Search results for "Aliphatic compound"

showing 10 items of 53 documents

Fluoreszierende silane als OH-selektive schutzgruppen

1985

Abstract Fluorescent tertiary silanes are synthesized which, under cesium fluoride/ imidazole activation, discriminate between primary and secondary OH groups. Serine n-butylamide reacts with [5-dimethylamino(1-naphthyl)]dimethylsilane ( 1 ) and diisopropyl[5-dimethylamino(1-naphthyl)]silane ( 2 ) to form the silyl ethers (−)- l -3-[5-dimethylamino(1-naphthyl)]-dimethylsilyloxy]serine n-butylamid ( 14 ) and (−)- l -3-[diisopropyl[5-dimethylamino(1-naphthyl)]silyloxy]serine n-butylamid ( 15 ) exclusively. The silyl ethers are cleaved on treatment with H 2 F 2 , forming the corresponding fluorescent silyl fluorides. Absorption and fluorescence data as well as stability data for the hydrolysis…

SilanesDimethylsilaneSilylationChemistrymedicine.drug_classStereochemistryOrganic ChemistryCarboxamideBiochemistryMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundpolycyclic compoundsMaterials ChemistrymedicineImidazolePhysical and Theoretical ChemistryProtecting groupAliphatic compoundFluorideJournal of Organometallic Chemistry
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Gas chromatography of homologous esters

1984

Abstract The gas chromatographic retention behaviour of the propanoyl and monochloropropanoyl esters of saturated C3C5 branched-chain and unsaturated C3C6 alcohols on SE-30 and OV-351 capillary columns at several temperatures is reported. Retention index increments at 80 and 120°C show the effect of branching in the alkyl chain and also the effect of unsaturation and of its position in the chain with chlorination at the two possible positions in the acyl chain. The various incremental effects are discussed and compared with the behaviour of the corresponding n-alkyl esters.

Steric effectsCapillary actionCarboxylic acidchemistry.chemical_elementBranching (polymer chemistry)BiochemistryAnalytical ChemistryHomologous serieschemistry.chemical_compoundCapillary columnpolycyclic compoundsChlorineOrganic chemistryChlorine substituentAlkylchemistry.chemical_classificationDegree of unsaturationChromatographyOrganic ChemistryChloroacetatesGeneral MedicinechemistryAcyl chainKovats retention indexNon polarGas chromatographyAliphatic compoundJournal of Chromatography A
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Durch sterische effekte stabilisierte ß-ketocarbonsäuren

1989

Abstract Increasing steric hindrance in β-keto carboxylic acids leads to an increasing kinetic stability towards decarboxylation, till systems are reached which are completely stable at room temperature. Simultaneously the tautomeric equilibrium is changed in favour of the (Z)-enol, and finally in favour of the (E)-configurated enol.

Steric effectschemistry.chemical_compoundChemistryDecarboxylationOrganic ChemistryDrug DiscoveryOrganic chemistryKeto–enol tautomerismAliphatic compoundBiochemistryMedicinal chemistryTautomerEnolTetrahedron Letters
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Unsaturated carboxylic acid dienolates. Addition to substituted cyclohexanones. Inverted kinetic and thermodynamic stereoselectivities.

1987

Abstract Addition of the lithium dienolate derived from crotonic acid to monosubstituted cyclohexanones occurs through the α and γ carbon atoms of the dienolate in the cold and on heating, respectively. For any regioselectivity, equatorial approach is found under kinetic conditions, but equilibration favours products from axial attack and selectivity may be inverted.

chemistry.chemical_classificationAddition reactionKetoneCarboxylic acidOrganic Chemistrychemistry.chemical_elementRegioselectivityBiochemistryMedicinal chemistrychemistryDrug DiscoveryOrganic chemistryLithiumStereoselectivityAliphatic compoundSelectivityTetrahedron Letters
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Trienediolates of hexadienoic acids in synthesis. synthesis of retinoic and nor-retinoic acids.

1993

Abstract Double deprotonation of either (E,E)-3-methyl-2,4-hexadienoic acid 2, or 4,6-dimethyldihydro-2-pyrone 3 generates apparently the same lithium trienediolate, which affords ω-hydroxy acids 9 on reaction with ketones 7. Hydroxy acids 9 are easily dehydrated to octatrienoic acids 5, which are structurally related to retinoic acid. Similarly, sorbic acid 1 leads to nor-retinoic acid analogs 6.

chemistry.chemical_classificationAddition reactionKetoneChemistryOrganic ChemistryRetinoic acidBiochemistrychemistry.chemical_compoundDeprotonationDrug DiscoveryOrganic chemistryStereoselectivityAliphatic compoundSorbic acidAcetophenoneTetrahedron
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Dienediolates of unsaturated carboxylic acids in synthesis. Synthesis of cyclohexenones and polycyclic ketones by tandem Michael-Dieckmann decarboxyl…

1994

Abstract Substituted 2-cyclohexenones 4 to 7 and hexaxydronaphthalenones and hexahydroindenones 13 to 18 are prepared by tandem Michael-Dieckmann addition of lithium dienediolates of acyclic and alicyclic unsaturated carboxylic acids to the lithium salts of the same or other unsaturated carboxylic acids.

chemistry.chemical_classificationAnnulationCarboxylic acidOrganic ChemistryBiochemistryCinnamic acidchemistry.chemical_compoundAlicyclic compoundchemistryCascade reactionDrug DiscoveryMichael reactionOrganic chemistryAliphatic compoundEnoneTetrahedron
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Reductive transformations - 11. stereoselective cycloannelation and bridging of the cyclooctatetraene dianionMakromol. Chem., Rapid. Commun. 1988, 9,…

1988

Abstract Bifunctional electrophiles with C4-, C6-, and C8-chains are reacted with the cyclooctatetraene dianion to selectively give novel cycloannelation and bridging products which possess a surprising stereochemistry and are useful starting compounds for further syntheses.

chemistry.chemical_classificationAnnulationStereochemistryOrganic ChemistryHalocarbonBiochemistrychemistry.chemical_compoundCyclooctatetraenePolycyclic compoundchemistryDrug DiscoveryElectrophileStereoselectivityBifunctionalAliphatic compoundTetrahedron Letters
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Elektrocarboxylierung organischer Chloride mit Zehrandon

1984

Carboxylation par CO 2 de chloro-1 propane, -butane, α-chlorotoluene, dichlorobenzene, chloro-1 naphtalene et chloro-1p ethylbenzene en presence d'une anode de Al dans DMF-bromure de tetrabutylammonium

chemistry.chemical_classificationBicyclic moleculeCarboxylic acidchemistry.chemical_elementGeneral MedicineElectrochemistryButyric acidchemistry.chemical_compoundchemistryCarboxylationAluminiumCarboxylateAliphatic compoundNuclear chemistryAngewandte Chemie
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Quantitative determination of the main aliphatic carboxylic acids in wood kraft black liquors by high-performance liquid chromatography-mass spectrom…

2006

The versatile characterization of organic material and especially of the significant aliphatic hydroxy acids in black liquor is of great importance, for example, in monitoring the progress of the kraft pulping process. This paper describes a simple high-performance liquid chromatographic separation method with atmospheric-pressure chemical ionization mass spectrometry (HPLC-APCI-MS) which was developed for the rapid quantitative analysis of these acids, mainly formed as the alkaline degradation products of feedstock carbohydrates. The fraction of carbohydrate degradation products is mainly composed of hydroxy monocarboxylic and volatile acids (formic and acetic acids) along with lesser amou…

chemistry.chemical_classificationChemical ionizationChromatographyChemistryCarboxylic acidOrganic ChemistryCarboxylic AcidsGeneral MedicineBiochemistryLigninWoodMass SpectrometryAnalytical ChemistryDicarboxylic acidKraft processLiquid chromatography–mass spectrometryOrganic chemistryAliphatic compoundKraft paperBlack liquorChromatography High Pressure LiquidJournal of chromatography. A
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Large Scale Synthesis of Mono- and Di-urethane Derivatives of Lysine.

1999

Orthogonally protected diurethane derivatives of lysine are valuable materials for peptide syntheses. An example is ZLys(Boc), which is exploited in the industrial production of certain well-established peptide drugs. 3,4) Another derivative is Fmoc-Lys(Boc), which is in common use in the laboratory synthesis of peptides. 5) The simplest route to these lysine derivatives seems to be using the copper complex for simultaneous protection of the a-amino and a-carboxyl function, N e -tert-butoxycarbonylation and then copper detachment. The obtained Lys(Boc) might be then subjected to N a -benzyloxycarbonylation.

chemistry.chemical_classificationCopper complexStereochemistryLysinechemistry.chemical_elementPeptideGeneral ChemistryGeneral MedicineCopperChemical synthesisDerivative (finance)chemistryDrug DiscoveryAliphatic compoundProtecting groupChemical and Pharmaceutical Bulletin
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