Works matching DE "SPIRO compounds"
Results: 334
Orthogonal Geometry Enhancing the Intersystem Crossing and Photosensitive Efficiency of Spiro Organoboron Compounds.
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- Chemistry - A European Journal, 2024, v. 30, n. 66, p. 1, doi. 10.1002/chem.202402606
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Synthesis and Characterization of a Cyclic Trimer of a Chiral Spirosilabifluorene.
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- Chemistry - A European Journal, 2024, v. 30, n. 45, p. 1, doi. 10.1002/chem.202401343
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Cover Feature: Synthesis of Highly Functionalized Spirocycles and Pentafulvene‐Containing Dyes Involving 2‐(2′‐ketoalkyl)‐1,3‐indandiones (Chem. Eur. J. 71/2023).
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- Chemistry - A European Journal, 2023, v. 29, n. 71, p. 1, doi. 10.1002/chem.202303811
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From Terminal to Spiro‐Phosphonium Acceptors, Remarkable Moieties to Develop Polyaromatic NIR Dyes.
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- Chemistry - A European Journal, 2023, v. 29, n. 44, p. 1, doi. 10.1002/chem.202301073
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Chiral NHC‐Catalyzed [4+2] Cycloadditions: Highly Diastereo/Enantioselective Access to Spiro[cyclohex‐4‐ene‐1,3′‐indoles] and DFT Calculations.
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- Chemistry - A European Journal, 2023, v. 29, n. 23, p. 1, doi. 10.1002/chem.202203818
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Development of TfOH‐Catalyzed Spirocyclization by Intramolecular Friedel‐Crafts‐type 1,4‐Addition: Application to the Total Synthesis of the Unusual Proaporphine Alkaloid (±)‐Misrametine.
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- Chemistry - A European Journal, 2022, v. 28, n. 60, p. 1, doi. 10.1002/chem.202202188
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Synthesis of 3‐Borylated Pyrrolidines by 1,3‐Dipolar Cycloaddition of Alkenyl Boronates and Azomethine Ylide.
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- Chemistry - A European Journal, 2022, v. 28, n. 54, p. 1, doi. 10.1002/chem.202202117
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Cover Feature: Synthesis of Spirocyclic Cyclobutenes through Desulfinative Spirocyclisation of gem‐Bis(triflyl)cyclobutenes (Chem. Eur. J. 33/2022).
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- Chemistry - A European Journal, 2022, v. 28, n. 33, p. 1, doi. 10.1002/chem.202201547
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Synthesis of Spirocyclic Cyclobutenes through Desulfinative Spirocyclisation of gem‐Bis(triflyl)cyclobutenes.
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- Chemistry - A European Journal, 2022, v. 28, n. 33, p. 1, doi. 10.1002/chem.202200704
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Spiroborate‐Based Host Materials with High Triplet Energies and Ambipolar Charge‐Transport Properties.
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- Angewandte Chemie, 2023, v. 135, n. 14, p. 1, doi. 10.1002/ange.202217512
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Electronic Control of the Scholl Reaction: Selective Synthesis of Spiro vs Helical Nanographenes.
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- Angewandte Chemie, 2023, v. 135, n. 7, p. 1, doi. 10.1002/ange.202215655
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Total Synthesis of Spiro[cyclohexane‐2‐indoline] Alkaloids: A Regio‐ and Diastereoselective Spirocyclization Approach.
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- Angewandte Chemie, 2022, v. 134, n. 49, p. 1, doi. 10.1002/ange.202212042
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Enantioselective Synthesis of Spirosilabicyclohexenes by Asymmetric Dual Ring Expansion of Spirosilabicyclobutane with Alkynes.
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- Angewandte Chemie, 2022, v. 134, n. 48, p. 1, doi. 10.1002/ange.202212889
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Electrophilic Spirocyclization of a 2‐Biphenylacetylene via Conformational Fixing within a Hollow‐Cage Host.
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- Angewandte Chemie, 2022, v. 134, n. 24, p. 1, doi. 10.1002/ange.202203970
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Strain‐Release‐Driven Friedel–Crafts Spirocyclization of Azabicyclo[1.1.0]butanes.
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- Angewandte Chemie, 2022, v. 134, n. 3, p. 1, doi. 10.1002/ange.202114235
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Enantio‐ and Diastereodivergent Synthesis of Spirocycles through Dual‐Metal‐Catalyzed [3+2] Annulation of 2‐Vinyloxiranes with Nucleophilic Dipoles.
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- Angewandte Chemie, 2021, v. 133, n. 47, p. 25145, doi. 10.1002/ange.202111842
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Carbene‐Stabilized Dithiolene (L<sup>0</sup>) Zwitterions.
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- Angewandte Chemie, 2021, v. 133, n. 42, p. 22888, doi. 10.1002/ange.202108498
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Dynamic Kinetic Asymmetric Transformation of Racemic Diastereomers: Diastereo‐ and Enantioconvergent Michael–Henry Reactions to Afford Spirooxindoles Bearing Furan‐Fused Rings.
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- Angewandte Chemie, 2021, v. 133, n. 39, p. 21426, doi. 10.1002/ange.202108734
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Enantioselective Synthesis of Spiro‐oxiranes: An Asymmetric Addition/Aldol/Spirocyclization Domino Cascade.
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- Angewandte Chemie, 2021, v. 133, n. 39, p. 21359, doi. 10.1002/ange.202105562
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Strain‐Release Driven Spirocyclization of Azabicyclo[1.1.0]butyl Ketones.
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- Angewandte Chemie, 2021, v. 133, n. 21, p. 11930, doi. 10.1002/ange.202102754
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A TADF Emitter Featuring Linearly Arranged Spiro‐Donor and Spiro‐Acceptor Groups: Efficient Nondoped and Doped Deep‐Blue OLEDs with CIE<sub>y</sub> <0.1.
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- Angewandte Chemie, 2021, v. 133, n. 17, p. 9684, doi. 10.1002/ange.202100423
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Asymmetric Dearomatization of Indole by Palladium/PC‐Phos‐Catalyzed Dynamic Kinetic Transformation.
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- Angewandte Chemie, 2020, v. 132, n. 49, p. 22175, doi. 10.1002/ange.202010164
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Engineering the Charge‐Transfer State to Facilitate Spin–Orbit Charge Transfer Intersystem Crossing in Spirobis[anthracene]diones.
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- Angewandte Chemie, 2020, v. 132, n. 49, p. 22363, doi. 10.1002/ange.202009439
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A Dearomatization/Debromination Strategy for the [4+1] Spiroannulation of Bromophenols with α,β‐Unsaturated Imines.
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- Angewandte Chemie, 2020, v. 132, n. 43, p. 19147, doi. 10.1002/ange.202008130
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Manipulation of Spiroindolenine Intermediates for Enantioselective Synthesis of 3‐(Indol‐3‐yl)‐Pyrrolidines.
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- Angewandte Chemie, 2019, v. 131, n. 4, p. 1170, doi. 10.1002/ange.201812344
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Synthesis and analgesic activity of 3,5-diaryl-2-oxaspiro[5,6]dodec-3-en-1-ones.
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- Pharmaceutical Chemistry Journal, 2013, v. 47, n. 1, p. 40, doi. 10.1007/s11094-013-0892-7
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Synthesis and Biological Activity of 3-Spiro[adamantane-2,3′-isoquinolines].
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- Pharmaceutical Chemistry Journal, 2013, v. 46, n. 12, p. 707, doi. 10.1007/s11094-013-0874-9
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Analgesic activity of 4-aryl-8(arylmethylene)-5,6,7,8-tetrahydrospiro[chromen-3,1'-cycloalkan]-2(4 H)-ones.
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- Pharmaceutical Chemistry Journal, 2012, v. 46, n. 5, p. 269, doi. 10.1007/s11094-012-0777-1
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Crystal structure of diethyl-1-isobutyl-9-hydroxy-9-methyl-7-phenyl-1,4-diazaspiro[4,5] decane-6,8-dicarboxylate CHNO.
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- Journal of Structural Chemistry, 2013, v. 54, n. 6, p. 1137, doi. 10.1134/S002247661306019X
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An efficient one-pot, three-component synthesis of 6-cyano-hexahydro-4 H-thieno[3',2':5,6]pyrimido[1,2- α]quinoline-2-carboxylates and their spiro derivatives from β-enaminones.
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- Turkish Journal of Chemistry, 2016, v. 40, n. 3, p. 434, doi. 10.3906/kim-1507-31
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Photovoltaics: Recent Advances in Spiro‐MeOTAD Hole Transport Material and Its Applications in Organic–Inorganic Halide Perovskite Solar Cells (Adv. Mater. Interfaces 1/2018).
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- Advanced Materials Interfaces, 2018, v. 5, n. 1, p. 1, doi. 10.1002/admi.201870003
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Recent Advances in Spiro‐MeOTAD Hole Transport Material and Its Applications in Organic–Inorganic Halide Perovskite Solar Cells.
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- Advanced Materials Interfaces, 2018, v. 5, n. 1, p. 1, doi. 10.1002/admi.201700623
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A Previously Unreported Shell Bead Type for Southern California and Eastern Arizona.
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- Central States Archaeological Journal, 2019, v. 66, n. 4, p. 185
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A Catalyst-Free One-Pot Multicomponent Green Strategy for the Synthesis of Spiroindene-1,3dione-Benzochromene/ Thio-Chromene Derivatives under Neat/Aqueous Conditions.
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- Polycyclic Aromatic Compounds, 2024, v. 44, n. 9, p. 5859, doi. 10.1080/10406638.2023.2270126
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Reactions of cyclochlorotriphosphazatriene with 1-amino-2-propanol. Calorimetric and spectroscopic investigations of the derived products.
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- Sakarya University Journal of Science (SAUJS) / Sakarya Üniversitesi Fen Bilimleri Enstitüsü Dergisi, 2018, v. 22, n. 3, p. 1033, doi. 10.16984/saufenbilder.384736
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Quantification of deoxynivalenol and fumonisins in cereals and derived products by high-performance liquid chromatography.
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- Journal of Food Safety & Food Quality / Archiv für Lebensmittelhygiene, 2021, v. 72, n. 3, p. 94, doi. 10.31083/0003-925x-72-94
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Purified deoxynivalenol or feed restriction reduces mortality in rainbow trout, Oncorhynchus mykiss (Walbaum), with experimental bacterial coldwater disease but biologically relevant concentrations of deoxynivalenol do not impair the growth of Flavobacterium psychrophilum
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- Journal of Fish Diseases, 2015, v. 38, n. 9, p. 809, doi. 10.1111/jfd.12295
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Investigation of Pharmaceutical Importance of 2 H -Pyran-2-One Analogues via Computational Approaches.
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- Symmetry (20738994), 2021, v. 13, n. 9, p. 1619, doi. 10.3390/sym13091619
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Regio- and Stereoselective Synthesis of a New Series of Spirooxindole Pyrrolidine Grafted Thiochromene Scaffolds as Potential Anticancer Agents.
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- Symmetry (20738994), 2021, v. 13, n. 8, p. 1426, doi. 10.3390/sym13081426
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DABCO-functionalized mesoporous SBA-15: an efficient and recyclable catalyst for the synthesis of spiro-pyranoxindoles as antioxidant agents.
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- Canadian Journal of Chemistry, 2014, v. 92, n. 12, p. 1163, doi. 10.1139/cjc-2014-0309
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Linearly Arranged Multi‐π‐Stacked Structure for Efficient Through‐Space Charge‐Transfer Emitters.
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- Angewandte Chemie, 2024, v. 136, n. 38, p. 1, doi. 10.1002/ange.202408712
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Macromolecular helicity induction and static helicity memory of poly(biphenylylacetylene)s bearing aromatic pendant groups and their use as chiral stationary phases for high‐performance liquid chromatography.
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- Chirality, 2022, v. 34, n. 2, p. 306, doi. 10.1002/chir.23399
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Synthetic approaches to [5,6]-benzannulated spiroketal natural products.
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- Pure & Applied Chemistry, 2012, v. 84, n. 6, p. 1379
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Reaction of [2-(3-hetaryl-1,2,4-triazol-5-yl)phenyl]amines with ketones: a density functional theory study.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2024, v. 143, n. 4, p. 1, doi. 10.1007/s00214-024-03110-3
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Subacute Cardiovascular Toxicity of the Marine Phycotoxin Azaspiracid-1 in Rats.
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- Toxicological Sciences, 2016, v. 151, n. 1, p. 104, doi. 10.1093/toxsci/kfw025
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Deoxynivalenol (Vomitoxin)-Induced Cholecystokinin and Glucagon-Like Peptide-1 Release in the STC-1 Enteroendocrine Cell Model Is Mediated by Calcium- Sensing Receptor and Transient Receptor Potential Ankyrin-1 Channel.
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- Toxicological Sciences, 2015, v. 145, n. 2, p. 407, doi. 10.1093/toxsci/kfv061
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Synthesis, Evaluation and Proposed Binding Pose of Substituted Spiro‐Oxindole Dihydroquinazolinones as IRAP Inhibitors.
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- ChemistryOpen, 2020, v. 9, n. 3, p. 325, doi. 10.1002/open.201900344
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Experimentally Validated Novel Factor XIIa Inhibitors Identified by Docking and Quantum Chemical Post‐processing.
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- Molecular Informatics, 2023, v. 42, n. 2, p. 1, doi. 10.1002/minf.202200205
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Derivation of Benzothiadiazine‐1,1‐dioxide Scaffolds via Transition Metal‐Catalyzed C—H Activation/Annulation.
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- Chinese Journal of Chemistry, 2023, v. 41, n. 16, p. 1973, doi. 10.1002/cjoc.202300095
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A novel one-pot three-component approach to 4-amino-functionalized spiropyrimidine-2-thiones.
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- Journal of the Iranian Chemical Society, 2019, v. 16, n. 6, p. 1139, doi. 10.1007/s13738-018-01589-9
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