نتایج جستجو برای: inverse phase transfer catalyst

تعداد نتایج: 992446  

2018
Romain Sallio Stéphane Lebrun Frédéric Capet Francine Agbossou-Niedercorn Christophe Michon Eric Deniau

A new asymmetric organocatalyzed intramolecular aza-Michael reaction by means of both a chiral auxiliary and a catalyst for stereocontrol is reported for the synthesis of optically active isoindolinones. A selected cinchoninium salt was used as phase-transfer catalyst in combination with a chiral nucleophile, a Michael acceptor and a base to provide 3-substituted isoindolinones in good yields a...

Journal: :The Journal of organic chemistry 2003
Alessandro Loris Alvise Perosa Maurizio Selva Pietro Tundo

The nucleophilic displacement on n-octylmesylate (n-C(8)H(17)OSO(2)CH(3), 1) with four different anions (I(-), Br(-), N(3)(-), and SCN(-)) is investigated under liquid-supercritical phase-transfer catalysis (LSc-PTC) conditions, i.e. in a biphase system of supercritical carbon dioxide (scCO(2)) and water, in the presence of both silica supported and conventional onium salts. The CO(2) pressure ...

Via the one-pot condensation reaction of ethyl acetoacetate, aromatic aldehydes, 2,4-dinitrophenylhydrazine, and β-naphthol; new pyrazolone derivatives were synthesized in the presence of three Brønsted acid catalysts. These Brønsted acid catalysts are Silica sulfuric acid (SSA), tetra-n-butyl ammonium hydrogen sulfate (TBAHSO4) and [2,2′-Bipyridine]-1,1′-diium tricyanomethanide {[2,2′-BPyH][C(...

Journal: :Journal of computational chemistry 2014
Sateesh Bandaru Niall J. English Andrew D. Phillips J. M. D. MacElroy

Electronic-structure density functional theory calculations have been performed to construct the potential energy surface for H2 release from ammonia-borane, with a novel bifunctional cationic ruthenium catalyst based on the sterically bulky β-diketiminato ligand (Schreiber et al., ACS Catal. 2012, 2, 2505). The focus is on identifying both a suitable substitution pattern for ammonia-borane opt...

ابراهیمی, علیرضا, زنجانچی, محمد علی, طباطبائیان, خلیل, یزدانی, نیلوفر,

The protons on a silica or alu mina su rface can be replaced by manganese( III) porphyrin ca tions, Mn(TPP +). Manganesc(III) porphyrin supported on silica and alumina can activate dioxygen in the presence of additional NaBH4 o r [NBu41rBH41 as an electron source and styrene, affording I-phenyl ethanol and acetophenone in a 4:1 ratio. When oxidation was applied in a mixture of benzene/eth...

Journal: :Organic & biomolecular chemistry 2011
Li-Qian Cui Kai Liu Chi Zhang

Catalytic oxidation of benzylic C-H bonds could be efficiently realized using IBS as a catalyst which was generated in situ from the oxidation of sodium 2-iodobenzenesulfonate (1b) by Oxone in the presence of a phase-transfer catalyst, tetra-n-butylammonium hydrogen sulfate, in anhydrous acetonitrile at 60 °C. Various alkylbenzenes, including toluenes and ethylbenzenes, several oxygen-containin...

A general, mild and efficient protocol has been developed for the synthesis of esters and thioesters. The process has been taking place using tetra n-butylammonium iodide (TBAI) as a phase-transfer catalyst and in the presence of potassium carbonate (K2CO3). A wide range of esters and thioesters was prepared in high yields and suitable times by the treatment of alcohols, phenols and thiols with...

1997
Bernard Widrow Gregory L. Plett

An unknown linear plant will track an input command signal if the plant is driven by a controller whose transfer function approximates the inverse of the plant transfer function. An adaptive inverse identification process can be used to obtain a stable controller, even if the plant is nonminimum phase. A model-reference version of this idea allows system dynamics to closely approximate desired ...

Bahman Vasheghani Farahani Farzaneh Hossein Poor Rajabi, Mir Mohammad Alavi Nikje Narges Sabouri

Cis-polybutadiene was functionalized using in–situ generated DMD as oxidant and tetra-n-butyl ammonium bromide as phase transfer catalyst (PTC). The epoxidation process was investigated by 1HNMR spectroscopy. 1HNMR spectrum analysis of products confirms the absence of ring opening side products in epoxidation reaction. Various factors such as reaction temperature, reaction time and the concentr...

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