Works about PYRROLES
Results: 2362
Concise Total Synthesis of Acortatarin A.
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- Bioscience, Biotechnology & Biochemistry, 2013, v. 77, n. 3, p. 676, doi. 10.1271/bbb.120862
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Characterization and Functional Modification of StaC and RebC, Which Are Involved in the Pyrrole Oxidation of Indolocarbazole Biosynthesis.
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- Bioscience, Biotechnology & Biochemistry, 2011, v. 75, n. 11, p. 2184, doi. 10.1271/bbb.110474
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Synthesis of Lipid Derivatives of Pyrrole Polyamide and Their Biological Activity.
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- Bioscience, Biotechnology & Biochemistry, 2007, v. 71, n. 4, p. 1078, doi. 10.1271/bbb.60650
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Biosynthesis of the Marine Antibiotic Pentabromopseudilin. 2. The Pyrrole Ring.
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- Bioscience, Biotechnology & Biochemistry, 2005, v. 69, n. 3, p. 628, doi. 10.1271/bbb.69.628
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Synthesis and Insectidal Activity of Novel N-Oxydihydropyrrole Derivatives with a Substituted Spirocyclohexyl Group.
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- Bioscience, Biotechnology & Biochemistry, 2003, v. 67, n. 6, p. 1230, doi. 10.1271/bbb.67.1230
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Polypyrrole-Coated Jute Substrate for Electromagnetic Shielding.
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- AATCC Review, 2015, p. 54, doi. 10.14504/ajr.2.1.2
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Semi‐Crystalline Polypyrrole with Enhanced Electrochemical Properties Enabled by Air–Water Interface Confined Polymerization.
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- Macromolecular Chemistry & Physics, 2022, v. 223, n. 14, p. 1, doi. 10.1002/macp.202200026
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Cover Feature: Unveiling the Ultrafast Excitation Energy Transfer in Tetraarylpyrrolo[3,2‐b]pyrrole‐BODIPY Dyads (Chem. Eur. J. 71/2024).
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- Chemistry - A European Journal, 2024, v. 30, n. 71, p. 1, doi. 10.1002/chem.202487102
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Cover Feature: In Silico Design and Characterization of a New Molecular Electride: Li@Calix[3]Pyrrole (Chem. Eur. J. 38/2024).
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- Chemistry - A European Journal, 2024, v. 30, n. 38, p. 1, doi. 10.1002/chem.202401978
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In Silico Design and Characterization of a New Molecular Electride: Li@Calix[3]Pyrrole.
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- Chemistry - A European Journal, 2024, v. 30, n. 38, p. 1, doi. 10.1002/chem.202400448
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Palladium‐Catalyzed Carbonylation Reaction of Indole/Pyrrole Involving HCFO‐1233zd (E).
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- Chemistry - A European Journal, 2024, v. 30, n. 24, p. 1, doi. 10.1002/chem.202304056
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Binding of Acetylated Lysine by Using a Water Soluble Aryl Extended Calix[4]pyrrole.
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- Chemistry - A European Journal, 2024, v. 30, n. 18, p. 1, doi. 10.1002/chem.202303715
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Pyrrole <sup>β</sup>C−B−N Fused Porphyrins: Molecular Structures and Opto‐Electrochemical Studies.
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- Chemistry - A European Journal, 2024, v. 30, n. 17, p. 1, doi. 10.1002/chem.202304219
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Mn(II) Promoted Divergent‐Convergent Domino Reaction Giving Dinuclear Tetrasubstituted Pyrrole Complex.
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- Chemistry - A European Journal, 2024, v. 30, n. 17, p. 1, doi. 10.1002/chem.202303553
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Fluorogenic Rhodamine Probes with Pyrrole Substitution Enables STED and Lifetime Imaging of Lysosomes in Live Cells.
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- Chemistry - A European Journal, 2024, v. 30, n. 15, p. 1, doi. 10.1002/chem.202303707
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Intramolecular Carboxyamidation of Alkyne‐Tethered O‐Acylhydroxamates through Formation of Fe(III)‐Nitrenoids.
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- Chemistry - A European Journal, 2024, v. 30, n. 6, p. 1, doi. 10.1002/chem.202303428
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π‐Extended Hexapyrrolylbenzenes: Exploring Charge‐Transfer Phenomena in Donor‐Acceptor Propellers.
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- Chemistry - A European Journal, 2023, v. 29, n. 67, p. 1, doi. 10.1002/chem.202302429
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Diphenylpyrrole‐Strapped Calix[4]pyrrole Extractant for the Fluoride and Chloride Anions.
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- Chemistry - A European Journal, 2023, v. 29, n. 64, p. 1, doi. 10.1002/chem.202302410
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Cover Feature: Tunable Regioselectivity in C−H‐Activated Direct Arylation Reactions of Dithieno[3,2‐b:2',3'‐d]pyrroles (Chem. Eur. J. 60/2023).
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- Chemistry - A European Journal, 2023, v. 29, n. 60, p. 1, doi. 10.1002/chem.202303006
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Tunable Regioselectivity in C−H‐Activated Direct Arylation Reactions of Dithieno[3,2‐b:2',3'‐d]pyrroles.
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- Chemistry - A European Journal, 2023, v. 29, n. 60, p. 1, doi. 10.1002/chem.202301867
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A Versatile Route to Acyl (MIDA)Boronates.
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- Chemistry - A European Journal, 2023, v. 29, n. 58, p. 1, doi. 10.1002/chem.202302235
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2H‐Phosphindole‐Enabled Dearomatization and [4+2] Cycloaddition of (Hetero)Arenes.
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- Chemistry - A European Journal, 2023, v. 29, n. 54, p. 1, doi. 10.1002/chem.202301898
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Molecular Hinges by Fusion of Pyrrole and Dithiin: Synthesis, Structure, Redox Chemistry and Host–Guest Complexation of Dipyrrolo‐1,4‐dithiins.
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- Chemistry - A European Journal, 2023, v. 29, n. 27, p. 1, doi. 10.1002/chem.202300101
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Redox Assisted Reversible Aromaticity Transition Between 30π Hückel and 28π Möbius Dication of a Core‐Modified Isophlorinoid.
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- Chemistry - A European Journal, 2023, v. 29, n. 25, p. 1, doi. 10.1002/chem.202203327
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Diversification of Indoles and Pyrroles by Molecular Editing: New Frontiers in Heterocycle‐to‐Heterocycle Transmutation.
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- Chemistry - A European Journal, 2023, v. 29, n. 24, p. 1, doi. 10.1002/chem.202300096
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Tuning Directed Photooxidation‐Induced Conversion of Pyrrole‐Based Styryl Coumarin Dual‐Color Photoconverters.
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- Chemistry - A European Journal, 2023, v. 29, n. 20, p. 1, doi. 10.1002/chem.202203933
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Cover Feature: Plenates: Anion‐Dependent Self‐Assembly of the Pyrrole Cage Encapsulating Silver(I) Clusters (Chem. Eur. J. 12/2023).
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- Chemistry - A European Journal, 2023, v. 29, n. 12, p. 1, doi. 10.1002/chem.202300343
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Plenates: Anion‐Dependent Self‐Assembly of the Pyrrole Cage Encapsulating Silver(I) Clusters.
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- Chemistry - A European Journal, 2023, v. 29, n. 12, p. 1, doi. 10.1002/chem.202203850
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Synthesis of meso‐Free Decaphyrin(1.1.1.1.1.1.1.1.1.1) by a Hydrodebromination Protocol; Aromaticity and Solvent‐Polarity Dependent Conformational Change.
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- Chemistry - A European Journal, 2022, v. 28, n. 68, p. 1, doi. 10.1002/chem.202202682
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Access to Pyridinyl or Pyridinium Aza‐BODIPYs with Tunable Near‐Infrared Fluorescence through ICT from 4‐Pyridinyl Pyrroles**.
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- Chemistry - A European Journal, 2022, v. 28, n. 56, p. 1, doi. 10.1002/chem.202201503
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Aggregation Modes of Chiral Diketopyrrolo[3,4‐c]pyrrole Dyes in Solution and Thin Films.
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- Chemistry - A European Journal, 2022, v. 28, n. 51, p. 1, doi. 10.1002/chem.202201178
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Strain‐Induced Ring Expansion Reactions of Calix[3]pyrrole‐Related Macrocycles.
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- Chemistry - A European Journal, 2022, v. 28, n. 17, p. 1, doi. 10.1002/chem.202200056
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Unusual Regio‐ and Chemoselectivity in Oxidation of Pyrroles and Indoles Enabled by a Thianthrenium Salt Intermediate.
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- Angewandte Chemie, 2024, v. 136, n. 33, p. 1, doi. 10.1002/ange.202405057
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Cobalt‐Mediated Photochemical C−H Arylation of Pyrroles.
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- Angewandte Chemie, 2024, v. 136, n. 28, p. 1, doi. 10.1002/ange.202405780
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Controllable Skeletal and Peripheral Editing of Pyrroles with Vinylcarbenes.
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- Angewandte Chemie, 2024, v. 136, n. 24, p. 1, doi. 10.1002/ange.202401359
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Synthesis of Pyrrole‐Sharing Fused Porphyrinoid Hybrids by Post‐fabrication of Ni(II) Porphyrins.
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- Angewandte Chemie, 2024, v. 136, n. 8, p. 1, doi. 10.1002/ange.202319005
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One‐Carbon Ring Expansion of Indoles and Pyrroles: A Straightforward Access to 3‐Fluorinated Quinolines and Pyridines.
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- Angewandte Chemie, 2024, v. 136, n. 5, p. 1, doi. 10.1002/ange.202317104
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Synthesis of Closed‐Heterohelicenes Interconvertible between Their Monomeric and Dimeric Forms.
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- Angewandte Chemie, 2023, v. 135, n. 50, p. 1, doi. 10.1002/ange.202314968
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Total Synthesis of (−)‐Batrachotoxin Enabled by a Pd/Ag‐Promoted Suzuki–Miyaura Coupling Reaction.
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- Angewandte Chemie, 2023, v. 135, n. 40, p. 1, doi. 10.1002/ange.202309688
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Photochemically Mediated Ring Expansion of Indoles and Pyrroles with Chlorodiazirines: Synthetic Methodology and Thermal Hazard Assessment.
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- Angewandte Chemie, 2023, v. 135, n. 31, p. 1, doi. 10.1002/ange.202305081
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Bicyclo[1.1.1]pentane Embedded in Porphyrinoids**.
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- Angewandte Chemie, 2023, v. 135, n. 26, p. 1, doi. 10.1002/ange.202302771
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Enantioselective Synthesis of N‐N Atropisomers by Palladium‐Catalyzed C−H Functionalization of Pyrroles.
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- Angewandte Chemie, 2023, v. 135, n. 21, p. 1, doi. 10.1002/ange.202218871
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Chiral Calix[3]pyrrole Derivatives: Synthesis, Racemization Kinetics, and Ring Expansion to Calix[9]‐ and Calix[12]pyrrole Analogues.
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- Angewandte Chemie, 2023, v. 135, n. 15, p. 1, doi. 10.1002/ange.202301460
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Tuning Hole Transport Properties via Pyrrole Derivation for High‐Performance Perovskite Solar Cells.
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- Angewandte Chemie, 2023, v. 135, n. 15, p. 1, doi. 10.1002/ange.202300314
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Dual‐Color Photoconvertible Fluorescent Probes Based on Directed Photooxidation Induced Conversion for Bioimaging.
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- Angewandte Chemie, 2023, v. 135, n. 4, p. 1, doi. 10.1002/ange.202215085
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Antiaromatic Sapphyrin Isomer: Transformation into Contracted Porphyrinoids with Variable Aromaticity.
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- Angewandte Chemie, 2023, v. 135, n. 1, p. 1, doi. 10.1002/ange.202212174
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Synthesis of Subporphyrin Free Bases.
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- Angewandte Chemie, 2022, v. 134, n. 50, p. 1, doi. 10.1002/ange.202214342
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Chemical Investigations of Differentially Oxidized Polycylic Pyrroles from Bipolaris Fungi: Synthetic Entry Into the Bipolamine Alkaloids.
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- Angewandte Chemie, 2022, v. 134, n. 37, p. 1, doi. 10.1002/ange.202209457
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Frontispiz: Rhodium(I) Carbene‐Promoted Enantioselective C−H Functionalization of Simple Unprotected Indoles, Pyrroles and Heteroanalogues: New Mechanistic Insights.
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- Angewandte Chemie, 2022, v. 134, n. 34, p. 1, doi. 10.1002/ange.202283462
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Rhodium(I) Carbene‐Promoted Enantioselective C−H Functionalization of Simple Unprotected Indoles, Pyrroles and Heteroanalogues: New Mechanistic Insights.
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- Angewandte Chemie, 2022, v. 134, n. 34, p. 1, doi. 10.1002/ange.202207008
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