Search results for "Chemical Synthesis"

showing 10 items of 285 documents

Spin Switching with Triazolate-Strapped Ferrous Porphyrins

2019

Fe(III) porphyrins bridged with 1,2,3-triazole ligands were synthesized. Upon deprotonation, the triazolate ion coordinates to the Fe(III) ion, forming an overall neutral high-spin Fe(III) porphyrin in which the triazolate serves both as an axial ligand and as the counterion. The second axial coordination site is activated for coordination and binds p-methoxypyridine, forming a six-coordinate low-spin complex. Upon addition of a phenylazopyridine as a photodissociable ligand, the spin state of the complex can be reversibly switched with ultraviolet and visible light. The system provides the basis for the development of switchable catalase- and peroxidase-type catalysts and molecular spin sw…

chemistry.chemical_classificationkemiallinen synteesiSpin states010405 organic chemistryLigandkompleksiyhdisteet010402 general chemistry01 natural sciencesPorphyrin0104 chemical sciencesIonCatalysisInorganic Chemistrychemistry.chemical_compoundCrystallographyDeprotonationchemistrycoordination complexesPhysical and Theoretical ChemistryCounterionta116chemical synthesisVisible spectrumInorganic Chemistry
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Cyclocondensation of alpha-aminonitriles and enones: a short access to 3,4-dihydro-2H-pyrrole 2-carbonitriles and 2,3,5-trisubstituted pyrroles.

2009

The reaction of alpha,beta-unsaturated carbonyl compounds with aminoacetonitrile hydrochloride furnishes 3,5-disubstituted 3,4-dihydro-2H-pyrrole-2-carbonitriles in a one-pot reaction sequence. While these products can serve as starting materials for the preparation of polysubstituted pyrrolizidines, they are kinetically stable against the base-induced elimination of HCN. In contrast, their 2-substituted analogues obtained from alpha-substituted alpha-aminonitriles can be readily converted to the corresponding 2,3,5-trisubstituted pyrroles under microwave irradiation. The key step presumably involves the thermal electrocyclization of a stabilized 2-azapentadienyl anion formed by condensatio…

chemistry.chemical_compoundDeprotonationElectrocyclic reactionchemistryNitrileHydrochlorideOrganic ChemistryOrganic chemistryCondensation reactionChemical synthesisEnonePyrroleThe Journal of organic chemistry
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Microwave-Assisted Synthesis of Polysubstituted 4-Quinolones from Deprotonated α-Aminonitriles

2010

The α-alkylation of deprotonated N-aryl-α-aminonitriles with α-bromoesters furnishes intermediates that can be cyclized to 4-quinolones upon microwave irradiation. Alternatively, base-induced dehydrocyanation of the alkylation products furnishes enaminoesters, which can, for example, be converted into quinoline-3-carboxylates.

chemistry.chemical_compoundDeprotonationMicrowave chemistryChemistryOrganic Chemistry4-quinolonesMicrowave irradiationCarboxylatePhysical and Theoretical ChemistryAlkylationPhotochemistryChemical synthesisMicrowaveEuropean Journal of Organic Chemistry
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Competing Ring-Photoisomerization Pathways in the 1,2,4-Oxadiazole Series. An Unprecedented Ring-Degenerate Photoisomerization

2002

The irradiation of some 5-alkyl-3-amino-1,2,4-oxadiazoles at lambda = 254 nm in methanol in the presence of triethylamine (TEA) gave ring-photoisomerization both into 2-alkyl-5-amino-1,3,4-oxadiazoles and, unprecedently, into the ring-degenerate 3-alkyl-5-amino-1,2,4-oxadiazoles. The competing ring contraction-ring expansion route and the internal cyclization-isomerization mechanism explain the results.

chemistry.chemical_compoundReaction mechanismchemistryPhotoisomerizationOrganic ChemistryOxadiazoleMethanolRing (chemistry)PhotochemistryTriethylamineIsomerizationChemical synthesisThe Journal of Organic Chemistry
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Wide Rim Urethanes Derived from Calix[4]arenes:  Synthesis and Self-Assembly

2006

[reaction: see text] Calix[4]arenes 4, substituted at the wide rim by four N-tolyl-urethane groups, were synthesized, as well as derivatives 10a,b bearing two or three tolyl-urea groups beside of one or two urethane group(s). In contrast to tetra-tolyl urea 11, the urethane derivatives do not form hydrogen-bonded, dimeric capsules in CDCl3 or benzene-d6, but the dimerization can be induced for the triurea 10b by tetraethylammonium cations as guests. The quantitative formation of heterodimers is observed for all urethanes 4 and 10a,bin benzene-d6 in mixtures with a "tetra-loop" tetraurea 14, while "bisloop" tetraureas 13 require di- or triurea derivatives 10a,b for a clean heterodimerization.

chemistry.chemical_compoundTetraethylammoniumStereochemistryChemistryHydrogen bondDimerOrganic ChemistryPolymer chemistryCalixareneUreaSelf-assemblyChemical synthesisInclusion compoundThe Journal of Organic Chemistry
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Synthesis and structural characterization of cis- and trans-fused 4a,5,6,7,8,8a-hexahydro-2H,4H-1,3-benzodithiines and their 2-methyl and 2,2-dimethy…

2002

Both cis- and trans-fused 4a,5,6,7,8,8a-hexahydro-2H,4H-1,3-benzodithiine together with their 2-methyl and 2,2-dimethyl derivatives were prepared as racemates from the appropriate dithiols obtained via multistep syntheses. The products were characterized by 1 H and 13 C NMR, mass spectrometry, and for two of the cis-fused compounds by X-ray diffraction. 1 H, 1 H vicinal coupling constants indicated that all compounds attain chair-chair conformations as their predominant conformations. All three trans-fused isomers exist in totally biased chair-chair conformations and are essentially conformationally locked, whereas the cis-fused compounds are conformationally mobile and can potentially atta…

chemistry.chemical_compoundchemistryBicyclic moleculeStereochemistryOrganic ChemistryX-ray crystallographyDithiolMoleculeCarbon-13 NMRChemical synthesisConformational isomerismCis–trans isomerismThe Journal of organic chemistry
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Convenient Synthesis of 3-Cinnamoyl-2-styrylchromones: Reinvestigation of the Baker-Venkataraman Rearrangement

2010

An efficient and straightforward, one-pot sequence gives access to highly functionalized 3-cinnamoyl-2-styrylchromones in excellent yields. The low solubility of the target molecules allows convenient isolation. The formation of an α,α-dicinnamoylated acetophenone, as a consequence of a two-fold Baker-Venkataraman sequence, has to be anticipated.

chemistry.chemical_compoundchemistryOne pot reactionOrganic ChemistryBaker–Venkataraman rearrangementMoleculeOrganic chemistrySequence (biology)Physical and Theoretical ChemistrySolubilityCombinatorial chemistryChemical synthesisAcetophenoneEuropean Journal of Organic Chemistry
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Sulfur-incorporating cyclotriveratrylene analogues: the synthesis of cyclotrithioguaiacylene.

2011

Cyclotriguaiacylene 1 is the universal precursor of cryptophanes, and represents an important intermediate for the preparation of functionalized cavitands of the cyclotriveratrylene family. Its thio analogue (cyclotrithioguaiacylene 3) was synthesized by two different routes, involving either the Newman-Kwart or the Pummerer rearrangement. The latter, performed starting from a trisulfoxide precursor, produced a purer compound in higher overall yield.

chemistry.chemical_compoundchemistryPummerer rearrangementYield (chemistry)Organic ChemistryCavitandThio-Organic chemistryCyclotriveratryleneChemical synthesisCryptophaneInclusion compoundThe Journal of organic chemistry
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Synthesis and characterization of perfluoroalkyl-pyrenes embedded in a polymethylmethacrylate matrix

2012

fluorinated molecules pyrene PMMA photochemical synthesis structural characterization photoluminescence
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Rod–coil copolymers from oligo(p-benzamide) foldamers

2007

Self assembling rod–coil copolymers were synthesized in which oligo(p-benzamide) rods up to the octamer were prepared via iterative solution synthesis employing the acid labile 2,4-dimethoxybenzyl amide protective group.

genetic structuresGeneral ChemistrySolution synthesisChemical synthesischemistry.chemical_compoundAcid labilechemistryAmidePolymer chemistryMaterials ChemistryCopolymersense organsHistone octamerSelf-assemblyBenzamideJ. Mater. Chem.
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