Search results for " ACE"

showing 10 items of 1883 documents

CCDC 1047964: Experimental Crystal Structure Determination

2015

Related Article: Wdeson P. Barros, M. Luisa Calatayud, Francesc Lloret, Miguel Julve, Nadia Marino, Giovanni De Munno, Humberto O. Stumpf, Rafael Ruiz-García, Isabel Castro|2016|CrystEngComm|18|437|doi:10.1039/C5CE02058A

(mu2-Aqua)-(mu2-pyrazolato-NN')-bis(47-dimethyl-110-phenanthroline-NN')-di-copper(ii) diperchlorate acetonitrile solvate monohydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 651347: Experimental Crystal Structure Determination

2008

Related Article: A.Cuevas, C.Kremer, L.Suescun, S.Russi, A.W.Mombru, F.Lloret, M.Julve, J.Faus|2007|Dalton Trans.||5305|doi:10.1039/b708927a

(mu~2~-Malonato-OO'O'')-tetrachloro-bis(29-dimethyl-110-phenanthroline)-cobalt(ii)-rhenium(iv) acetonitrile solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 750190: Experimental Crystal Structure Determination

2011

Related Article: P.Albores, E.Rentschler|2010|Dalton Trans.|39|5005|doi:10.1039/b925214b

(mu~3~-Oxo)-pentakis(mu~2~-22-dimethylpropanoato-OO')-aqua-(22'-bipyridine-NN')-(22-dimethylpropanoato-OO')-cobalt(ii)-di-iron(iii) acetonitrile solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 883708: Experimental Crystal Structure Determination

2013

Related Article: Julia R. Shakirova, Elena V. Grachova, Alexei S. Melnikov, Vladislav V. Gurzhiy, Sergey P. Tunik, Matti Haukka, Tapani A. Pakkanen, and Igor O. Koshevoy|2013|Organometallics|32|4061|doi:10.1021/om301100v

(mu~3~-tris(Diphenylphosphino)methane)-bis(mu~2~-eta^2^-3-hydroxy-33-diphenylprop-1-yn-1-yl)-bromo-(3-hydroxy-33-diphenylprop-1-yn-1-yl)-copper-tri-gold acetone solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 955946: Experimental Crystal Structure Determination

2013

Related Article: Julia R. Shakirova, Elena V. Grachova, Alexei S. Melnikov, Vladislav V. Gurzhiy, Sergey P. Tunik, Matti Haukka, Tapani A. Pakkanen, and Igor O. Koshevoy|2013|Organometallics|32|4061|doi:10.1021/om301100v

(mu~3~-tris(Diphenylphosphino)methane)-bis(mu~2~-eta^2^-3-hydroxy-33-diphenylprop-1-yn-1-yl)-chloro-(3-hydroxy-33-diphenylprop-1-yn-1-yl)-copper-tri-gold acetone solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1919440: Experimental Crystal Structure Determination

2019

Related Article: Jana Anhäuser, Rakesh Puttreddy, Lukas Glanz, Andreas Schneider, Marianne Engeser, Kari Rissanen, Arne Lützen|2019|Chem.-Eur.J.|25|12294|doi:10.1002/chem.201903164

ΔΔΔ)-hexakis(mu-(RP)-NN'-[tricyclo[8.2.2.247]hexadeca-1(12)46101315-hexaene-512-diylbis(41-phenylene)]bis[1-(pyridin-2-yl)methanimine])-tetra-iron(ii) octakis(trifluoromethanesulfonate) acetonitrile unknown solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Montanacin-L and montanacin-K two previously non-described acetogenins from Annona montana twigs and leaves

2020

A phytochemical study on Annona montana twigs and leaves led to the isolation of eleven annonaceous acetogenins, including two previously non-described compounds, montanacin-L and montanacin-K. Their structures were elucidated by extensive analyses of spectroscopic data (IR, UV, HRTOFMS, EI-MS and 1H, 13C and 2D NMR). The ACGs montanacin-L, montanacin-K, montanacin-D and montanacin-E were evaluated for their toxicity against Spodoptera frugiperda Smith (Lepidoptera: Noctuidae). Results revealed that montanacin-D and montanacin-K exhibited insecticide action. Fil: Ruiz Hidalgo, José. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán; …

010405 organic chemistryCiencias QuímicasPlant ScienceBiologybiology.organism_classification01 natural sciencesBiochemistryAnnona montana0104 chemical sciences010404 medicinal & biomolecular chemistryANNONACEOUS ACETOGENINSQuímica OrgánicaBotanyMONTANACIN-KAnnonaceous AcetogeninsINSECTICIDE ACTIONAgronomy and Crop ScienceMONTANACIN-LCIENCIAS NATURALES Y EXACTASBiotechnology
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Light Induced C-C Coupling of 2-Chlorobenzazoles with Carbamates, Alcohols, and Ethers.

2016

A light induced, transition-metal-free C-C coupling reaction of 2-chlorobenzazoles with aliphatic carbamates, alcohols, and ethers is presented. Inexpensive reagents, namely sodium acetate, benzophenone, water, and acetonitrile, are employed in a simple reaction protocol using a cheap and widely available 25 W energy saving UV-A lamp at ambient temperature.

010405 organic chemistryOrganic Chemistry010402 general chemistry01 natural sciencesCoupling reaction0104 chemical scienceschemistry.chemical_compoundC c couplingchemistryReagentLight inducedBenzophenoneOrganic chemistryAcetonitrileSodium acetateThe Journal of organic chemistry
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Essential Oil Yield, Chemical Composition, and Total Citral Content of Nine Cultivars of Cymbopogon Species from Western India

2016

ABSTRACTThe essential oil composition of five elite Cymbopogon varieties (OD-19, Pragati, RRL-16, NLG-84) and a hybrid (CPK-25) and four new selections (LS-1 to LS-4) were determined by gas chromatography (GC) and gas chromatography-mass spectrometry (GC-MS). The oil yield ranged from 0.31% to 1.0% with CPK-25 (1.0%) and LS-2 (0.95%) containing the highest. A total of 66 compounds, constituting 84.6–94.3% of the oils, were identified. The main compounds were geranial (29.9–41.6%), neral (25.8–32.5%), citronellol (0.3–12.8%), geranyl acetate (1.2–8.4%), and geraniol (1.8–8.2%). Of the cultivars, OD-19 (74.1%) had the highest and LS-3 (55.7%) contained the lowest amount of total citral. CKP-2…

0106 biological sciences0301 basic medicinePharmacologyCitronellolGeranyl acetateCitral01 natural scienceslaw.invention03 medical and health scienceschemistry.chemical_compoundHorticulture030104 developmental biologyComplementary and alternative medicinechemistrylawBotanyComposition (visual arts)CultivarGas chromatographyEssential oilGeraniol010606 plant biology & botanyJournal of Herbs, Spices & Medicinal Plants
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Chromatographic profiles and antimicrobial activity of the essential oils obtained from some species and cultivars of the Mentheae tribe (Lamiaceae)

2021

Abstract The present study was focused on the chemical composition and antimicrobial activity of the essential oils (EsO) obtained from five Lamiaceae representatives grown in the south of Ukraine. Among them are Salvia sclarea L., Monarda didyma (cultivar ‘Cambridge Scarlet’), Thymus pulegioides (cultivar ‘2/6-07’), Thymus vulgaris (cultivar ‘Jalos’), and Thymus serpyllum L. The component analysis of the EsO was carried out by gas chromatography method coupled with mass spectrometry (GC–MS). The antimicrobial properties of the EsO were determined using the agar diffusion test against widespread pathogenic bacterial strains (Staphylococcus aureus, Escherichia coli, Enterococcus faecalis, St…

0106 biological sciences0301 basic medicineQH301-705.5Monarda didymaThymus vulgarisThymus pulegioidesSalvia sclareaLinalyl acetate01 natural sciencesEssential oil03 medical and health scienceschemistry.chemical_compoundLinaloolSalvia sclareaGC–MSFood scienceBiology (General)Thymolbiologybiology.organism_classificationAntimicrobial030104 developmental biologyAntimicrobial effectchemistryThymus genusOriginal ArticleCultivarLamiaceaeGeneral Agricultural and Biological Sciences010606 plant biology & botanySaudi Journal of Biological Sciences
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