Search results for "Reaction"

showing 10 items of 6134 documents

Asymmetric Synthesis of Monofluorinated 1-Amino-1,2-dihydronaphthalene and 1,3-Amino Alcohol Derivatives.

2016

Enantioenriched 1-amino-4-fluoro-1,2-dihydronaphthalene derivatives are accessed via two complementary synthetic strategies. The careful optimization of the reaction conditions required for the elimination step in one route has allowed both the identification of an anchimerically assisted reaction pathway and, more importantly, access to a divergent reaction pathway toward fluorinated 1,3-amino alcohols from a common intermediate just by adjusting the number of equivalents of base used.

Reaction conditionschemistry.chemical_compound010405 organic chemistryStereochemistryChemistryOrganic ChemistryEnantioselective synthesisAlcoholPhysical and Theoretical Chemistry010402 general chemistry01 natural sciencesBiochemistry0104 chemical sciencesOrganic letters
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ChemInform Abstract: 3,4-Dihydro-2H-pyrrole-2-carbonitriles: Useful Intermediates in the Synthesis of Fused Pyrroles and 2,2′-Bipyrroles.

2016

Various heterocyclic structures containing the pyrrole moiety have been synthesized from easily accessible 3,4-dihydro-2H-pyrrole-2-carbonitriles in one-pot procedures. 5,6,7,8-Tetrahydroindolizines, 2,3-dihydro-1H-pyrrolizines as well as 6,7,8,9-tetrahydro-5H-pyrrolo[1,2-a]azepines were obtained from these precursors in high yields in an alkylation/annulation sequence. The same conditions were applied in the synthesis of a 5,8-dihydroindolizine, which could easily be transformed to the corresponding indolizine by dehydrogenation. Furthermore, oxidative couplings of 3,4-dihydro-2H-pyrrole-2-carbonitriles with copper(II)-salts furnished 2,2′-bipyrroles as well as 5,5′-bis(5-cyano-1-pyrroline…

Reaction conditionschemistry.chemical_compoundAnnulationchemistryMoietychemistry.chemical_elementIndolizineDehydrogenationGeneral MedicineAlkylationCombinatorial chemistryCopperPyrroleChemInform
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ChemInform Abstract: Asymmetric Synthesis of Monofluorinated 1-Amino-1,2-dihydronaphthalene and 1,3-Amino Alcohol Derivatives.

2016

Enantioenriched 1-amino-4-fluoro-1,2-dihydronaphthalene derivatives are accessed via two complementary synthetic strategies. The careful optimization of the reaction conditions required for the elimination step in one route has allowed both the identification of an anchimerically assisted reaction pathway and, more importantly, access to a divergent reaction pathway toward fluorinated 1,3-amino alcohols from a common intermediate just by adjusting the number of equivalents of base used.

Reaction conditionschemistry.chemical_compoundChemistryEnantioselective synthesisAlcoholGeneral MedicineBase (exponentiation)Combinatorial chemistryChemInform
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A study of the behaviour of 2,4-substituted thiosemicarbazides toward orthoesters: Formation of mesoionic compounds

1997

The reactions beetwen 2,4-disubstituted thiosemicarbazides and orthoesters in refluxing xylene led to the formation of the 1,2,4-triazoline-5-thione ring and to the 1,2,4-triazolium-5-thiolate ring. The formation of the mesoionic componds is due to rearrangement of the easily available 2,4-disubstituted thiosemicarbazides to 1,4-disubstituted thiosemicarbazides under the reaction conditions adopted. This method can be usefully used for the synthesis of mesoionic compounds, especially in the case of the 2-methyl-4-phenylthiosemicarbazide.

Reaction conditionschemistry.chemical_compoundChemistryOrganic ChemistryXyleneMesoionicRing (chemistry)Medicinal chemistryJournal of Heterocyclic Chemistry
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Reductive cleavage of 2,2,2-trichloroethyl esters with sodium telluride

1998

Abstract Carboxylic acids are regenerated from their 2,2,2-trichloroethyl esters by treatment with sodium telluride in dimethylformamide in smooth conditions and with good yields. The reaction conditions are compatible with other functional and protective groups such as methyl ester, acetate or tert-butyldimethylsilyl ethers.

Reaction conditionschemistry.chemical_compoundChemistryReductive cleavageOrganic ChemistrySodium tellurideOrganic chemistryDimethylformamide
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Highly stable Cp*-Ir(III) complexes with N-heterocyclic carbene ligands as C-H activation catalysts for the deuteration of organic molecules.

2006

The preparation of a series of complexes of the type CpIrX2(NHC) provides effective catalysts for the H/D exchange of a wide range of organic molecules in methanol-d4. The reaction proceeds with higher yields under milder reaction conditions than previous CpIr systems reported thus far. For comparative purposes, we also studied the catalytic activity of CpIrCl2(PMe3) under the same reaction conditions. The molecular structures of two of the new CpIr(NHC) complexes are described.

Reaction conditionschemistry.chemical_compoundColloid and Surface ChemistryChemistryStereochemistryGeneral ChemistryBiochemistryMedicinal chemistryCarbeneCatalysisCatalysisOrganic moleculesJournal of the American Chemical Society
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Synthesis of Macropolycyclic Ligands Based on Tetraazacycloalkanes

1998

A versatile synthesis of spherical macrobicyclic and cylindrical macrotricyclic ligands is described using 1,4,8,11-tetraazacyclotetradecane (cyclam), 1,4,7,10-tetraazacyclododecane (cyclen), or dioxo macrocycles as precursors. Macrobicycles have been obtained by allowing cyclam, cyclen, or 5,12-dioxocyclam (1,4,8,11-tetraazacyclotetradecane-5,12-dione) to react with a bis-electrophilic spacer under high dilution conditions. A surprising selectivity has been observed for 2,6-dioxocyclen (1,4,7,10-tetraazacyclododecane-2,6-dione), which yields only macrotricycles under the same reaction conditions. Molecular modelling studies have been carried out to investigate the selectivity of the reacti…

Reaction conditionschemistry.chemical_compoundCyclenChemistryStereochemistryOrganic ChemistryCyclamRigid structureProtonationPhysical and Theoretical ChemistrySelectivityCombinatorial chemistryEuropean Journal of Organic Chemistry
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Änderung der polymerisationsaktivität und der zahl aktiver zentren bei der alterung der katalysatorsysteme Al(C2H5)3/TiCl3 und Al(C2H5)2Cl/TiCl3. Zur…

1965

Es wird das Alterungsverhalten der Katalysatorsysteme Al(C2H5)3/TiCl3 und Al(C2H5)2Cl/TiCl3 untersucht; an den drei Monomeren Athylen, Propylen und Buten-1 wird die Anderung der Polymerisationsaktivitat in Abhangigkeit vom Al/Ti-Verhaltnis fur verschiedene Alterungszeiten des Gesamtkatalysators gemessen. Nach anfanglichem Anstieg zeigt sich ein mehr oder weniger starker Abfall der Polymerisationsaktivitat mit steigender Alterungszeit und wachsendem Al/Ti-Verhaltnis. Die Aktivitatsanderung ist unter vergleichbaren Bedingungen fur die drei Monomeren verschieden. Daraus wird auf das Vorhandensein verschieden aktiver Zentren fur die Polymerisation der Monomeren geschlossen. The aging of the cat…

Reaction conditionschemistry.chemical_compoundMonomerEthylenePolymerizationChemistryPolymer chemistryCatalysisDie Makromolekulare Chemie
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Eine methode zur untersuchung der polymerisation von äthylen und gasförmigen α-olefinen bei normaldruck. Zur polymerisation mit metallorganischen mis…

1963

Es wird eine einfache Apparatur zur Messung des Reaktionsverlaufs bei der Polymerisation gasformiger Monomerer beschrieben. In einem geschlossenen System wird der Verbrauch des Monomeren volumetrisch verfolgt. Der Einflus verschiedener Reaktionsbedingungen auf die Polymerisation von α-Olefinen mit metallorganischen Mischkatalysatoren wird diskutiert. Die Methode bietet eine gute Reproduzierbarkeit und weist eine Fehlerbreite von maximal ± 4% auf. A simple apparatus to measuring the course of the polymerization of gaseous monomers is described; the consumption of the monomer is measured volumetrically in a closed system. Influence and variation of reaction conditions on the polymerization of…

Reaction conditionschemistry.chemical_compoundMonomerchemistryPolymerizationPolymer chemistryDie Makromolekulare Chemie
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Anodic Oxidation as an Enabling Tool for the Synthesis of Natural Products

2020

Electrochemistry provides a valuable toolbox for organic synthesis and offers an appealing, environmentally benign alternative to the use of stoichiometric quantities of chemical oxidants or reductants. Its potential to control current efficiency along with providing alternative reaction conditions in a classical sense makes electrochemistry a suitable method for large-scale industrial transformations as well as for laboratory applications in the synthesis of complex molecular architectures. Even though research in this field has intensified over the recent decades, many synthetic chemists still hesitate to add electroorganic reactions to their standard repertoire, and hence, the full poten…

Reaction conditionschemistry.chemical_compoundNatural productchemistryAnodic oxidationOrganic ChemistryNanotechnologyOrganic synthesisBond formationElectrochemistryCatalysisSynthesis
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