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1,2,5‐Triphenylpyrrole Derivatives with Dual Intense Photoluminescence in Both Solution and the Solid State: Solvatochromism and Polymorphic Luminescence Properties.
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- Chemistry - A European Journal, 2019, v. 25, n. 2, p. 573, doi. 10.1002/chem.201804074
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Noncatalytic Annulation of 4-Hydroxy-4-methylpent-2-ynenitrile to 3,3-Dimethyl-2-phenyl-3H-pyrrole. Stereoselective Synthesis of (Z)-2-(2,2,7,7-Tetramethyl-7a-phenyl-7,7a-dihydropyrrolo- [2,1-b]oxazol-3(2H)-ylidene)acetonitrile.
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- Russian Journal of Organic Chemistry, 2018, v. 54, n. 12, p. 1848, doi. 10.1134/S1070428018120217
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Vectorization of agrochemicals: amino acid carriers are more efficient than sugar carriers to translocate phenylpyrrole conjugates in the Ricinus system.
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- Environmental Science & Pollution Research, 2018, v. 25, n. 15, p. 14336, doi. 10.1007/s11356-016-8107-x
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- Article
Ethylene oligomerization over chromium(III) complexes with pyrrole derivatives.
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- Petroleum Chemistry, 2017, v. 57, n. 3, p. 244, doi. 10.1134/S0965544117010145
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- Article
Phenylpyrroles: 30 Years, Two Molecules and (Nearly) No Resistance.
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- Frontiers in Microbiology, 2016, v. 7, p. 1, doi. 10.3389/fmicb.2016.02014
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Dehydrogenation of 2-Phenyl-1-pyrroline with Palladium-Supported Catalysts: An Effective Route to the Synthesis of 2-Phenylpyrrole.
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- Catalysis Letters, 2015, v. 145, n. 3, p. 762, doi. 10.1007/s10562-014-1469-0
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- Article
Preparation and properties of co-oligomers of 1-vinyl-1,2,4-triazole with N-vinyl-2-phenylpyrrole.
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- Russian Journal of General Chemistry, 2015, v. 85, n. 2, p. 472, doi. 10.1134/S107036321502019X
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Synthesis of new, optically active 1-(substituted aryl)pyrrole derivatives via atropisomerism directed diastereoselective metalation.
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- ARKIVOC: Online Journal of Organic Chemistry, 2015, v. 2015, p. 80, doi. 10.3998/ark.5550190.p009.023
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Synthesis of polysubstituted pyrroles in aqueous medium directly from nitro compounds.
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- Russian Journal of General Chemistry, 2015, v. 85, n. 1, p. 155, doi. 10.1134/S1070363215010272
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Molecular and biochemical characterization of Sclerotinia sclerotiorum laboratory mutants resistant to dicarboximide and phenylpyrrole fungicides.
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- Journal of Pest Science, 2014, v. 87, n. 1, p. 221, doi. 10.1007/s10340-013-0526-6
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- Article
Synthesis and Antifungal Activity of Arylthiocyanates.
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- Pharmaceutical Chemistry Journal, 2013, v. 47, n. 8, p. 422, doi. 10.1007/s11094-013-0973-7
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- Article
Palladium-Catalysed Direct Polyarylation of Pyrrole Derivatives.
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- ChemCatChem, 2013, v. 5, n. 1, p. 255, doi. 10.1002/cctc.201200521
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- Article
Functional and Structural Comparison of Pyrrolnitrinand Iprodione-Induced Modifications in the Class III Histidine-Kinase Bos1 of Botrytis cinerea.
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- PLoS ONE, 2012, v. 7, n. 8, p. 1, doi. 10.1371/journal.pone.0042520
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The Group III Two-Component Histidine Kinase AlHK1 is Involved in Fungicides Resistance, Osmosensitivity, Spore Production and Impacts Negatively Pathogenicity in Alternaria longipes.
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- Current Microbiology, 2012, v. 64, n. 5, p. 449, doi. 10.1007/s00284-012-0093-8
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2-Phenylpyrrole: one-pot selective synthesis from acetophenone oxime and acetylene by a Trofimov reaction*.
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- Chemistry of Heterocyclic Compounds, 2012, v. 47, n. 11, p. 1367, doi. 10.1007/s10593-012-0922-5
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