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Epoxy compounds usually have stronger nucleophilic ability, because the alkyl group on the oxygen atom makes the bond angle smaller, which makes the lone pair of electrons react more dissimilarly with the electron-deficient system. Compound: Ruthenium(III) chloride xhydrate, is researched, Molecular Cl3H2ORu, CAS is 14898-67-0, about Constructing amorphous RuxOy on CuO/Cu2O nanowire arrays for improved oxygen evolution.Application of 14898-67-0.

Developing a facile strategy for the construction of advanced electrocatalysts to accelerate oxygen evolution kinetics to meet the needs of new energy conversion technologies is highly desirable. Herein, a novel and facile route is devised to grow the amorphous RuxOy on CuO/Cu2O nanowire arrays. Exptl. results show that the typical product displays an outstanding electrocatalytic oxygen evolution activity involving a low overpotential of 236 mV at 20 mA cm-2 and an excellent durability. The reasons for which is associated with the synergistic effect of amorphous RuxOy on CuO/Cu2O nanowire arrays, as well as the existence of abundant oxygen vacancies. This study exhibits new insights into using the composite of amorphous RuxOy and copper (Cu)-based oxides as high-activity catalysts for oxygen evolution.

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Reference:
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

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The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: [Ir(dtbbpy)(ppy)2]PF6( cas:676525-77-2 ) is researched.Product Details of 676525-77-2.Tlahuext-Aca, Adrian; Garza-Sanchez, R. Aleyda; Glorius, Frank published the article 《Multicomponent Oxyalkylation of Styrenes Enabled by Hydrogen-Bond-Assisted Photoinduced Electron Transfer》 about this compound( cas:676525-77-2 ) in Angewandte Chemie, International Edition. Keywords: multicomponent oxyalkylation styrene hydrogen bond assisted photoinduced electron transfer; acyloxy phthalimide iridium catalyzed condensation styrene photoinduced electron transfer; alkyl radicals; decarboxylation; hydrogen bonding; oxyalkylation; photoredox catalysis. Let’s learn more about this compound (cas:676525-77-2).

Herein, authors disclose a strategy for the activation of N-(acyloxy)phthalimides towards photoinduced electron transfer through hydrogen bonding. This activation mode enables efficient access to C(sp3)-centered radicals upon decarboxylation from bench-stable and readily available substrates. Moreover, they demonstrate that the formed alkyl radicals can be successfully employed in a novel redox-neutral method for constructing sp3-sp3 bonds across styrene moieties that gives straightforward access to complex alc. and ether scaffolds.

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Reference:
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

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The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: (S)-3-((S)-2-(((S)-1-Ethoxy-1-oxo-4-phenylbutan-2-yl)amino)propanoyl)-1-methyl-2-oxoimidazolidine-4-carboxylic acid hydrochloride( cas:89396-94-1 ) is researched.Recommanded Product: (S)-3-((S)-2-(((S)-1-Ethoxy-1-oxo-4-phenylbutan-2-yl)amino)propanoyl)-1-methyl-2-oxoimidazolidine-4-carboxylic acid hydrochloride.Saruta, Takao; Omae, Teruo; Kuramochi, Morio; Iimura, Osamu; Yoshinaga, Kaoru; Abe, Keishi; Ishii, Masao; Watanabe, Tsutomu; Takeda, Tadanao published the article 《Imidapril hydrochloride in essential hypertension: A double-blind comparative study using enalapril maleate as a control》 about this compound( cas:89396-94-1 ) in Journal of Hypertension. Keywords: imidapril hydrochloride enalapril maleate antihypertensive. Let’s learn more about this compound (cas:89396-94-1).

The objective was to assess the value of using imidapril hydrochloride (ACE/TA-6366), a long-acting angiotensin converting enzyme (ACE) inhibitor developed in Japan, to treat patients with essential hypertension. A double-blind, comparative, phase III study was carried out using enalapril maleate as a control, with a 4-wk observation period and a 12-wk treatment period. Both drugs were started at a dose of 5 mg once a day, increasing to 10 mg in patients whose antihypertensive response was insufficient after 4 wk. The study included 231 outpatients aged 30-74 yr; of these, 108 in the imidapril group and 115 in the enalapril group were assessed. There were no differences in background factors between groups. An adequate antihypertensive effect was observed in 71.3% (77/108) in the imidapril group and in 66.1% (76/115) in the enalapril group, with no significant difference between groups. The pulse rate was unchanged in both groups. The drug had no adverse effects in 86.1% (93/108) of the imidapril group and 79.1% (91/115) of the enalapril group, with no significant difference between groups. Adverse drug effects were observed in 5.6% (6/108) of the imidapril group and 12.2% (14/115) of the enalapril group. Cough was the most frequent side effect, reported in 0.9% (1/108) of the imidapril group and 7.0% (8/115) of the enalapril group. Other side effects were reported in 4.6% (5/108) of the imidapril group and 5.2% (6/115) of the enalapril group. Abnormal laboratory values were observed in 3.7% (4/108) of the imidapril group and 0.9% (1/115) of the enalapril group. Imidapril showed excellent clin. efficacy and safety compared to enalapril. The low incidence of cough is of particular interest.

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Reference:
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

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The three-dimensional configuration of the ester heterocycle is basically the same as that of the carbocycle. Compound: 4-Hydroxyquinoline-2-carboxylic Acid(SMILESS: O=C(C1=NC2=CC=CC=C2C(O)=C1)O,cas:492-27-3) is researched.Synthetic Route of C9H8N2. The article 《Kynurenine pathway metabolites in cerebrospinal fluid and blood as potential biomarkers in Huntingtons disease》 in relation to this compound, is published in Journal of Neurochemistry. Let’s take a look at the latest research on this compound (cas:492-27-3).

Converging lines of evidence from several models, and post-mortem human brain tissue studies, support the involvement of the kynurenine pathway (KP) in Huntingtons disease (HD) pathogenesis. Quantifying KP metabolites in HD biofluids is desirable, both to study pathobiol. and as a potential source of biomarkers to quantify pathway dysfunction and evaluate the biochem. impact of therapeutic interventions targeting its components. In a prospective single-site controlled cohort study with standardised collection of cerebrospinal fluid (CSF), blood, phenotypic and imaging data, we used high-performance liquid-chromatog. to measure the levels of KP metabolites-tryptophan, kynurenine, kynurenic acid, 3-hydroxykynurenine, anthranilic acid and quinolinic acid-in CSF and plasma of 80 participants (20 healthy controls, 20 premanifest HD and 40 manifest HD). We investigated short-term stability, intergroup differences, associations with clin. and imaging measures and derived sample-size calculation for future studies. Overall, KP metabolites in CSF and plasma were stable over 6 wk, displayed no significant group differences and were not associated with clin. or imaging measures. We conclude that the studied metabolites are readily and reliably quantifiable in both biofluids in controls and HD gene expansion carriers. However, we found little evidence to support a substantial derangement of the KP in HD, at least to the extent that it is reflected by the levels of the metabolites in patient-derived biofluids.

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Reference:
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

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Formula: C27H18AlN3O3. Aromatic compounds can be divided into two categories: single heterocycles and fused heterocycles. Compound: Aluminum triquinolin-8-olate, is researched, Molecular C27H18AlN3O3, CAS is 2085-33-8, about Highly transparent, low sheet resistance and stable Tannic acid modified-SWCNT/AgNW double-layer conductive network for organic light emitting diodes. Author is Zhu, Ze-Ru; Geng, Wenming; Zhu, Qingxia; Ethiraj, Anita Sagadevan; Wang, Tao; Jing, Li-Chao; Ning, Yu-Jie; Tian, Yi; Geng, Wen-Hao; Wu, Lei; Geng, Hong-Zhang.

In this paper, we used tannic acid (TA) functionalized carbon nanotubes (TCNTs), and silver nanowires (AgNWs) to construct a new type of transparent conductive film (TCF) with a double-layered conductive network structure. The hybrid film exhibits excellent light transmittance, high elec. conductivity, ultra-flexibility, and strong adhesion. These outstanding performances benefit from the filling and adhesion of hydrophilic TCNT layers to the AgNW networks. Besides, we introduced the post-treatment process of mech. pressing and covering polymer conductive polymer PEDOT:PSS, which obtained three layers of TCNT/AgNW/PEDOT hybrid film and greatly improved the comprehensive properties. The hybrid film can reach a sheet resistance of 9.2 ω sq-1 with a transmittance of 83.4% at 550 nm wavelength, and a low root mean square (RMS) roughness (approx. 3.8 nm). After 10 000 bends and tape testing, the conductivity and transmittance of the hybrid film remain stable. The resistance of the film has no significant degradation after 14 d of exposure to high temperature of 85°C and humidity of 85%, indicating excellent stability. The organic light-emitting diodes (OLEDs) with TCNT/AgNW/PEDOT hybrid film as anode exhibit high c.d. and luminosity, confirming this process has considerable potential application in photovoltaic devices.

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Reference:
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

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HPLC of Formula: 676525-77-2. The protonation of heteroatoms in aromatic heterocycles can be divided into two categories: lone pairs of electrons are in the aromatic ring conjugated system; and lone pairs of electrons do not participate. Compound: [Ir(dtbbpy)(ppy)2]PF6, is researched, Molecular C40H40F6IrN4P, CAS is 676525-77-2, about A Radical Cascade Enabling Collective Syntheses of Natural Products. Author is Wang, Xiaobei; Xia, Dongliang; Qin, Wenfang; Zhou, Ruijie; Zhou, Xiaohan; Zhou, Qilong; Liu, Wentao; Dai, Xiang; Wang, Huijing; Wang, Shuqing; Tan, Ling; Zhang, Dan; Song, Hao; Liu, Xiao-Yu; Qin, Yong.

An efficient photocatalytic radical cascade method that enabled access to libraries of chiral and multiple-ring-fused tetrahydrocarbolinones such as I [R = Me, CH2CN, Bn, etc.], II [R1 = (CH2)2CN, (CH2)2Ac, CH=CHAc, etc.] and III [R2 = CHO, Ac, CN, etc.; R3 = H, OMe; EWG = Ac, CO2Me, C(O)CH2OTBS] was reported. The radical cascade could controllably introduced complexity and functionality into products with excellent chemo-, regio- and diastereoselectivity. The power of this distinct method was demonstrated by the efficient synthesis of 33 monoterpenoid indole alkaloids belonging to four families. Promisingly, the radical cascade was green, water insensitive and readily scalable.

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Reference:
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

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Fields, Ashley M.; Welle, Kevin; Ho, Elaine S.; Mesaros, Clementina; Susiarjo, Martha published the article 《Vitamin B6 deficiency disrupts serotonin signaling in pancreatic islets and induces gestational diabetes in mice》. Keywords: vitamin B6 deficiency gestational diabetes serotonin pancreatic islets signaling.They researched the compound: 4-Hydroxyquinoline-2-carboxylic Acid( cas:492-27-3 ).Category: copper-catalyst. Aromatic heterocyclic compounds can be divided into two categories: single heterocyclic and fused heterocyclic. In addition, there is a lot of other information about this compound (cas:492-27-3) here.

In pancreatic islets, catabolism of tryptophan into serotonin and serotonin receptor 2B (HTR2B) activation is crucial for β-cell proliferation and maternal glucose regulation during pregnancy. Factors that reduce serotonin synthesis and perturb HTR2B signaling are associated with decreased β-cell number, impaired insulin secretion, and gestational glucose intolerance in mice. Albeit the tryptophan-serotonin pathway is dependent on vitamin B6 bioavailability, how vitamin B6 deficiency impacts β-cell proliferation during pregnancy has not been investigated. In this study, we created a vitamin B6 deficient mouse model and investigated how gestational deficiency influences maternal glucose tolerance. Our studies show that gestational vitamin B6 deficiency decreases serotonin levels in maternal pancreatic islets and reduces β-cell proliferation in an HTR2B-dependent manner. These changes were associated with glucose intolerance and insulin resistance, however insulin secretion remained intact. Our findings suggest that vitamin B6 deficiency-induced gestational glucose intolerance involves addnl. mechanisms that are complex and insulin independent.

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Reference:
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

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Name: (S)-3-((S)-2-(((S)-1-Ethoxy-1-oxo-4-phenylbutan-2-yl)amino)propanoyl)-1-methyl-2-oxoimidazolidine-4-carboxylic acid hydrochloride. Aromatic heterocyclic compounds can also be classified according to the number of heteroatoms contained in the heterocycle: single heteroatom, two heteroatoms, three heteroatoms and four heteroatoms. Compound: (S)-3-((S)-2-(((S)-1-Ethoxy-1-oxo-4-phenylbutan-2-yl)amino)propanoyl)-1-methyl-2-oxoimidazolidine-4-carboxylic acid hydrochloride, is researched, Molecular C20H28ClN3O6, CAS is 89396-94-1, about Imidapril: a review of its use in essential hypertension, type 1 diabetic nephropathy and chronic heart failure. Author is Robinson, Dean M.; Curran, Monique P.; Lyseng-Williamson, Katherine A..

A review. Imidapril (Tanatril), through its active metabolite imidaprilat, acts as an ACE inhibitor to suppress the conversion of angiotensin I to angiotensin II and thereby reduce total peripheral resistance and systemic blood pressure (BP). In clin. trials, oral imidapril was an effective antihypertensive agent in the treatment of mild to moderate essential hypertension. Some evidence suggests that imidapril also improves exercise capacity in patients with chronic heart failure (CHF) and reduces urinary albumin excretion rate in patients with type 1 diabetes mellitus. Imidapril was well tolerated, with a lower incidence of dry cough than enalapril or benazepril, and is a first choice ACE inhibitor for the treatment of mild to moderate essential hypertension. Pharmacol. Properties The active metabolite of imidapril is imidaprilat, which inhibits the conversion of angiotensin I to angiotensin II. Lowering of plasma and tissue angiotensin II levels results in peripheral vasodilation, reduced systemic BP, renoprotective effects in patients with type 1 diabetes, and decreased renal sodium and water retention. After multidose oral administration in patients with hypertension, steady-state maximum plasma concentrations of imidapril (≈30 ng/mL) and imidaprilat (≈20 ng/mL) are achieved in a median time of 2 and 5 h. In healthy men 25.5% of a single dose of imidapril 10mg was excreted in the urine within 24 h. Elimination occurs primarily through excretion in the urine (≈40%) and feces (≈50%); after oral administration in healthy volunteers, the terminal elimination half-life of imidaprilat is ≈24 h. Therapeutic Efficacy In randomized controlled trials, oral imidapril was effective in the treatment of adults with mild to moderate essential hypertension. In short-term (2- and 4-wk) dose-finding trials, imidapril dosages of 10-40 mg/day were significantly more effective than placebo, inducing 11-15mm Hg reductions in sitting diastolic BP (sDBP; primary endpoint). In comparative 12- and 24-wk trials, imidapril 5-20 mg/day induced reductions in mean sDBP of 10-15mm Hg that did not differ significantly from those induced by hydrochlorothiazide 12.5-50 mg/day or captopril 50-100 mg/day (primary endpoint), nor those induced by enalapril 5-10 mg/day or nifedipine sustained release (SR) 40-80 mg/day (secondary endpoint). In addition, reductions in sDBP and sitting systolic BP (co-primary endpoints) with imidapril did not differ from those induced by candesartan 4-16 mg/day. Favorable reductions in sDBP were maintained during 6-mo and 52-wk noncomparative trials. In patients with type 1 diabetes, the urinary albumin excretion rate (a marker of nephropathy) increased by 72% in placebo recipients, but declined by 41% in imidapril 5 mg/day and by 6% in captopril 37.5 mg/day recipients during a mean treatment period of 1.5 years. In patients with CHF, mean total exercise time increased from baseline in imidapril 2.5-10 mg/day recipients in a dose-related manner after 12-wk of treatment; a 9.7% increase with imidapril 10 mg/day was significantly greater than the change with placebo (+0.7%). Tolerability Overall, imidapril was relatively well tolerated, with an incidence of adverse events in pooled analyses of data from clin. trials and post-marketing surveillance (n = 6632) of 6.6%. The most commonly reported adverse events were cough, hypotension, dizziness and pharyngeal discomfort. During 2- and 4-wk trials, the overall incidence of adverse events was 26% and 40% in recipients of imidapril 2.5-40 mg/day compared with 35% and 37% in placebo recipients. In comparative trials, the incidence of treatment-related adverse events in imidapril vs. enalapril recipients in two 12-wk trials were 5.6% vs. 12.2% and 12.0% vs. 14.1%; in other 12-wk trials treatment-related adverse events were observed in 24.2% of imidapril vs. 41.7% of nifedipine SR, and 20.7% of imidapril vs. 46.4% of captopril recipients, while the overall incidence of adverse events in imidapril vs. candesartan recipients was 11.7% vs. 16.1%. The incidences of adverse events in a 24-wk trial were 46.0% with imidapril and 52.8% with hydrochlorothiazide. In longer-term trials, adverse events were reported by 61.6% of imidapril recipients in the 52-wk trial; however, only 1.7% of imidapril recipients in a 6-mo field trial experienced adverse events considered related to ACE inhibitor treatment. In prospective investigations in hypertensive patients, switching to imidapril did not reduce the incidence of cough (a class effect of ACE inhibitors) in a small open-label trial in hypertensive patients already experiencing ACE-inhibitor induced cough; however, in a large crossover trial, the incidence of cough with imidapril (15.2%) was less than half that with enalapril (38.6%). In addition, cough disappeared in 52.9% of enalapril recipients switched to imidapril, and in patients without cough during imidapril treatment, switching to enalapril induced cough in 20.9%. In contrast, in patients without cough during initial enalapril treatment, only 0.9% developed cough during subsequent imidapril treatment. In a second large, double-blind crossover trial, the incidence of cough was significantly lower in imidapril than benazepril recipients.

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Reference:
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

Extracurricular laboratory: Synthetic route of 20859-23-8

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Related Products of 20859-23-8. The mechanism of aromatic electrophilic substitution of aromatic heterocycles is consistent with that of benzene. Compound: (S)-2-Bromosuccinic acid, is researched, Molecular C4H5BrO4, CAS is 20859-23-8, about Stereoselective total synthesis of obolactones and 7′,8′-dihydroobolactones. Author is Saini, Deepak; Kumar, Praveen; Fernandes, Rodney A..

A concise stereoselective total synthesis of two diastereomeric obolactones and 7′,8′-dihydroobolactones has been achieved using a metal-free catalytic δ-hydroxyalkynone rearrangement, which could provide the required dihydro-γ-pyrone moiety. The desired first stereogenic center was installed through the chiral pool material, L-aspartic acid. Next, the allylation reaction was strategically utilized to provide the requisite olefin bond for the intended ring-closing metathesis, allowing the installation of the remaining dihydro-α-pyrone moiety in the natural products. It also enabled the targeting of both dihydro-α-pyrone diastereomers. Thus, the first stereoselective total synthesis of (+)-7′,8′-dihydroobolactone was accomplished, establishing its structure and absolute configuration.

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Reference:
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

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Reference of [Ir(dtbbpy)(ppy)2]PF6. Aromatic compounds can be divided into two categories: single heterocycles and fused heterocycles. Compound: [Ir(dtbbpy)(ppy)2]PF6, is researched, Molecular C40H40F6IrN4P, CAS is 676525-77-2, about Engineering Charge Injection Interfaces in Hybrid Light-Emitting Electrochemical Cells. Author is Roldan-Carmona, Cristina; Akatsuka, Takeo; Sessolo, Michele; Watkins, Scott E.; Bolink, Henk J..

Light-emitting electrochem. cells (LECs) consists of a thin film of an ionic organic semiconductor sandwiched between two electrodes. Because of the large d. of ions, LECs are often reported to perform independently on the electrodes work function. Here the authors use metal oxides as charge injection layers and demonstrate that, although electroluminescence is observed independently of the electrodes used, the device performances are strongly dependent on the choice of the interface materials. Relying on metal oxide charge injection layers, such hybrid devices are of interest for real lighting applications and could pave the way for new efficient, stable, low-cost lighting sources.

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Reference:
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”