Search results for "double bond"

showing 10 items of 184 documents

Synthesis of plagiochiline N from santonin.

2001

This article reports the transformation of O-acetylisophotosantonin, obtained by photochemical rearrangement of santonin, into plagiochiline N, an ent-2,3-secoaromadendrane isolated from Plagiochila ovalifolia. The synthesis was carried out in a sequence involving as the key steps (a) the substitution of the lactone moiety by a gem-dimethylcyclopropane ring through a synthetic intermediate having a C(6)-C(7) double bond and (b) the ozonolysis of the C(2)-C(3) bond followed by cyclization to the dihydropyran ring characteristic of plagiochiline N. Spectroscopic data of the synthetic product fully coincided with the reported data for the natural product.

chemistry.chemical_classificationNatural productOzonolysisPlants MedicinalDouble bondDihydropyranStereochemistryAntinematodal AgentsOrganic ChemistryAlkenesRing (chemistry)chemistry.chemical_compoundchemistryMoietySantoninLactoneThiocyanatesSantoninThe Journal of organic chemistry
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Fluorinated Heterocyclic Compounds. An Expedient Route to 5-Perfluoroalkyl-1,2,4-triazoles via an Unusual Hydrazinolysis of 5-Perfluoroalkyl-1,2,4-ox…

2003

The hydrazinolysis reaction of 5-perfluoroalkyl-1,2,4-oxadiazoles has been investigated. Nucleophilic addition of the reagent to the C(5)-N(4) double bond of the oxadiazole ring, followed by ring-opening and then ring-closure involving the beta-nitrogen atom of the hydrazino moiety and the C(3) of the oxadiazole ring, explains the formation of 5-perfluoroalkyl-1,2,4-triazoles as final products. Useful applications in synthesis of this uncommon hydrazinolysis can be claimed.

chemistry.chemical_classificationNucleophilic additionDouble bondOrganic ChemistryHydrazineOxadiazoleGeneral MedicineRing (chemistry)Medicinal chemistryChemical synthesischemistry.chemical_compoundchemistryReagentTriazole derivativesOrganic chemistryMoietyThe Journal of Organic Chemistry
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Reactivity of the carbon-carbon double bond towards nucleophilic additions. A dft analysis

2004

Abstract The global and local electrophilicity indexes have been used to characterize the reactivity pattern of the CC double bond towards nucleophilic addition reactions. A wide family of molecules including ketones, esters, anhydrides, nitriles and nitrocompounds containing appropriate substitution on the CC double bond have been classified within an unique scale of reactivity. The predictive capability of the theoretical model is tested against a series of benzylidenemalononitriles and substituted α-nitrostilbenes.

chemistry.chemical_classificationNucleophilic additionDouble bondOrganic ChemistryReinforced carbon–carbonBiochemistrychemistryNucleophileComputational chemistryDrug DiscoveryElectrophileOrganic chemistryMoleculeDensity functional theoryReactivity (chemistry)
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Revisiting the photochemical synthesis of [FeFe]-hydrogenase mimics: reaction optimization, mechanistic study and electrochemical behaviour

2020

The photoreaction of [(μ-S)2Fe2(CO)6] and alkenes or alkynes has been optimized to readily obtain functionalized [FeFe]-hydrogenase mimics. Irradiation under low CO pressure in THF produces the corresponding photo-adducts in good/acceptable (alkenes/alkynes) yields, with retention of the starting olefin stereochemistry. DFT-calculations provide plausible reaction pathways in both, singlet and triplet states. The DFT-calculation based in the singlet state is energetically more favorable. The electrochemical behavior of the synthesized compounds is also presented, including studies in acidic media. The electrochemical properties of the products vary in the presence of a double bond (cycloaddi…

chemistry.chemical_classificationOlefin fiberHydrogenaseDouble bondchemistryGeneral Chemical EngineeringSingle bondGeneral ChemistrySinglet statePhotochemistryElectrochemistryCycloadditionRSC Advances
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Reactions of Piperazin-2-one, Morpholin-3-one, and Thiomorpholin-3-one with Triethyl Phosphite Prompted by Phosphoryl Chloride: Scope and Limitations

2019

The reaction of the title lactams with triethyl phosphite prompted by phosphoryl chloride provided six-membered ring heterocyclic phosphonates or bisphosphonates. These novel scaffolds might be of interest as building blocks in medicinal chemistry. The course of the reaction was dependent on the structure of the used substrate. Thus, morpholin-3-one and thiomorpholin-3-one readily provided the corresponding 1,1-bisphosphonates (compounds 1, 2, 7, 14 and 16), whereas the protection of their nitrogen atom resulted in the formation of dehydrophosphonates (compounds 5, 6, and 8). Piperazin-2-one reacted differently yielding mixture of cis- and trans- piperazine-2,3-diyl-bisphosphonates (compoun…

chemistry.chemical_classificationPhosphoryl chlorideDouble bondGeneral Chemical EngineeringSubstrate (chemistry)General ChemistryRing (chemistry)Medicinal chemistryArticlelcsh:ChemistryHydrolysischemistry.chemical_compoundNitrogen atomchemistrylcsh:QD1-999CytosineDerivative (chemistry)ACS Omega
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Flexible Synthesis of Planar Chiral Azoninones and Optically Active Indolizidinones

2014

The flexible synthesis of defined substituted optically active indolizidinones starting from chiral pool (S)-proline and trans 4-hydroxy-(S)-proline is described. Several defined 2-vinylpyrrolidines were generated in short sequences. The aza-Claisen rearrangement using chloro and phenylketene equivalents delivered nine-membered-ring lactams with up to three stereogenic centres and pS-arranged E olefins. Depending on the substitution pattern, certain azoninones had a flexible conformation and showed pS/pR double-bond flipping. Treatment of the unsaturated lactams with the soft electrophile iodine induced diastereoselective transannular ring contractions. Here, the planar chiral arrangement o…

chemistry.chemical_classificationPlanarDouble bondchemistryStereochemistryOrganic ChemistryElectrophileMoleculePhysical and Theoretical ChemistrySigmatropic reactionOptically activeRing (chemistry)StereocenterEuropean Journal of Organic Chemistry
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Hydrogen bonds in unpolar matrix — Comparison of complexation in polymeric and low molecular-weight systems

1991

By ene-reaction of 4-phenyl-1,2,4-triazoline-3,5-dione with double bonds, polar 4-phenyl-1,2,4-triazolidine-3,5-dione (phenyl urazole) groups are introduced into unpolar matrices. Hydrogen-bond complexes are formed between two amide-like units. The temperature dependence of complex formation in dilute hydrocarbon medium is obtained from remperature-dependent IR spectra in the region of the C=O stretching vibration. Results obtained for a low molecular-weight model system are compared with modified polybutadienes, where the groups are attached statistically along the polymer backbone. The enthalpy and the entropy of complex formation (ΔH f =−28.6 kJ/mol; ΔS f =−52 J/mol K−1) obtained for the…

chemistry.chemical_classificationPolymers and PlasticsDouble bondChemistryStereochemistryHydrogen bondEnthalpyInfrared spectroscopyPolymerStandard enthalpy of formationCrystallographyColloid and Surface ChemistryHydrocarbonMaterials ChemistryPhysical and Theoretical ChemistryEquilibrium constantColloid and Polymer Science
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Reactions of Maleisomides with Alcohols

2004

Abstract New surfactants (surfmers) with various amide and ester groups next to C˭C double bonds have been obtained. Maleic acid amidesters (AE) with different hydrophobic groups at the nitrogen atom and hydrophilic substituents at oxygen atoms were synthesized starting with maleic isoimides. 1H KMR and IR spectra were used for their characterization. Some were further characterized for their critical micellar concentration (CMC). A few cationic and zwitterionic surfmers were also prepared from isoimide precursors and characterized. All these surfmers were applied in batch emulsion polymerization of styrene, and in core‐shell seeded copolymerization of styrene and butylacrylate to give late…

chemistry.chemical_classificationPolymers and PlasticsDouble bondMaleic acidCationic polymerizationEmulsion polymerizationSurfaces Coatings and FilmsStyrenechemistry.chemical_compoundchemistryAmideCritical micelle concentrationPolymer chemistryCopolymerOrganic chemistryPhysical and Theoretical ChemistryJournal of Dispersion Science and Technology
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Influence of the irradiation parameters on the molecular modifications of an isotactic polypropylene gamma-irradiated under vacuum

2000

Isotactic polypropylene was irradiated under vacuum in a complete set of experimental conditions. The influence of the irradiation parameters, total absorbed dose, D, and dose rate, I, was analysed in order to verify the theoretical predictions of a simple kinetic model, already presented (Sarcinelli L, Valenza A, Spadaro G. Polymer 1997;38:2307), based on the rates of the main reactions occurring during irradiation, i.e. β-scission, addition to double bonds and termination. The concentration of free radicals and double bonds formed during irradiation is detected together with a comparison to their dependence on the irradiation parameters. A quantitative determination of the “inversion curv…

chemistry.chemical_classificationPolymers and PlasticsDouble bondStereochemistryRadicalAnalytical chemistryPolymerCondensed Matter PhysicsBranching (polymer chemistry)chemistryMechanics of MaterialsAbsorbed doseTacticityMaterials ChemistryMoleculeIrradiationPolymer Degradation and Stability
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Die alkoholyse des triethylsilans katalysiert von [(CH3)3P]2Ru(CO)2Cl2

1983

Abstract [(CH 3 ) 3 Pl 2 Ru(CO) 2 Cl 2 is an effective catalyst for the reaction of alcohols with triethylsilane. The rate of this reaction varies with the substituents in the hydroxy compound; it is fastest for short primary alcohols. Even in the presence of groups which can be hydrosilated (CC triple or double bonds, as well as ketones), a hydroxy group reacts preferably and completely with the silane. Kinetic experiments have been performed with the system Et 3 SiH/CH 3 CH(OH)COOEt/Ru complex.

chemistry.chemical_classificationPrimary (chemistry)Double bondChemistryOrganic ChemistryHydroxy groupBiochemistryMedicinal chemistrySilaneHydroxy compoundCatalysisInorganic Chemistrychemistry.chemical_compoundMaterials ChemistryOrganic chemistryPhysical and Theoretical ChemistryTriethylsilaneJournal of Organometallic Chemistry
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