Search results for "Butane"

CCDC 998586: Experimental Crystal Structure Determination

2014

Related Article: Marco De Nardi, Sabrina Antonello, De-en Jiang, Fangfang Pan, Kari Rissanen, Marco Ruzzi, Alfonso Venzo, Alfonso Zoleo, Flavio Maran|2014|ACS Nano|8|8505|doi:10.1021/nn5031143

Selective isomerization of a trans -butanediacetal derivative of tartaric acid with differentiating substituents at C-2 and C-3

2017

Abstract A trans-disubstituted butanediacetal derivative with two different substituents (ester and thioester) – methyl (2R,3R,5R,6R)-3-ethylsulfanylcarbonyl-5,6-dimethoxy-5,6-dimethyl-1,4-dioxane-2-carboxylate, was selectively converted to the cis derivative – methyl (2S,3R,5R,6R)-3-ethylsulfanylcarbonyl-5,6-dimethoxy-5,6-dimethyl-1,4-dioxane-2-carboxylate in high yield on a multigram scale. The product of this reaction offers the possibility for selective modification of one of the substituents, which was demonstrated by Fukuyama reduction of the thioester group.

Asymmetric Synthesis of Fluorinated Monoterpenic Alkaloid Derivatives from Chiral Fluoroalkyl Aldimines via the Pauson‐Khand Reaction

2020

ChemInform Abstract: Gold(I)-Catalyzed Intermolecular Cycloaddition of Allenamides with α,β-Unsaturated Hydrazones: Efficient Access to Highly Substi…

2015

α,β-Unsaturated N,N-dialkyl hydrazones undergo a mild [2 + 2] cycloaddition to allenamides when treated with a suitable gold catalyst. The method, which represents the first application of N,N-dialkyl hydrazones in gold catalysis, is compatible with a wide variety of substituents at the alkenyl moiety of the hydrazone component, proceeds with excellent levels of regio- and diastereoselectivity, and provides densely substituted cyclobutanes with good to excellent yields.

The effect of potassium on the selective oxidation ofn-butane and ethane over Al2O3-supported vanadia catalysts

1995

The catalytic properties of undoped and K-doped (K/V atomic ratio of 0.5) Al2O3-supported vanadia catalysts (∼4.5 wt% of V2O5) for the oxidation ofn-butane and ethane were studied. Isolated tetrahedral V5+ species are mainly observed in both undoped and K-doped samples. The incorporation of potassium decreases both the reducibility of surface vanadium species and the number of surface acid sites. Potassium-free vanadium catalysts show a high selectivity during the oxidative dehydrogenation (ODH) of ethane but a low selectivity during the ODH ofn-butane. However, the presence of potassium on the vanadium catalysts strongly influences their catalytic properties, increasing the selectivity to …

SiO2-supported vanadium magnesium mixed oxides as selective catalysts for the oxydehydrogenation of short chain alkanes

2001

Abstract Unsupported and SiO 2 -supported VMgO mixed oxides catalysts have been prepared, characterized and tested in the oxidation of propane, n -butane and propylene. Mg-vanadates are observed by XRD, IR and Raman spectroscopy in both pure and supported VMgO catalysts, although the effective Mg/V ratio, in the VMgO phases formed, depends on the silica content. Since SiO 2 reacts partially with MgO during the calcination step, forming Mg 2 SiO 4 , the effective Mg/V ratio depends on the silica content. In this sense, pyro -Mg 2 V 2 O 7 is mainly formed on supported catalysts with Mg/V atomic ratios lower than 4, while ortho -Mg 3 V 2 O 8 is observed on supported catalysts with Mg/V atomic …

Gelchromatographie. 1. Mitt. Trennung von oligomeren

1966

Vernetzte Polymere werden hergestellt und ihre Eignung zur gelchromatographischen Trennung von Gemischen von Oligomeren gepruft; im einzelnen wurden untersucht: mit Isocyanaten modifiziertes Sephadex; Polymethyl-und Polybutylmethacrylat, vernetzt mit Glykoldimethacrylat bzw. mit Polyathylenoxid-dimethacrylat; Polyvinylacetat, vernetzt mit n-Butandioldivinylather; Polystrol, vernetzt mit Divinylbenzol; ferner Silicagel. Der Einflus der Molekulgestalt auf das Elutionsvolumen wurde gepruft. Die Elutionsvolumina von p-Oligophenylenen, die eine stabchenformige Molekulgestalt besitzen, sind groser als die von Oligourethanen gleichen Molekulargewichts; o- und m-gewinkelte Oligophenylene zeigen geg…

Cyclodehydration of Diols in Acidic Ionic Liquids

2011

Cyclodehydration of Diols in Acidic Ionic Liquids In the presence of sulfonic acid group functionalized Bronsted-acidic ionic liquids, cyclodehydration of 1,2-ethanediol and 1,4-butanediol is investigated. The role of structure and catalytic activity of ionic liquids on the formation of cyclic ethers: 1,4-dioxane and tetrahydrofuran - is determined.

Mass spectrometric investigation of polymers: Thermal degradation of truxillic and truxinic polyamides

1975

The thermal degradation mechanism of four isomeric truxillic and truxinic polyamides were investigated by direct pyrolysis in the ion source of a mass spectrometer. Thermal degradation reactions were followed directly by this method by detecting the thermal and electron impact-induced fragments. The results obtained have shown that the thermal degradation products are sensibly different for the head-to-head (hh) and head-to-tail (ht) polymers and that the predominant pyrolytic process is the cyclobutane ring cleavage. In the hh isomers, both symmetrical and asymmetrical cyclobutane ring cleavage was detected, while in the ht isomers only symmetrical cleavage occurs; this explains the notice…

Synthesis and photodimerisation of tetrabenzo[ab,f,jk,o][18]annulenes

1999

Abstract The tetrabenzo[ab,f,jk,o][18]annulenes 7a,b, generated in a 5-step synthesis, show photodimerisation and -oligomerisation reactions in the solid state and in solution. The state of aggregation determines the reaction route. Whereas the cyclodimer 8a has a simple cyclobutane structure, the dimer 8b is a highly symmetrical cyclophane.