Search results for "ethanol"

showing 10 items of 2041 documents

Photochemical cyclization of some aldehyde thiosemicarbazones

1992

The photochemical behaviour of some substituted aldehyde thiosemicarbazones 1a-k has been investigated in methanol at 254 nm. Thiosemicarbazones of glyoxil methyl ester 1a-f cyclized to furnish the 3-thioxo- 1,2,4-triazin-5-one 2 ring system. The remaining thiosemicarbazones 1g-j gave 1,2,4-triazoline 4 derivatives.

chemistry.chemical_classificationchemistry.chemical_compoundchemistryOrganic ChemistryMethanolRing (chemistry)PhotochemistryAldehydeSemicarbazoneJournal of Heterocyclic Chemistry
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ChemInform Abstract: Photochemical Cyclization of Some Aldehyde Thiosemicarbazones.

2010

The photochemical behaviour of some substituted aldehyde thiosemicarbazones 1a-k has been investigated in methanol at 254 nm. Thiosemicarbazones of glyoxil methyl ester 1a-f cyclized to furnish the 3-thioxo- 1,2,4-triazin-5-one 2 ring system. The remaining thiosemicarbazones 1g-j gave 1,2,4-triazoline 4 derivatives.

chemistry.chemical_classificationchemistry.chemical_compoundchemistryOrganic chemistryGeneral MedicineMethanolRing (chemistry)PhotochemistryAldehydeChemInform
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A versatile synthesis of 4,5-dihydropyrrolo[1,2-a]quinoxalines

2001

The reaction of 1-(2-aminophenyl)pyrrole with aromatic or heteroaromatic aldehydes in ethanol and catalytic amounts of acetic acid leads to 4,5-dihydropyrrolo[1,2-a]quinoxalines in high yields. When aliphatic aldehydes were used under the same conditions, a slow oxidation to the corresponding pyrrolo[1,2-a]quinoxalines can occur; the oxidation can be avoided by preparing in situ the 5-acetyl derivatives of the 4,5-dihydropyrrolo[1,2-a]quinoxalines.

chemistry.chemical_compoundAcetic acidEthanolChemistryOrganic ChemistryOrganic chemistryCatalysisPyrroleJournal of Heterocyclic Chemistry
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ChemInform Abstract: A Versatile Synthesis of 4,5-Dihydropyrrolo[1,2-a]quinoxalines.

2010

The reaction of 1-(2-aminophenyl)pyrrole with aromatic or heteroaromatic aldehydes in ethanol and catalytic amounts of acetic acid leads to 4,5-dihydropyrrolo[1,2-a]quinoxalines in high yields. When aliphatic aldehydes were used under the same conditions, a slow oxidation to the corresponding pyrrolo[1,2-a]quinoxalines can occur; the oxidation can be avoided by preparing in situ the 5-acetyl derivatives of the 4,5-dihydropyrrolo[1,2-a]quinoxalines.

chemistry.chemical_compoundAcetic acidEthanolchemistryOrganic chemistryGeneral MedicinePyrroleCatalysisChemInform
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Die kolorimetrische bestimmung höhermolekularer phenol-formaldehyd-kondensate in dimethylformamid-methanol-lösung mit FeCl3

1961

Phenol-Formaldehyd-Kondensate geben in einem Gemisch aus Dimethylformamid und Methanol (4:1, Vol.) mit FeCl3 · 6H2O eine Farbreaktion. Es konnten Bedingungen ausfindig gemacht werden, unter denen die Extinktion der Farbreaktion reproduzierbar und innerhalb der Meszeit konstant ist. Diese Farbreaktion wird von konstitutions- und molekulareinheitlichen Phenol-Formaldehyd-Kondensaten bis zum Molekulargewicht 900 gegeben, selbst wenn sie keine Hydroxymethylgruppen besitzen. Bei der Kondensation von 2,6-Dihydroxymethyl-4-methylphenol zu Polyhydroxydibenzylathern (Molekulargewicht bis 3400) zeigt sich eine charakteristische, hypsochrome Verschiebung des Absorptions maximums, wahrend die sauer erh…

chemistry.chemical_compoundAcid catalysischemistryColor reactionPolymer chemistryFormaldehydeDimethylformamideHydroxymethylHypsochromic shiftMethanolMethyleneDie Makromolekulare Chemie
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Der acidolytische abbau von polyoxymethylenen. 18. Mitt. über polyoxymethylene

1962

Beim acidolytischen Abbau von Polyoxymethylendihydraten wurden gaschromatographisch folgende Substanzen identifiziert: Formaldehyd, Wasser, Methanol, Ameisensauremethylester sowie Tri- und Tetraoxymethylen. Die Ausbeute an cyclischen Oligomeren und das Verhaltnis Trioxan/Tetraoxymethylen hangen von der Saure, der Saurekonzentration und der Reaktionszeit ab. Es wird ein Abbaumechanismus vorgeschlagen und diskutiert. In the acidic degradation of polyoxymethylenes the following substances are obtained and identified by gas chromatography: formaldehyde, water, methanol, methyl formate, and also tri- and tetraoxymethylene. The yields of the cyclic oligomers and the ratio trioxane/tetraoxymethyle…

chemistry.chemical_compoundAcid concentrationchemistryTrioxaneMethyl formatePolymer chemistryFormaldehydeMethanolGas chromatographyCatalysisDie Makromolekulare Chemie
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ChemInform Abstract: Hydrophobically Directed Aldol Reactions: Polystyrene-Supported L-Proline as a Recyclable Catalyst for Direct Asymmetric Aldol R…

2008

A simple synthetic methodology for the preparation of a polystyrene-supported L-proline material is reported, and this material has been used as catalyst in direct asymmetric aldol reactions between several ketones and arylaldehydes to furnish aldol products in high yields and stereoselectivities. Screening of solvents showed that these reactions take place only in the presence of water or methanol, at lower levels of conversion in the latter case. This solvent effect, coupled with the observed high stereoselectivities, has been explained in terms of the formation of a hydrophobic core in the inner surface of the resin, whereas the hydrophilic proline moiety lies at the resin/water interfac…

chemistry.chemical_compoundAldol reactionChemistryMoietyOrganic chemistryStereoselectivityGeneral MedicineProlinePolystyreneMethanolSolvent effectsCatalysisChemInform
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Fluoro heterocycles. A photochemical methodology for the synthesis of 3-amino- and 3-(N-alkylamino)-5-perfluoroalkyl-1,2,4-oxadiazoles

2000

Abstract A photochemical methodology for the synthesis of perfluoroalkyl-1,2,4-oxadiazoles has been described. 3-Amino- and 3-( N -alkylamino)-5-perfluoroalkyl-1,2,4-oxadiazoles have been prepared by irradiation of 3-perfluoroalkanoylamino-4-phenyl-1,2,5-oxadiazoles (furazans) at λ =313 nm in methanol and in the presence of ammonia or primary aliphatic amines.

chemistry.chemical_compoundAmmoniaPrimary (chemistry)ChemistryOrganic ChemistryDrug DiscoveryPhotodissociationMethanolIrradiationPhotochemistryBiochemistryTetrahedron Letters
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ChemInform Abstract: Heterocyclic Photorearrangements. Photoinduced Rearrangement of 3-Styryl-1,2,4-oxadiazoles.

1990

The photochemical behaviour of 3-styryl-5-phenyl-(5-methyl)-1,2,4-oxadiazoles in methanol at 254 nm has been investigated. A photoinduced rearrangement to the quinoline system has been pointed out and explained as proceeding through an initial photolysis of the ring ON bond, followed by a six membered ring closure reaction involving the styryl moiety.

chemistry.chemical_compoundChemistryPhotodissociationQuinolineClosure (topology)MoietyGeneral MedicineMethanolRing (chemistry)Medicinal chemistryChemInform
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Ethanol-Based Post-processing of Generator-Derived 68Ga Toward Kit-Type Preparation of 68Ga-Radiopharmaceuticals

2014

Post-processing by means of a cation-exchanger–based protocol is an efficient strategy for purification and concentration of generator-derived 68Ga. It ensures the removal of 68Ge before 68Ga-radiopharmaceutical preparation and high labeling yields of 68Ga-labeled radiopharmaceuticals for routine medical application. Methods: In an effort to overcome the problem associated with acetone in the currently applied method, we have investigated the feasibility of replacing it with ethanol. The purification of 68Ga from coeluted metallic impurities (68Ge4+, Fe3+, Zn2+, and Ti4+) on various cation-exchange columns has been investigated with a variety of post-processing solutions. As a proof of prin…

chemistry.chemical_compoundChromatographyEthanolGenerator (computer programming)ChemistryElutionAcetoneRadiology Nuclear Medicine and imagingFraction (chemistry)Metallic impuritiesJournal of Nuclear Medicine
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