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Cyclic Ru-phenolates were synthesized, and these compounds were used as olefin metathesis catalysts. Investigation of their catalytic activity pointed out that, after activation with chemical agents, these catalysts promote ring-closing metathesis (RCM), enyne and cross-metathesis (CM) reactions, including butenolysis, with good results. Importantly, these latent catalysts are soluble in neat dicyclopentadiene (DCPD) and show good applicability in ring-opening metathesis polymeriyation (ROMP) of this monomer. Olefin metathesis catalysis: Investigation of the catalytic activity of Ru phenolate catalysts pointed out that, after activation with chemical agents, these catalysts promote ring-closing metathesis (RCM), enyne, and cross-metathesis (CM) reactions, including butenolysis, with good results (see scheme, Mes=2,4,6-trimethylphenyl, Cy=cyclohexyl). The phenolanate catalysts, well soluble in dicyclopentadiene (DCPD), also show good applicability in ring-opening metathesis polymerization (ROMP) of this monomer.

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Reference:
Highly efficient and robust molecular ruthenium catalysts for water oxidation,
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

Brief introduction of (1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(phenylmethylene)(tricyclohexylphosphine)ruthenium

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The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.246047-72-3, Name is (1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(phenylmethylene)(tricyclohexylphosphine)ruthenium, molecular formula is C46H65Cl2N2PRu. In a Patent,once mentioned of 246047-72-3, Product Details of 246047-72-3

The present invention relates to relates to macrocyclic small molecule inhibitors of the Sonic Hedgehog signaling pathway, syntheses thereof, and intermediates thereto. Such small molecule modulators of the Sonic Hedgehog signaling pathway are useful in the treatment of proliferative diseases (e.g., basal cell carcinoma, Gorlin syndrome, medulloblastoma, or pancreatic cancer), pulmonary diseases (e.g., interstitial pnuemonitis or interstitial pulmonary fibrosis), and developmental disorders (e.g., phocomelia or cyclopia). Novel non-natural macrocycles are provided that inhibit Sonic Hedgehog induced-protein transcription.

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Reference:
Highly efficient and robust molecular ruthenium catalysts for water oxidation,
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

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A diverse array of multiwalled carbon nanotube (MWCNT) sensory materials have been synthesized and used to create sensors capable of identifying volatile organic compounds (VOCs) on the basis of their functional groups. Functionalized MWCNTs with a series of cross-sensitive recognition groups were successfully synthesized via zwitterionic and post-transformation synthetic procedures. The incorporated chemical functional groups on MWCNT surfaces introduced greatly increased sensitivity and selectivity to the targeted analytes. The distinct response pattern of each chemical was subjected to statistical treatments, which led to a clear separation and accurate identification of 100% of the VOCs. These results demonstrate that covalent functionalized MWCNT-based sensor arrays are a promising approach for low-cost, real time detection and identification of VOCs.

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Reference:
Highly efficient and robust molecular ruthenium catalysts for water oxidation,
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

Final Thoughts on Chemistry for (1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(phenylmethylene)(tricyclohexylphosphine)ruthenium

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A pyrene-tagged ruthenium carbene 8 was synthesized and immobilized on single-walled carbon nanotubes (SWNTs) via pi-pi stacking. These pi-pi interactions were greatly affected by the reaction temperature and the solvent polarity, thus, offering a new reversible immobilization model that can be controlled by reaction temperature in polar solvents, such as acetone. SWNTs-supported ruthenium carbene 8 is a robust and recyclable catalyst system. Six to seven cycles were achieved for ring-closing metathesis of selected substrates. Importantly, after the complete loss of activity, the SWNTs can be easily recycled by washing with tetrahydrofuran. The recycled SWNTs can then be reloaded with 8. The reusability of the catalyst supported on recycled SWNTs is comparable with that supported on fresh SWNTs.

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Reference:
Highly efficient and robust molecular ruthenium catalysts for water oxidation,
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

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The subject matter herein is directed to carbazole-containing sulfonamide derivatives and pharmaceutically acceptable salts or hydrates thereof of structural formula I wherein the variable R1, R2, R3, R4, R5, R6, R7, A, B, C, D, E, F, G, H, a, and b are accordingly described. Also provided are pharmaceutical compositions comprising the compounds of formula I to treat a Cry-mediated disease or disorder, such as diabetes, obesity, metabolic syndrome, Cushing’s syndrome, and glaucoma.

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Reference:
Highly efficient and robust molecular ruthenium catalysts for water oxidation,
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

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The synthesis of the potent antitumor agent (±)-streptonigrin has been achieved in 14 linear steps and 11% overall yield from ethyl glyoxalate. The synthesis features a challenging ring-closing metathesis reaction, followed by elimination and aromatization, to furnish a key pentasubstituted pyridine fragment.

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Reference:
Highly efficient and robust molecular ruthenium catalysts for water oxidation,
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

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A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 246047-72-3, Name is (1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(phenylmethylene)(tricyclohexylphosphine)ruthenium, molecular formula is C46H65Cl2N2PRu. In a Article,once mentioned of 246047-72-3, Computed Properties of C46H65Cl2N2PRu

In order to identify new leads for the treatment of type 2 diabetes, polyenic molecules A and B derived from nipecotic acid and dienol derivatives C have been prepared and their effect on PPARs transcriptional activity evaluated and compared to that of rosiglitazone, WY14,643 and GW501516. Among the synthesized compounds, dienol 39 is the most active, increasing WY14,643 PPARalpha response and demonstrating partial agonist properties on rosiglitazone PPARgamma.

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Reference:
Highly efficient and robust molecular ruthenium catalysts for water oxidation,
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

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Pyrrolizidine, indolizidine, and pyrrolo[1,2-a]azepine substructures are present in a large number of naturally occurring azabicyclic compounds, which are currently of special interest because of their biological activities. To obtain this class of compounds, we envisioned a ring-rearrangement metathesis (RRM) process of 7-azanorbornene systems that incorporates several exocyclic olefin patterns at the nitrogen position. By using this methodology, we have synthesized a set of new 1-azabicyclo[n.3.0]alkenones, which include derivatives of pyrrolam. In all cases, only one regioisomer was obtained. Moreover, new spiro compounds with tricyclic structures have been synthesized by using a domino metathesis process that involves a ring-opening/ring-closing/ring-closing metathesis (ROM/RCM/RCM) sequence. A new synthetic strategy for nitrogen heterocycles was developed that incorporates fused-ring systems and takes advantage of a stereodefined ring-rearrangement metathesis process of substituted 7-azanorbornenes as the stereocontrolled key step. A set of new 1-azabicyclo[n.3.0]alkenones (n = 3, 4, and 5) that include new analogues of pyrrolam were prepared by using this methodology. Copyright

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Reference:
Highly efficient and robust molecular ruthenium catalysts for water oxidation,
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

Brief introduction of (1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(phenylmethylene)(tricyclohexylphosphine)ruthenium

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Disclosed are novel metathesis catalysts of the formula (I), a process for making the same and their use in metathesis reactions such as ring closing or cross metathesis.

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Reference:
Highly efficient and robust molecular ruthenium catalysts for water oxidation,
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

Simple exploration of (1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(phenylmethylene)(tricyclohexylphosphine)ruthenium

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The present invention describes the use of soluble metal salts to reduce impurities and metathesis catalysts poisons from olefinic feedstocks to improve olefin metathesis efficiency. The soluble metal salts were added to the olefinic feedstocks to prevent peroxides and catalyst poisons from inhibiting the metathesis catalyst. The soluble metal salts remain in the olefinic feedstocks and are used without further purification in the olefin metathesis reactions. The key to this invention is the soluble metal salt compounds do not inhibit the olefin metathesis catalysts but unexpectedly increase olefin metathesis catalyst efficiency while prior art heterogeneous metal complexes sequester the olefin metathesis catalyst, preventing olefin metathesis.

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Reference:
Highly efficient and robust molecular ruthenium catalysts for water oxidation,
Catalysts | Special Issue : Ruthenium Catalysts – MDPI