574, doi. 10.1002/ejoc.201402196
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Cytotoxic and Antimicrobial Napyradiomycins from Two Marine-Derived Streptomyces Strains.
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- European Journal of Organic Chemistry, 2013, v. 2013, n. 18, p. 3751, doi. 10.1002/ejoc.201300349
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Effects of Neonatal Enzyme Replacement Therapy and Simvastatin Treatment on Cervical Spine Disease in Mucopolysaccharidosis I Dogs.
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- Journal of Bone & Mineral Research, 2014, v. 29, n. 12, p. 2610, doi. 10.1002/jbmr.2290
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1,8-Diazabicyclo[5.4.0]undec-7-ene: A Highly Efficient Catalyst for.
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- Journal of Heterocyclic Chemistry, 2014, v. 51, n. 3, p. 618, doi. 10.1002/jhet.1507
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Synthesis of complex oxygenated heterocycles.
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- Pure & Applied Chemistry, 2013, v. 85, n. 6, p. 1203, doi. 10.1351/PAC-CON-12-09-15
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Acid-washed bentonite: a new reagent for the deprotection of tetrahydropyranyl ethers.
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- Journal of Chemical Research, 2011, v. 35, n. 8, p. 477, doi. 10.3184/174751911X13103888466639
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Dissolution medium responsive simvastatin release from biodegradable apatite cements and the therapeutic effect in osteoporosis rats.
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- Journal of Applied Biomaterials & Functional Materials, 2012, v. 10, n. 1, p. 22, doi. 10.5301/JABFM.2012.9272
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Mucuna pruriens Protects against MPTP Intoxicated Neuroinflammation in parkinson's Disease through NF-κB/pAKT Signaling Pathways.
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- Frontiers in Aging Neuroscience, 2017, p. 1, doi. 10.3389/fnagi.2017.00421
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S-nitrosomycothiol reductase and mycothiol are required for survival under aldehyde stress and biofilm formation in Mycobacterium smegmatis.
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- IUBMB Life, 2016, v. 68, n. 8, p. 621, doi. 10.1002/iub.1524
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Tetrahydropyranyl protection and deprotection of alcohols using a niobium-based Brønsted acid catalyst.
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- Canadian Journal of Chemistry, 2016, v. 94, n. 8, p. 712, doi. 10.1139/cjc-2015-0538
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Investigation of Prins reaction for the synthesis of 2, 4- disubstituted tetrahydropyran derivatives and 1, 3-dioxanes using polyaniline supported acid as reusable catalyst.
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- Journal of Chemical Sciences, 2011, v. 123, n. 5, p. 623, doi. 10.1007/s12039-011-0122-3
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N-Heterocyclic Carbene Ligand-Enabled C(sp<sup>3</sup>)−H Arylation of Piperidine and Tetrahydropyran Derivatives.
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- Chemistry - A European Journal, 2016, v. 22, n. 14, p. 4748, doi. 10.1002/chem.201600191
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Stereoselective Synthesis and Physicochemical Properties of Liquid-Crystal Compounds Possessing a trans-2,5-Disubstituted Tetrahydropyran Ring with Negative Dielectric Anisotropy.
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- Chemistry - A European Journal, 2015, v. 21, n. 6, p. 2458, doi. 10.1002/chem.201405495
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Facile Access to cis-2,6-Disubstituted Tetrahydropyrans by Palladium-Catalyzed Decarboxylative Allylation: Total Syntheses of (±)-Centrolobine and (+)-Decytospolides A and B.
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- Chemistry - A European Journal, 2014, v. 20, n. 2, p. 405, doi. 10.1002/chem.201303328
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Synthesis and Biological Activity of 7,8,9-Trideoxy- and 7 R DesTHP-Peloruside A.
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- Chemistry - A European Journal, 2013, v. 19, n. 39, p. 13105, doi. 10.1002/chem.201301796
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A Dioxane Template for Highly Selective Epoxy Alcohol Cyclizations.
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- Chemistry - A European Journal, 2013, v. 19, n. 30, p. 10004, doi. 10.1002/chem.201300845
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Front Matter.
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- Chemistry - A European Journal, 2013, v. 19, n. 28, p. -1
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- Article
Co-Amorphous Simvastatin-Nifedipine with Enhanced Solubility for Possible Use in Combination Therapy of Hypertension and Hypercholesterolemia.
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- Molecules, 2018, v. 23, n. 9, p. 2161, doi. 10.3390/molecules23092161
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Metabolic and evolutionary origin of actin-binding polyketides from diverse organisms.
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- Nature Chemical Biology, 2015, v. 11, n. 9, p. 705, doi. 10.1038/nchembio.1870
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Redox Reorganization: Aluminium Promoted 1,5‐Hydride Shifts Allow the Controlled Synthesis of Multisubstituted Cyclohexenes.
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- Angewandte Chemie, 2023, v. 135, n. 36, p. 1, doi. 10.1002/ange.202307424
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The List–Varnek Collaboration at the Institute of Chemical Reaction Design and Discovery (ICReDD).
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- Angewandte Chemie, 2023, v. 135, n. 33, p. 1, doi. 10.1002/ange.202306925
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- Article
Frontispiz: Tandem Macrolactone Synthesis: Total Synthesis of (−)‐Exiguolide by a Macrocyclization/Transannular Pyran Cyclization Strategy.
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- Angewandte Chemie, 2022, v. 134, n. 22, p. 1, doi. 10.1002/ange.202282262
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