Search results for "Ether"

WEITERE SELEKTIVITÄTSSTUDIEN AM BEISPIEL EINES ARYLSULFONYLACETYLENS

1984

Abstract With 1-(phenylsulfonyl)propyne-(1) 1 as a model compound, we have investigated the competition reactions with RSH, RNH2 and ROH (R=n-Bu). With RSH and RNH2, the cis-trans-isomeric olefins 2 to 5 are formed. ROH does not react under these conditions. The compounds 6 and 7 are obtained only with ROH as the alcoholate. The reactivity of 1 with nucleophiles is increased in comparison to phenylvinyl sulfone; the selectivity of 1 is, however, decreased. The difference in reactivity of 1 and phenylvinyl sulfone corresponds to ca. 10:1. Mit 1-(Phenylsulfonyl)-propin-(1) 1 als Modellverbindung haben wir die konkurrierenden Umsetzungen mit RSH, RNH2 und ROH (R=n-Bu) studiert. Mit RSH und RNH…

1986

A procedure is described for the preparation of a block copolymer with A-B-A sequences in which ω-ω′-dihydroxy-poly-(ethylene glycol) is inserted between two polymeric monoacidic chains of polycaproamide and bonded to them by means of ester links. The resulting material was characterized. The copolymer is isomorphous with the polycaproamide. Thermal treatments induce a crystalline transition γ α as in polycaproamide. The influence of the moisture content on the glass transition temperature and on the storage modulus is discussed. Ein Verfahren zur Herstellung eines Blockcopolymers mit A-B-A-Sequenzen wird beschrieben. In dem Copolymer ist ω-ω′-Dihydroxy-polyethylenglycol uber Esterbindungen…

Synthese des Methylethers der Herzgift-Methylreduktinsäure ausD-Glucose

1984

Der Methylether 5 der „Herzgift-Methylreduktinsaure” (2), eines Abbauproduktes der Calotropis-Cardenolide, wird in einer mehrstufigen Synthese aus D-Glucose als chiralem Ausgangsmaterial hergestellt. Damit wird die durch Abbaureaktionen getroffene Konfigurationszuordnung fur 2 durch Synthese von 5 bestatigt. Synthesis of the Methyl Ether of “Herzgift-Methylreduktinsaure” Starting from D-Glucose The methyl ether 5 of „Herzgift-Methylreduktinsaure” (2), a degradation product of the Calotropis cardenolides, has been synthesized starting from D-glucose as the chiral pool. The configuration of 2, previously based on the results of degradation, is confirmed by the synthesis of 5.

Kronenethersubstituierte 1,4-Distyrylbenzole und ihre Komplexierung mit Alkalipikraten

2000

Crown Ether Substituted 1,4-Distyrylbenzenes and their Complexation with Alkali Picrates The 1,4-distyrylbenzenes 8 and 9, which contain two crown ether units, each, were prepared by Wittig—Horner reactions. Their complexation tendencies with alkali picrates (Li—Cs) in water/dichloromethane were investigated. Potas sium ions give the strongest complexes. Generally monomo-lecular 1:1-complexes are formed; however, [K-8] + [Pik]—, [K-9]+ [Pik]— and [Rb-8] + [Pik]— generate aggregates, for which a stairway structure is proposed.

(2aRS,3RS,4aSR,6aRS,6bSR)-3-Hydroxy-2a,3,4a,6,6a,6b-hexahydro-1,4-dioxacyclopenta[cd]pentalen-2(5H)-one

2007

The mol­ecular structure of the title compound [enanti­omers (VIII) and (VIIIa)], C8H10O4, was determined in the course of our studies on the synthesis of cyclo­penta­[1,2-b]furan-4-one derivatives. Tricyclic (VIIIa) consists of a planar bridged lactone unit and the two other ring systems in the envelope conformation. It contains five chiral C atoms and was obtained as a racemic mixture. The X-ray analysis showed the compound to possess a half-acetal unit with an endo orientation of the half-acetal ether bridge with respect to the lactone unit.

1984

An apparatus is presented for the precise measurement of vapour pressures. It is tested with diethyl ether and applied to the system tert-butyle acetate/polystyrene (weight-average molecular weight Mw = 110000) up to polymer concentrations of ca. 60 wt.-% in the temperature range from 10 to 90°C; by means of the Redlich-Kister equation the results can well be described analytically. The data are evaluated to yield the Flory-Huggins parameter in the subsequent article in conjunction with other experimental information.

Lithium Ion Recognition with Nanofluidic Diodes through Host-Guest Complexation in Confined Geometries

2018

[EN] The lithium ion recognition is receiving significant attention because of its application in pharmaceuticals, lubricants and, especially, in energy technology. We present a nanofluidic device for specific lithium ion recognition via host guest complexation in a confined environment. A lithium-selective receptor molecule, the aminoethyl-benzo-12-crown-4 (BC12C4-NH2), is designed and functionalized on single conical nanopores in polyethylene terephthalate (PET) membranes. The native carboxylic acid groups on the pore walls are covalently linked with the crown ether moieties and the process is monitored from the changes in the current voltage (I-V) curves. The B12-crown-4 moieties are kno…

Ruthenium(II) meso-tetra-(benzo-15-crown-5)-porphyrinates: synthesis and spectroscopic investigation

2007

The synthesis of novel ruthenium(II) meso-tetra-(benzo-15-crown-5)-porphyrinates, meso-[( B 15 C 5)4 Por ] Ru ( CO )( MeOH ) (1) and meso-[( B 15 C 5)4 Por ] Ru ( L )2 (2)-(4) (meso-[( B 15 C 5)4 Por ]2-= 5,10,15,20-tetrakis-(benzo-15-crown-5)-porphyrinato-dianion; L = pyridine (py), pyrazine (pyz), 4,4′-bipyridyl (4,4′-bpy)), where CO and MeOH , or two N -donor ligands are axially coordinated to the central metal, are reported. The metalation of the free ligand performed by the reaction of Ru 3( CO )12 with meso-[( B 15 C 5)4 Por ] H 2 in 1,2,4-trichlorobenzene (TCB, bp = 215°C), gives (1) in a high yield. The synthesis of (2)-(4) involves the decarbonylation of (1) with trimethylamine N …

Resorcinarene Crowns ☆

2017

Resorcinarene crowns are a class of supramolecular hosts combining a crown ether moiety to a resorcinarene platform as either a podand arm, lower rim substituent, or a bridge. Resorcinarene crowns act as cation hosts and have therefore shown potential in ion transportation and in antibacterial applications.

Proton Acid-induced Rearrangements of α-Alkynylestradiol Methyl Ethers

1993

When subjected to proton catalysis, the α-alkynylestradiol methyl ethers 1a and 1b furnish the Rupe or Meyer-Schuster rearrangement products 2, 4, and 5a. In the presence of sulfuric acid, α-ethynylestradiol 3-methyl ether (1a) is converted into the D-homosteroid 3a. The use of deuterated acids gives rise to the formation of the corresponding deuterated steroids 2b, 2c, 3b, and 5b. Some mechanistic implications of these results are also discussed.