Search results for "Cyanate"

showing 10 items of 210 documents

Rhenium(IV) cyanate complexes: Synthesis, crystal structures and magnetic properties of NBu4[ReBr4(OCN)(DMF)] and (NBu4)2[ReBr(OCN)2(NCO)3]

2006

Abstract Two new rhenium(IV) mononuclear compounds of formula NBu4[ReBr4(OCN)(DMF)] (1) and (NBu4)2[ReBr(OCN)2(NCO)3] (2) (NBu4 = tetrabutylammonium cation, OCN = O-bonded cyanate anion, NCO = N-bonded cyanate anion and DMF = N,N-dimethylformamide) have been synthesized and their crystal structures determined by single-crystal X-ray diffraction. 1 crystallizes in the monoclinic system with the space group P21/n, whereas 2 crystallizes in the triclinic one with P 1 ¯ as space group. In both complexes the rhenium atom is six-coordinated, in 1 by four Br atoms in the equatorial plane, and two trans-oxygen atoms, one of a DMF molecule and another one from a cyanato group, while in 2 by one brom…

ChemistryInorganic chemistrychemistry.chemical_elementCrystal structureTriclinic crystal systemRheniumCyanateMagnetic susceptibilityInorganic ChemistryCrystallographychemistry.chemical_compoundOctahedronMaterials ChemistryMoleculePhysical and Theoretical ChemistryMonoclinic crystal systemInorganica Chimica Acta
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Combination of phenolic acids and essential oils against Listeria monocytogenes

2015

Abstract Listeria monocytogenes is a psychrotrophic pathogen widely distributed in meat processing plants. Listeriosis presents very low morbidity, but very high mortality rates. Several outbreaks involving this bacterium have been reported due to the consumption of refrigerated meat and dairy products. The objective of the present study was to evaluate the in vitro antimicrobial activity of 10 phenolic acids (PAs) and 4 essential oil compounds (EOCs) as natural alternatives to control L. monocytogenes growth. The minimum inhibitory concentration (MIC) of all natural compounds was determined at pH 5, 6 and 7. The 4 most potent PAs (ρ-hydroxybenzoic acid, ferulic acid, o-coumaric acid and sy…

ChemistrySyringic acidAntimicrobialAllyl isothiocyanatemedicine.disease_causelaw.inventionFerulic acidchemistry.chemical_compoundBiochemistryListeria monocytogeneslawmedicineCarvacrolFood scienceEssential oilGeraniolFood ScienceLWT - Food Science and Technology
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Marine Isonitriles and Their Related Compounds.

2016

Marine isonitriles represent the largest group of natural products carrying the remarkable isocyanide moiety. Together with marine isothiocyanates and formamides, which originate from the same biosynthetic pathways, they offer diverse biological activities and in spite of their exotic nature they may constitute potential lead structures for pharmaceutical development. Among other biological activities, several marine isonitriles show antimalarial, antitubercular, antifouling and antiplasmodial effects. In contrast to terrestrial isonitriles, which are mostly derived from α-amino acids, the vast majority of marine representatives are of terpenoid origin. An overview of all known marine isoni…

ChinaisothiocyanatesMagnetic Resonance SpectroscopyStereochemistrycarbonimidic dichloridesmalariaPharmaceutical ScienceReviewBiology010402 general chemistry01 natural sciencesantibioticsStructure-Activity RelationshipDrug DiscoveryOrganic chemistryHumansSeawaterPharmacology Toxicology and Pharmaceutics (miscellaneous)lcsh:QH301-705.5isonitriles010405 organic chemistryTerpenesmarine natural productsformamides0104 chemical scienceslcsh:Biology (General)Marine drugs
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Synthese von 2-Acyloxy- und 2-Alkyloxy-3-ketoglycalen und ihren Bromaddukten

1983

Die an den Hydroxygruppen acetyl-, pivaloyl- und methylgeschutzten 2-Hydroxy-3-ketoglycale 5a, 5b bzw. 11 werden durch Oxidation der entsprechenden 1-O-Acylglucopyranosen 3a, 3b bzw. 9 an der freien 3-Hydroxygruppe mit Dimethylsulfoxid/Acetanhydrid oder Chlorsulfonylisocyanat hergestellt und charakterisiert. Nur beim Acetylderivat 3a verlaufen die Oxidation und die Eliminierung des 1-Acetyloxysubstituenten in einem Schritt. Beim Pivaloylderivat 3b und beim Methylderivat 9 mus die Eliminierung aus der 3-Ulose 4 bzw. 10 mit Diazabicycloundecen (DBU) vervollstandigt werden. – Die geschutzten Hex-1-enopyran-3-ulosen 5a, 5b und 11 addieren Brom stereoselektiv unter Bildung der D-ribo-konfigurier…

Chlorosulfonyl isocyanateAnomerBromineDimethyl sulfoxideStereochemistryOrganic ChemistrySubstituentchemistry.chemical_elementAdductchemistry.chemical_compoundAcetic anhydridechemistryAcetyl derivativePhysical and Theoretical ChemistryLiebigs Annalen der Chemie
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Diversity-Oriented Synthesis of Highly Functionalized Alicycles across Dipolar Cycloaddition/Metathesis Reaction

2021

AbstractThis Account gives an insight into the selective functionalization of some readily available commercial cyclodienes across simple chemical transformations into functionalized small-molecular scaffolds. The syntheses involved selective cycloadditions, followed by ring-opening metathesis (ROM) of the resulting azetidin-2-one derivatives or isoxazoline frameworks and selective cross metathesis (CM) by discrimination of the C=C bonds on the alkenylated heterocycles. The CM protocols have been described when investigated under various conditions with the purpose on exploring chemodifferentiation of the olefin bonds and a study on the access of the corresponding functionalized β-lactam or…

Chlorosulfonyl isocyanateOlefin fiberNitrile010405 organic chemistryChemistryOrganic Chemistry010402 general chemistryOrganofluorine chemistryMetathesis01 natural sciencesCombinatorial chemistryCycloaddition0104 chemical scienceschemistry.chemical_compoundSalt metathesis reactionCycloalkeneSynlett
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Regio- and stereoselective synthesis of the enantiomers of monoterpene-based β-amino acid derivatives

2007

Abstract The regio- and stereospecific addition of chlorosulfonyl isocyanate to cis-δ-pinene enantiomers has furnished monoterpene-fused β-lactams. The observed regioselectivity can be explained by ab initio DFT modeling of transition state structures. In contrast with the less reactive α-pinane-fused β-lactam 4, the resulting β-lactams 5 and 13 containing an amino group connected to a secondary carbon possess similar reactivity to the cycloalkane-fused analogues and can be easily converted to the β-amino acid and its protected derivatives. The base-catalyzed isomerization of the cis-amino ester afforded the corresponding trans-amino ester in moderate yield.

Chlorosulfonyl isocyanatechemistry.chemical_classificationChemistryStereochemistryOrganic ChemistryRegioselectivityCatalysisAmino acidInorganic Chemistrychemistry.chemical_compoundStereospecificityReactivity (chemistry)StereoselectivityPhysical and Theoretical ChemistryEnantiomerIsomerizationTetrahedron: Asymmetry
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Preferential solvation of a dicyanate ester monomer and poly(sulfone) in different organic solvents by size-exclusion chromatography.

2002

Preferential solvation parameters A in the ternary systems solvent (1) -monomer (2) -polymer (3) were determined as a tool to measure the compatibility between the cyanate ester monomer Arocy B10 and poly(sulfone), PSF, in the presence of three organic solvents: tetrahydrofuran, dimethylformamide and dicloromethane. The A parameter was measured by size-exclusion chromatography at different monomer-to-polymer ratios. The quantitative evaluation was rigorously made at polymer-diluted conditions. PSF was found to be preferentially solvated by the monomer. Concerning the solvent used, systems containing tetrahydrofuran showed the strongest solvation, the lowest A values being those obtained in …

ChromatographyPolymersViscosityIntrinsic viscosityOrganic ChemistrySize-exclusion chromatographySolvationGeneral MedicineBiochemistryAnalytical ChemistrySolventGel permeation chromatographychemistry.chemical_compoundMonomerchemistrySolubilityPolymer chemistryChromatography GelSolventsDimethylformamideSulfonesTetrahydrofuranCyanatesJournal of chromatography. A
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Chemical reduction of the mycotoxin beauvericin using allyl isothiocyanate.

2011

Abstract Beauvericin (BEA) is a bioactive compound produced by the secondary metabolism of several Fusarium strains and known to have various biological activities. This study investigated the reduction of BEA present in the concentration of 25 mg/kg on a solution model (phosphate buffer saline at pH 4 and 7) and in wheat flour using allyl isothiocyanate (AITC) as a reactant. The concentration of the mycotoxin studied was evaluated using liquid chromatography coupled to the diode array detector (LC-DAD), whereas adducts formed between the BEA and AITC were examined by liquid chromatography coupled to mass spectrometry-linear ion trap (LC-MS-LIT). In solution, BEA reduction ranged from 20% t…

ChromatographyWheat flourfood and beveragesGeneral MedicineHydrogen-Ion ConcentrationToxicologyAllyl isothiocyanateBeauvericinBioactive compoundMass SpectrometryAdductchemistry.chemical_compoundchemistryChromatography detectorIsothiocyanatesDepsipeptidesIon trapMycotoxinChromatography High Pressure LiquidFood ScienceFood and chemical toxicology : an international journal published for the British Industrial Biological Research Association
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IDENTIFICATION OF LECTINS IN THE KINETIDS OFTETRAHYMENA PYRIFORMIS

1997

Previously we described lectin-like molecules in the ciliate Tetrahymena pyriformis; by application of synthetic neoglycoconjugates it is now shown that T. pyriformis contains considerable amounts of both a beta-D-glucose- and a lactose-specific lectin. No evidence for the presence of alpha-D-mannose-, alpha-D-galactose- or of alpha-L-fucose-specific lectins could be obtained. The two lectins, identified in T. pyriformis, are associated with the kinetids. During cell division the lectins disappear or become masked in the fission furrow. Therefore, we assume that these lectins are involved in the organization of the distribution pattern of the kinetids during cell division perhaps due to lec…

CiliateCell divisionbiologyTetrahymena pyriformisLectinCell BiologyGeneral Medicinebiology.organism_classificationCell biologyMicroscopy FluorescenceAlbuminsLectinsDistribution patternTetrahymena pyriformisbiology.proteinAnimalsIdentification (biology)GlycoconjugatesCell DivisionFluorescein-5-isothiocyanateCell Biology International
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Formation of a novel ferromagnetic end-to-end cyanate bridged homochiral helical copper(ii) Schiff base complex via spontaneous symmetry breaking

2014

A homochiral helical coordination polymer of copper(II) has been synthesized using achiral precursors via spontaneous symmetry breaking and has been confirmed by single crystal X-ray diffraction and solid-state CD spectroscopy. The variable temperature magnetic measurements indicate the presence of weak ferromagnetic exchange interactions mediated by end-to-end cyanate bridges (J = +0.12 cm(-1)).

Circular dichroismSchiff baseStereochemistryChemistryCoordination polymerSpontaneous symmetry breakingchemistry.chemical_elementcircular dichroism spectroscopyCyanateferromagnetismsingle crystalsCopperX-ray diffractionInorganic ChemistryCrystallographychemistry.chemical_compoundfunctional groupsFerromagnetismcopperferromagnetic materialsta116Single crystalDalton Transactions
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