Properties and Exciting Facts About 1,5-Diphenylpenta-1,4-dien-3-one

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Nature of the modifying action of white phosphorus on the properties of nanosized hydrogenation catalysts based on bis(dibenzylideneacetone)palladium(0)

The catalytic properties and nature of the nanoparticles forming in the system based on Pd(dba)2 and white phosphorus are reported. A schematic mechanism is suggested for the formation of nanosized palladium-based hydrogenation catalysts. The mechanism includes the formation of palladium nanoclusters via the interaction of Pd(dba)2 with the solvent (N,N-dimethylformamide) and substrate and the formation of palladium phosphide nanoparticles. The inhibiting effect exerted by elemental phosphorus on the catalytic process is due to the conversion of part of the Pd(0) into palladium phosphides, which are inactive in hydrogenation under mild conditions, and the formation of mainly segregated palladium nanoclusters and palladium phosphide nanoparticles. By investigating the interaction between Pd(dba)2 and white phosphorus in benzene, it has been established that the formation of palladium phosphides under mild conditions consists of the following consecutive steps: Pd(0) ? PdP2 ? Pd5P2 ? Pd3P. It is explained why white phosphorus can produce diametrically opposite effects of on the catalytic properties of nanosized palladium-based hydrogenation catalysts, depending on the nature of the palladium precursor.

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Reference£º
Synthesis and Crystal Structure of a Chiral?C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis,
Chiral lanthanide(III) complexes of sulphur¨Cnitrogen¨Coxygen ligand derived from aminothiourea and sodium?D-camphor-¦Â-sulfonate

Some scientific research about 1,5-Diphenylpenta-1,4-dien-3-one

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SYNTHESIS OF SOME 5H-PYRANO- AND 5H-PYRIDO<2',3':4,5>PYRIDO<2,1-b>BENZOTHIAZOL-5-ONE DERIVATIVES

The addition reactions of 3-hydroxy-1H-pyrido<2,1-b>benzothiazol-1-one, 1, have been investigated.Thus, 1 added to aryl isocyanates to give the 2-carbamoyl derivatives 2a,b and to activated alkenes to give the 2-alkylated derivatives 5a-c.Compound 1 reacted also with alpha-substituted cinnamonitriles, 6a-l, to give different products 7, 12, 13 and 15 according to the nature of the substituent in 6.Compounds with the ring systems pyrido<2',3':4,5>pyrido<2,1-b>benzothiazole and pyrano<2',3':4,5>pyrido<2,1-b>benzothiazole have been obtained.The first ring system is a new one.

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Reference£º
Synthesis and Crystal Structure of a Chiral?C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis,
Chiral lanthanide(III) complexes of sulphur¨Cnitrogen¨Coxygen ligand derived from aminothiourea and sodium?D-camphor-¦Â-sulfonate

New explortion of 4254-15-3

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Synthetic Route of 4254-15-3, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.4254-15-3, Name is (S)-Propane-1,2-diol, molecular formula is C3H8O2. In a Article£¬once mentioned of 4254-15-3

ACCURATE DETERMINATION OF THE INTRINSIC RACEMIZATION IN CHIRAL SYNTHESIS VIA ENANTIOMER RESOLUTION OF UNDERIVATIZED VICINAL DIOLS

The accurate assessment of the intrinsic racemization (down to 0.01percent), inherent to reactions typically applied in chiral synthesis, demands for (i) a precursor of almost 100percent e.e. (e.g., S-1a, e.e. >=99.99percent), and (ii) a reliable method for the determination of e.e. of the product (e.g., the derivatization-free enantiomer resolution of the vicinal diol 3a by GC on Chirasil-Val).

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Reference£º
Synthesis and Crystal Structure of a Chiral?C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis,
Chiral lanthanide(III) complexes of sulphur¨Cnitrogen¨Coxygen ligand derived from aminothiourea and sodium?D-camphor-¦Â-sulfonate

Discovery of (S)-Propane-1,2-diol

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Related Products of 4254-15-3, Chemistry is the science of change. But why do chemical reactions take place? Why do chemicals react with each other? The answer is in thermodynamics and kinetics.In a document type is Patent, and a compound is mentioned, 4254-15-3, (S)-Propane-1,2-diol, introducing its new discovery.

CRYSTAL STRUCTURES OF SGLT2 INHIBITORS AND PROCESSES FOR PREPARING SAME

The present invention relates to physical crystal structures of compound of the formula (I): which is an H-1 form, H-2 form or S-PG form, pharmaceutical compositions containing structures of compound I and methods of treating diseases using compound I.

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Reference£º
Synthesis and Crystal Structure of a Chiral?C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis,
Chiral lanthanide(III) complexes of sulphur¨Cnitrogen¨Coxygen ligand derived from aminothiourea and sodium?D-camphor-¦Â-sulfonate

Brief introduction of 4254-15-3

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Stereoselective oxidation of aryl-substituted vicinal diols into chiral alpha-hydroxy aldehydes by re-engineered propanediol oxidoreductase

alpha-Hydroxy aldehydes are chiral building blocks used in synthesis of natural products and synthetic drugs. One route to their production is by regioselective oxidation of vicinal diols and, in this work, we aimed to perform the oxidation of 3-phenyl-1,2-propanediol into the corresponding alpha-hydroxy aldehyde applying enzyme catalysis. Propanediol oxidoreductase from Escherichia coli efficiently catalyzes the stereoselective oxidation of S-1,2-propanediol into S-lactaldehyde. The enzyme, however, shows no detectable activity with aryl-substituted or other bulky alcohols. We conducted ISM-driven directed evolution on FucO and were able to isolate several mutants that were active with S-3-phenyl-1,2-propanediol. The most efficient variant displayed a kcat/KM of 40 s-1 M-1 and the most enantioselective variant an E-value (S/R) of 80. Furthermore, other isolated variants showed up to 4400-fold increased activity with another bulky substrate, phenylacetaldehyde. The results with engineered propanediol oxidoreductases identified amino acids important for substrate selectivity and asymmetric synthesis of aryl-substituted alpha-hydroxy aldehydes. In conclusion, our study demonstrates the feasibility of tailoring the catalytic properties of propanediol oxidoreductase for biocatalytic properties.

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Reference£º
Synthesis and Crystal Structure of a Chiral?C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis,
Chiral lanthanide(III) complexes of sulphur¨Cnitrogen¨Coxygen ligand derived from aminothiourea and sodium?D-camphor-¦Â-sulfonate

The Absolute Best Science Experiment for (S)-Propane-1,2-diol

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Optical resolution, absolute configuration, and activity of the enantiomers of proxyphylline

The enantiomers of proxyphylline have been separated via their corresponding camphanates. Synthesis of (+)-proxyphylline from theophylline and (S)-propylene oxide derived from (S)-lactic acid established the absolute configuration of the (+) and (-) isomer as S and R, respectively. The activity of the enantiomers as cyclic nucleotide phosphodiesterase inhibitors was tested in human lung tissue homogenate. No differences were found either between the two enantiomers or between the enantiomers and racemic proxyphylline.

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Reference£º
Synthesis and Crystal Structure of a Chiral?C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis,
Chiral lanthanide(III) complexes of sulphur¨Cnitrogen¨Coxygen ligand derived from aminothiourea and sodium?D-camphor-¦Â-sulfonate

Extracurricular laboratory:new discovery of 1,5-Diphenylpenta-1,4-dien-3-one

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Synthesis and properties of new tris(cyanoethyl)phosphine complexes of platinum (0,II), palladium (0,II), iridium (I) and rhodium (I). Conformational analysis of tris(cyanoethyl)phosphine ligands

The tris(cyanoethyl)phosphine (tcep) complexes trans-[PtCl2(tcep)2], cis-[PtMe2(tcep)2], and trans-[PtMeCl(tcep)2] are prepared by treatment of the corresponding [PtXY(cod)] (cod = 1,5-cyclooctadiene) with tcep. Reduction of trans-[PtCl2(tcep)2] with NaBH4 gives trans-[PtHCl(tcep)2] which, in the presence of tcep and NEt3, gives the coordinatively unsaturated platinum(0) complex [Pt(tcep)3]. This coordinatively unsaturated species is also formed when [Pt(norbornene)3] reacts with tcep. [Pt(tcep)3] is very unreactive compared to its PEt3 analogue: it is air-stable and does not react with further tcep to form an 18-electron species. It is protonated by HBF4 ¡¤ OEt2 to form [PtH(tcep)3]BF4. The complex trans-[PdCl2(tcep)2] is made from [PdCl2(NCPh)2] and tcep and the derivatives trans-[PdX2(tcep)2] (X = Br or I) are made by metathesis of the dichloro complex. Reduction of trans-[PdCl2(tcep)2] with LiOMe in the presence of tcep gave the palladium(0) complex [Pd(tcep)3] which, like its platinum(0) analogue, undergoes exchange with free tcep on the NMR timescale. The palladium complex reacts with dibenzylideneacetone (dba) to form [Pd(eta2-dba)(tcep)2]; the same product is formed in the reaction of [Pd(eta2-dba)2] and tcep. Reaction of [Pd2Cl2(eta3-C3H3) 2] and tcep gives [PdCl(tcep)(eta3-C3H3)] or [Pd(tcep)2(eta3-C3H3)]Cl depending on stoichiometry. The rhodium(I) and iridium(I) complexes trans-[MCl(CO)(tcep)2], [MCl(tcep)(cod)] and [MCl(tcep)3] are all readily made from tcep and an appropriate precursor. All new compounds have been fully characterised by a combination of elemental analysis, IR, 31P, 13C, 1H and 195Pt NMR spectroscopy. The crystal structure of [IrCl(tcep)3] as a MeCN solvate shows a distorted square planar coordination geometry (trans angles at Ir(I) ca. 164, cis P-Ir-P av. 96, cis P-Ir-Cl av. 85). Analysis of the conformations of tcep ligands in this and other published tcep complexes shows there is a preference for conformations in which aaa, aag or g+g- (a = anti, g = gauche) arrangements of the three M-P-C-C chains are avoided.

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Reference£º
Synthesis and Crystal Structure of a Chiral?C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis,
Chiral lanthanide(III) complexes of sulphur¨Cnitrogen¨Coxygen ligand derived from aminothiourea and sodium?D-camphor-¦Â-sulfonate

Archives for Chemistry Experiments of 24621-61-2

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24621-61-2, Name is (S)-Butane-1,3-diol, belongs to chiral-oxygen-ligands compound, is a common compound. Safety of (S)-Butane-1,3-diolIn an article, once mentioned the new application about 24621-61-2.

Stereoselective beta-C-glycosylation by a palladium-catalyzed decarboxylative allylation: Formal synthesis of aspergillide A

Mild and sweet: The title reaction proceeds under mild conditions with high regio- and diastereoselectivity (see scheme, PG=protecting group, DiPPF=1,1?-bis(diisopropylphosphino)ferrocene). This reaction is suitable for a wide range of glycal-derived gamma-ketone esters and affords C-glycosides with exclusive beta-selectivity. The method was further applied to a concise formal synthesis of aspergillideA. Copyright

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Reference£º
Synthesis and Crystal Structure of a Chiral?C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis,
Chiral lanthanide(III) complexes of sulphur¨Cnitrogen¨Coxygen ligand derived from aminothiourea and sodium?D-camphor-¦Â-sulfonate

Archives for Chemistry Experiments of 1,5-Diphenylpenta-1,4-dien-3-one

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The Stereochemistry of Organometallic Compounds. XXIX Synthesis of Stereoidal 1,4-, 1,3- and 1,6-Diphosphines and Their Evaluation as Ligands in Metal-Catalyzed Asymmetric Synthesis

The steroidal 1,4-diphosphines 3alpha- and 3beta-diphenylphosphino-2alpha-(2′-diphenylphosphinoethyl)-5alpha-cholestanes and their 5H-benzophosphindole derivatives have been prepared and shown to be useful ligands in asymmetric hydrogenation reactions.Interestingly the 3alpha- and 3beta-derivatives lead to opposing enantioselection preferences when used in these reactions.A steroidal 1,3-diphospine, 3alpha-diphenylphosphino-2alpha-diphenylphosphinomethyl-5alpha-cholestane, has been prepared as a mixture containing some of the 3beta-epimer.The 3alpha-1,3-diphosphine led to similar enantioselection in hydrogenation reactions as the 3alpha-1,4-diphosphine, and a model is proposed to explain the sense of the enantioselectivity in the 1,4- and 1,3-diphosphines.A steroidal 1,6-diphosphine has also been prepared but leads to lower optical yields in the hydrogenation reactions.These ligands have been shown to lead to only poor to moderate optical yields when used in asymmetric carbon-carbon bond forming reactions.

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Reference£º
Synthesis and Crystal Structure of a Chiral?C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis,
Chiral lanthanide(III) complexes of sulphur¨Cnitrogen¨Coxygen ligand derived from aminothiourea and sodium?D-camphor-¦Â-sulfonate

Extended knowledge of 1,5-Diphenylpenta-1,4-dien-3-one

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Synthesis, photophysical studies, solvatochromic analysis and TDDFT calculations of diazaspiro compounds

Diazaspiro[5.5]undecane-1,3,5,9-tetraones and 3-thioxo-diazaspiro[5.5]undecane-1,5,9-trione have been synthesized via double Michael addition of 1,5-diphenyl-1,4-pentadien-3-one with active methylene heterocycles N,N-dimethyl barbituric acid, barbituric acid and thiobarbituric acid in water:ethanol (1:1) using TBAB as catalyst. The solvent effect on photophysical behavior of these compounds showed that stokes shift increases with increase in polarity of solvents. The solvent effect on the spectral properties has been investigated by using the Lippert-Mataga and Reichardt methods. The solvatochromism is analyzed by linear solvation energy relationship using the new four-parameter Catalan polarity scales. The relative fluorescence quantum yield of these diazaspiro compounds varies in solvents of different polarity. The HOMO and LUMO energies have been calculated by TDDFT (B3LYP/6-311G (d, p)) approach. TDDFT calculations were also used to compare the experimental and theoretical absorption spectra.

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Reference£º
Synthesis and Crystal Structure of a Chiral?C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis,
Chiral lanthanide(III) complexes of sulphur¨Cnitrogen¨Coxygen ligand derived from aminothiourea and sodium?D-camphor-¦Â-sulfonate