Search results for "ethylamine"

showing 10 items of 230 documents

ChemInform Abstract: New Conditions for the Generation of Dianions of Carboxylic Acids.

2010

Abstract Lithium carboxylic acid enediolates are generated efficiently using lithium amides prepared from thienyllithium or butyllithium and either diethylamine, piperazine, N,N′-dibenzylethylenediamine, N-benzylpiperazine or 1,3,3-trimethyl-6-azabicyclo[3.2.1]octane, even in catalytic amounts.

chemistry.chemical_classificationDiethylaminechemistry.chemical_compoundPiperazinechemistryCarboxylic acidButyllithiumchemistry.chemical_elementLithiumGeneral MedicineMedicinal chemistryCatalysisOctaneChemInform
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Synthese von geschützten Asparagin-Glycopeptiden durch N-terminale Peptidketten- Verlängerung. _ Teilsequenzen der Rinder-Desoxyribonuclease A und de…

1983

N-[2-(Triphenylphosphonio)ethoxycarbonyl] -[Peoc-]asparaginsaure-benzylester (8h) und -tert-butylester (8i) werden mit 2-Acetamido-3,4,6-tri-O-acetyl-2-desoxy-β -D-glucopyranosylamin (2) zu den N4-Glycosylasparagin-Derivaten 19 verknupft. Aus diesen kann die Peoc-Gruppe selektiv mit Diethylamin/tert-Butylalkohol oder Morpholin/Methylendichlorid abgespalten werden, wobei in den entstandenen N4-Glycosylasparaginestern 22 alle anderen Schutzgruppen und die glycosidische Bindung erhalten bleiben. Durch Kondensation von 22 mit Peoc-Aminosauren 8 entstehen die voll geschutzten N4-Glycosylasparagin-Dipetide 24 und 30. Bei Kondensation der N2 deblockierten N4-Glycosylasparaginester 22 mit den Peoc-…

chemistry.chemical_classificationDiethylaminechemistry.chemical_compoundchemistryDeoxyribonuclease AStereochemistryMorpholineOrganic ChemistryAspartic acidPeptideGlycosidic bondPhysical and Theoretical ChemistryAmino acidLiebigs Annalen der Chemie
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Das System 2‐Halogenethylester/Cholinester als Zweistufen‐Schutzgruppe für die Carboxylfunktion von Aminosäuren und Peptiden

1979

Das System 2-Chlorethyl- und 2-Bromethylester/Cholinester wird als Carbonsaure-Schutzfunktion beschrieben. Die 2-Chlorethyl-(OEt(Cl))- und die 2-Bromethylester (OEt(Br)) der Aminosauren (4) lassen sich einfach herstellen und mit Z- und Boc-Aminosauren zu Z- und Boc-Dipeptidestern 5 und 6 verknupfen. Die Esterfunktionen sind gegen nicht zu stark saure und basische Einflusse bestandig. Sie konnen mit Natriumiodid in DMF in 2-Iodethylester 8 ubergefuhrt werden, welche mit Zink in einer Eintopfreaktion spaltbar sind. Durch Umsetzung mit Trimethylamin gehen die hydrophoben 2-Halogenethylester in die hydrophilen Cholinester 10 und 11 uber. Diese sind sehr stabil gegen Sauren. Sie konnen in wasrig…

chemistry.chemical_classificationDipeptideStereochemistryCarboxylic acidchemistry.chemical_elementTrimethylamineZincAmino acidInorganic Chemistrychemistry.chemical_compoundchemistrySodium iodideCholineRacemizationChemische Berichte
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Synthèse de chalcones à base de tétrathiafulvalène: RC(O)CHC(CH3)TTF, TTFC(O)CHC(CH3)R (R  TTF: C6H3S4; Bct: C6H5Cr(CO)3; Fc: C5H4FeC5H5). Propr…

1992

Abstract Novel chalcones that contain tetrathiafulvalene (TTF) and/or metallocene (ferrocenyl or benchrotrenyl) moieties: RC(O)CHC(CH 3 )R′ (R and/or R′  TTF: C 6 H 3 S 4 ; Fc: C 5 H 4 FeC 5 H 5 ; Bct: C 6 H 5 Cr(CO) 3 ) were prepared using TiCl 3 /Et 3 N as the condensation reagent. The 1-1 charge transfer complex with TCNQ (tetracyanoquinodimethane was obtained for the ditetrathiafulvalenic derivative (R  R′ TTF). This complex exhibits the semiconducting behaviour.

chemistry.chemical_classificationKetoneStereochemistryOrganic ChemistryCondensation reactionCharge-transfer complexBiochemistryMedicinal chemistryTetracyanoquinodimethaneInorganic Chemistrychemistry.chemical_compoundchemistryMaterials ChemistryBenzophenonePhysical and Theoretical ChemistryTriethylamineMetalloceneTetrathiafulvaleneJournal of Organometallic Chemistry
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Chemical recycling of polyenaminones by transamination reaction via amino–enaminone polymerisation/depolymerisation

2019

Abstract Novel oligo- and polyenaminones with Mw ∼ 3000 Da were prepared in excellent yields by amino–enaminone ‘click’ polymerisation of 1,3- and 1,4-bis[3-(dimethylamino)acryloyl]arenes with 1,3- and 1,4-phenylenediamine. The obtained oligomers and polymers were depolymerised quantitatively to the starting bis-enaminones and diamines by treatment with excess dimethylamine in ethanol at 50 °C. This simple polymerisation/depolymerisation method allows for a closed-loop recycling of polyenaminone-based materials. UV light absorbance at wavelengths below 470 nm indicates promising optical properties of these polymers.

chemistry.chemical_classificationLight absorbanceEthanolPolymers and PlasticsTransaminationOrganic ChemistryGeneral Physics and Astronomy02 engineering and technologyPolymer010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciences0104 chemical scienceschemistry.chemical_compoundchemistryPolymerizationMaterials Chemistry0210 nano-technologyDimethylamineEuropean Polymer Journal
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Dienediolates of unsaturated carboxylic acids in synthesis. Aldehydes and ketones from alkyl halides, by ozonolysis of β,γ-unsaturated α-alkyl carbox…

1997

Abstract A convenient two-step procedure for a two carbon homologative conversion of alkyl halides into aldehydes and methyl ketones by α-alkylation of unsaturated carboxylic acids, followed by ozonolysis is developed and applied to the synthesis of ω-chloro aldehydes. Triethylamine is superior to dimethyl sulfide or triphenylphosphine for cleavage of the ozonides, except when aldol condensation side reactions require use of protic solvents and iodide salts. Cleavage of the ozonides by triethylamine is shown to occur mainly through a reductive process.

chemistry.chemical_classificationOzonolysisTertiary amineOrganic ChemistryIodideHalideBiochemistrychemistry.chemical_compoundchemistryDrug DiscoveryOrganic chemistryAldol condensationTriphenylphosphineTriethylamineAlkylTetrahedron
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A new macrocyclic dipyrazolate salt of diazatetraester structure able to efficiently and selectively interact with psychotropic phenethylammonium sal…

2002

Abstract The equilibrium stability constants (Ks) of a series of ammonium pyrazolate complexes [L22−]2RN(R′)H2+ (7, R′=H and 8, R′=Me) formed from a new macrocyclic disodium dipyrazolate salt of diazatetraester structure 6[L22−] 2Na+ and ammonium salts [RNH3+X− or RN(Me)H2+X−] of psychotropic drugs and neurotransmitter catecholamines has been evaluated by electrochemical methods in DMSO solution. The resulting Ks values demonstrate that in general, the diazatetraester crown-derived dipyrazolate salt 6 exerts a stronger complexing effect over phenethylammonium ions than that of the dioxatetraester crown-derived disodium dipyrazolate salt 2 previously reported. Interestingly, complexes formed…

chemistry.chemical_classificationPhenethylamineStereochemistryOrganic ChemistrySubstituentSalt (chemistry)General ChemistryElectrochemistryMedicinal chemistryIonInorganic Chemistrychemistry.chemical_compoundchemistryEquilibrium stabilityMaterials ChemistryAmmoniumJournal of Supramolecular Chemistry
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Effective complexation of psychotropic phenethylammonium salts from a disodium dipyrazolate salt of macrocyclic structure

2002

The equilibrium stability constants (Ks) of ammonium pyrazolate complexes [L2−]2RN(R′)H2+ (3, R′ = H and 4, R′ = Me) formed from a macrocyclic disodium dipyrazolate salt 2[L2−] 2Na+ and ammonium salts (RNH3+X− or RN(Me)H2+X−) of psychotropic drugs and neurotransmitter catecholamines have been evaluated by electrochemical methods in DMSO solution. The resulting Ks values demonstrate that, except for (±)-amphetamine, the complexes formed by lipophilic primary [mescaline, (+)-amphetamine, (±)-p-methoxyamphetamine (PMA), (±)-3,4-methylenedioxyamphetamine (MDA)] and secondary [(±)-methamphetamine, (+)-methamphetamine and (±)-3,4-methylenedioxymethamphetamine (MDMA ‘ecstasy’)] phenethylamines are…

chemistry.chemical_classificationStereochemistrySalt (chemistry)PhenethylaminesMescalineCarbon-13 NMRElectrochemistryMedicinal chemistrychemistry.chemical_compoundchemistryEquilibrium stabilitymedicineAmmoniummedicine.drugJ. Chem. Soc., Perkin Trans. 2
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Photoinduced molecular rearrangements. Some comments on the ring-photoisomerization of 1,2,4-oxadiazoles into 1,3,4-oxadiazoles

2001

The ring-photoisomerization of 3-amino- and 3-methylamino-5-phenyl-1,2,4-oxadiazoles into the corresponding 2-amino- and 2-methylamino-5-phenyl-1,3,4-oxadiazoles has been reinvestigated by examining the effect of a base on the photoreaction. On irradiating at λ = 254 nm in methanol, yields of the ring-photoisomers were found to be significantly enhanced by the addition of triethylamine (TEA) in the photoreaction medium. By contrast, irradiation of the 3-amino-5-phenyloxadiazole in acetonitrile containing TEA gave an almost complete photoreduction into benzoylguanidine, while few percent of the ring photoisomer were detected. Furthermore, the pyrene-sensitized photolysis of 3-amino-5-phenylo…

chemistry.chemical_classificationchemistry.chemical_compoundBase (chemistry)PhotoisomerizationChemistryOrganic ChemistryPhotodissociationIrradiationMethanolRing (chemistry)PhotochemistryAcetonitrileTriethylamineJournal of Heterocyclic Chemistry
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ChemInform Abstract: Palladium-Catalyzed Synthesis of Mono- and Diphosphorylated 1,10-Phenanthrolines.

2013

A general protocol for the coupling of mono- and dihalo-1,10-phenanthrolines with diethyl phosphite is reported. This reaction proceeds smoothly in the presence of a Pd(OAc)2/dppf catalytic system and triethylamine as a base.

chemistry.chemical_classificationchemistry.chemical_compoundBase (chemistry)chemistryOrganic chemistrychemistry.chemical_elementGeneral MedicineMedicinal chemistryTriethylamineCatalysisPalladiumChemInform
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