“…Retraction of ‘Transition-metal-free synthesis of conjugated microporous polymers via amine-catalyzed Suzuki–Miyaura coupling reaction’ by Qingmin Liu et al., Chem. …”
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“…Both complexes are effective precatalysts for the Suzuki reaction of aryl chlorides. The reduction of Pd(II) in POPd-Ad and POPd2-Ad by arylboronic acid was examined, and the ideal Pd-to-PA ratio in the Suzuki reaction was found to be 1:1. …”
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“…They were designed and synthesized via a Suzuki–Miyaura cross-coupling reaction using Pd (OH)(2) as a catalyst at a temperature of 65 °C with an intent to obtain improved and safer anti-inflammatory and analgesic agents. …”
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“…Mainly, a great variety of aryl chlorides can be used as substrates for Suzuki–Miyaura and Mizoroki–Heck reactions under mild reaction conditions (60–90 °C) and low catalyst loading (<1 mol% Pd) in aqueous media. …”
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“…A novel thiophene derivative, namely 2,5-diisopropenylthiophene (DIT) was synthetized by Suzuki–Miyaura cross-coupling reaction (SMCCR). The influence of reaction parameters, such as temperature, solvent, stoichiometry of reagents, role of the base and reaction medium were thoroughly discussed in view of yield optimization and environmental impact minimization. …”
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“…We demonstrated the use of these solid catalysts for water-mediated Suzuki–Miyaura coupling reactions. It was found that the surface wettability of the prepared catalysts has an important influence on their catalytic activities. …”
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“…The method was also applied to Suzuki–Miyaura cross-coupling reaction in a one-pot two-step sequential manner, providing a facile and convenient access to the direct synthesis of biaryl compounds from aryl chlorides.…”
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“…2-(3,5-Di-tert-butyl-4-hydroxyphenyl)-5-(4-iodophenyl)-4,4-dimethyl-4H-imidazole 3-oxide reacts with phenylboronic acid and its substituted derivatives in a cross-coupling reaction of the Suzuki–Miyaura type to form 5-biphenyl derivatives of 4H-imidazole-N-oxide. …”
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“…The domino reaction sequence which involves a sequential Suzuki–Miyaura coupling, an intramolecular Diels–Alder reaction, and an aromatization-driven ring-opening isomerization has been shown to give substituted hydroxyfluoranthenes in up to 92% yield. …”
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“…Simple palladium complexes were heterogenized into red algae derived polysaccharide supports, and the effects of polysaccharide, catalyst and solvent types on the performances in a Suzuki cross-coupling reaction were tested. It was found that using palladium salts with sodium triphenylphosphine trisulfonate (TPPTS) as a ligand supported on ι-carrageenans and ethanol as the solvent yielded the best systems. …”
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“…The findings inspire toward a holistic green technology for Suzuki–Miyaura coupling reaction and an innovative avenue for catalyst recycling and product isolation.…”
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“…[Image: see text] Herein we report an investigation into the synthesis, metalation, and functionalization of bis-pocket porphyrins using the Suzuki–Miyaura cross-coupling reaction. Steric limitations to accessing bis-pocket porphyrins were overcome by using this Pd-catalyzed C–C-bond-forming strategy to introduce steric bulk after macrocyclization: 2,6-dibromo-4-trimethylsilybenzaldehyde was condensed with pyrrole, and a variety of boronic acids were coupled to the resulting porphyrin in up to 95% yield. …”
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“…Herein, we describe a marine halogenating enzyme-assisted bioconjugation strategy in which an N-terminal leader peptide guides bromination of a C-terminal Trp residue in genetically encoded peptides and proteins, setting up further Trp arylation by Suzuki–Miyaura reactions. The bromination and subsequent cross-coupling reactions are residue-specific and regiospecific for the indole-6 position, occur under mild aqueous conditions, and do not require any modification of other Trp residues in the substrate peptide and/or protein. …”
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“…When applied as a new catalyst for C–C coupling reactions of Suzuki–Miyaura and Mizoroki–Heck in PEG-400 solvent, the Pd(0)-SMTU-boehmite nanoparticles showed excellent activity and recyclability. …”
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“…In order to prepare diaryl ketone derivatives, we constructed a pallidum (0) complex immobilized on Fe(3)O(4) nanoparticles modified with aminobenzoic acid and phenanthroline [Fe(3)O(4)@ABA/Phen-DCA-Pd(0)], and evaluated its catalytic performance for carbonylative Suzuki-coupling reactions of aryl iodides with aryl boronic acid in the presence of Mo(CO)(6) as the CO source under mild conditions. …”
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“…In contrast to control Tsumura Suzuki Non-obesity (TSNO) mice, TSOD mice were obese and suffered from other metabolic complications. …”
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“…Similarly, dimethyl phenyl[D(1)]methylboronate underwent a Suzuki–Miyaura coupling with bromobenzene to give phenyl[D(1)]methylsilane with 99 % ee. …”
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“…To access new chemical space and build molecular complexity, the Suzuki–Miyaura cross-coupling of brominated 2,1-borazaronaphthalenes has been investigated. …”
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