Found: 18
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Enhanced Activity in the Tosylation of Tolanophanes via Supramolecular HgCl<sub>2</sub> Recognition.
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- Australian Journal of Chemistry, 2020, v. 73, n. 7, p. 608, doi. 10.1071/CH18376
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- Article
Green synthesis of 1,3-dihydrobenzimidazol-2-ones from aromatic diamines by microwave in a tetrabutylammonium bromide-ethanol molten salt paste.
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- Environmental Chemistry Letters, 2018, v. 16, n. 3, p. 1109, doi. 10.1007/s10311-018-0733-8
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- Article
Vitamin B as a metal-free organocatalyst for greener Paal-Knorr pyrrole synthesis.
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- Environmental Chemistry Letters, 2012, v. 10, n. 4, p. 369, doi. 10.1007/s10311-012-0361-7
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- Article
Silica-supported antimony(III) chloride as a mild and reusable catalyst for the Paal-Knorr pyrrole synthesis.
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- Environmental Chemistry Letters, 2012, v. 10, n. 1, p. 5, doi. 10.1007/s10311-011-0321-7
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- Article
Clove bud oil: an efficient, economical and widely available oil for the inhibition of wheat seed germination.
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- Environmental Chemistry Letters, 2011, v. 9, n. 4, p. 519, doi. 10.1007/s10311-011-0312-8
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- Article
ZnCl<sub>2</sub>/Urea Eutectic Solvent as Stable Carbonylation Source for Benign Synthesis of 2–Benzimidazolones and 2–Imidazolones: An Effective Strategy for Preventing NH<sub>3</sub> Gas Evolution.
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- ChemistrySelect, 2019, v. 4, n. 37, p. 11093, doi. 10.1002/slct.201902706
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- Article
Catalytic activity of the nanoporous MCM-41 surface for the Paal–Knorr pyrrole cyclocondensation.
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- Zeitschrift für Naturforschung B: A Journal of Chemical Sciences, 2015, v. 70, n. 7, p. 475, doi. 10.1515/znb-2014-0259
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- Article
Ascorbic acid as a multifunctional hydrogen bonding catalyst for Paal–Knorr synthesis of N-substituted mono- and bis-pyrroles: experimental and theoretical aspects.
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- Research on Chemical Intermediates, 2023, v. 49, n. 9, p. 4087, doi. 10.1007/s11164-023-05072-w
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- Article
Naturally occurring organic acids for organocatalytic synthesis of pyrroles via Paal–Knorr reaction.
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- Research on Chemical Intermediates, 2020, v. 46, n. 12, p. 5255, doi. 10.1007/s11164-020-04260-2
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- Article
Cost-effective fabrication of perdurable electrodeposited TiO<sub>2</sub> nano-layers on stainless steel electrodes applicable to photocatalytic degradation of methylene blue.
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- Research on Chemical Intermediates, 2019, v. 45, n. 9, p. 4275, doi. 10.1007/s11164-017-2899-2
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- Article
Microwave-induced calcium(II) chloride-catalyzed Paal-Knorr pyrrole synthesis: a safe, expeditious, and sustainable protocol.
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- Research on Chemical Intermediates, 2018, v. 44, n. 7, p. 4063, doi. 10.1007/s11164-018-3355-7
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- Article
l-Tryptophan-catalyzed Paal-Knorr pyrrole cyclocondensation: an efficient, clean and recyclable organocatalyst.
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- Research on Chemical Intermediates, 2016, v. 42, n. 2, p. 407, doi. 10.1007/s11164-015-2026-1
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- Article
Crystalline salicylic acid as an efficient catalyst for ultrafast Paal–Knorr pyrrole synthesis under microwave induction.
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- Journal of Chemical Sciences, 2021, v. 133, n. 2, p. 1, doi. 10.1007/s12039-021-01891-9
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- Article
H<sub>2</sub>O<sub>2</sub>-HBr: A metal-free and organic solvent-free reagent system for the synthesis of arylaldehydes from methylarenes.
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- Journal of Chemical Sciences, 2009, v. 121, n. 2, p. 177, doi. 10.1007/s12039-009-0020-0
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- Article
Imidazolium organometallic complex of palladium on Fe<sub>3</sub>O<sub>4</sub> nanoparticles as selective and magnetically recoverable nanocatalyst for C‐C cross‐coupling reactions.
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- Applied Organometallic Chemistry, 2023, v. 37, n. 5, p. 1, doi. 10.1002/aoc.7031
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- Article
Pd(0) complex of fuberidazole modified magnetic nanoparticles: A novel magnetically retrievable high‐performance catalyst for Suzuki and Stille C‐C coupling reactions.
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- Applied Organometallic Chemistry, 2020, v. 34, n. 9, p. 1, doi. 10.1002/aoc.5771
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- Article
Silica-Supported Antimony(III) Chloride as Highly Effective and Reusable Heterogeneous Catalyst for the Synthesis of Quinoxalines.
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- Catalysis Letters, 2009, v. 133, n. 1/2, p. 84, doi. 10.1007/s10562-009-0161-2
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- Article
Enhanced Efficiency of Dye-sensitized Solar Cells Based on Bulk Synthesized TiO<sub>2</sub> Nanorods Annealed at Different Temperatures.
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- Journal of the Chinese Chemical Society, 2015, v. 62, n. 9, p. 811, doi. 10.1002/jccs.201400538
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- Article