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Referências encontradas : 124 [refinar]
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[PMID]:28407955
[Au] Autor:Lago LO; Nicolli KP; Marques AB; Zini CA; Welke JE
[Ad] Endereço:Instituto de Ciência e Tecnologia de Alimentos, Universidade Federal do Rio Grande do Sul, Avenida Bento Gonçalves 9500, CEP: 91501-970 Porto Alegre, RS, Brazil.
[Ti] Título:Influence of ripeness and maceration of the grapes on levels of furan and carbonyl compounds in wine - Simultaneous quantitative determination and assessment of the exposure risk to these compounds.
[So] Source:Food Chem;230:594-603, 2017 Sep 01.
[Is] ISSN:0308-8146
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:The validated method based on the use of headspace solid phase microextraction (HS-SPME) coupled with the comprehensive two-dimensional gas chromatography with time-of-flight mass spectrometric detection (GC×GC/TOFMS) proved to be appropriate for this first simultaneous quantitative determination of six toxic compounds (formaldehyde, acetaldehyde, ethyl carbamate, furan, furfural and acrolein) found in wines. Acetaldehyde and acrolein coeluted with other wine compounds, which indicated that difficulties could arise if only one-dimensional gas chromatography was used for the determination of these compounds. The advancement of the ripeness degree and increasing the grape maceration time seems to result in higher concentrations of toxic compounds. The exposure to furan, acrolein and ethyl carbamate through wine consumption may pose risks to consumer health, since calculated MOE values were lower than 10,000.
[Mh] Termos MeSH primário: Cromatografia Gasosa/métodos
Furanos/química
Compostos Carbonílicos de Ferro/química
Vitis/química
Vinho/análise
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Furans); 13463-40-6 (Iron Carbonyl Compounds); UC0XV6A8N9 (furan)
[Em] Mês de entrada:1705
[Cu] Atualização por classe:170512
[Lr] Data última revisão:
170512
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170415
[St] Status:MEDLINE


  2 / 124 MEDLINE  
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[PMID]:26233567
[Au] Autor:Li M; Yang D; Brock G; Knipp RJ; Bousamra M; Nantz MH; Fu XA
[Ad] Endereço:Department of Chemical Engineering, University of Louisville, Louisville, KY 40292, United States.
[Ti] Título:Breath carbonyl compounds as biomarkers of lung cancer.
[So] Source:Lung Cancer;90(1):92-7, 2015 Oct.
[Is] ISSN:1872-8332
[Cp] País de publicação:Ireland
[La] Idioma:eng
[Ab] Resumo:OBJECTIVE: Lung cancer dysregulations impart oxidative stress which results in important metabolic products in the form of volatile organic compounds (VOCs) in exhaled breath. The objective of this work is to use statistical classification models to determine specific carbonyl VOCs in exhaled breath as biomarkers for detection of lung cancer. MATERIALS AND METHODS: Exhaled breath samples from 85 patients with untreated lung cancer, 34 patients with benign pulmonary nodules and 85 healthy controls were collected. Carbonyl compounds in exhaled breath were captured by silicon microreactors and analyzed by Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR-MS). The concentrations of carbonyl compounds were analyzed using a variety of statistical classification models to determine which compounds best differentiated between the patient sub-populations. Predictive accuracy of each of the models was assessed on a separate test data set. RESULTS: Six carbonyl compounds (C(4)H(8)O, C(5)H(10)O, C(2)H(4)O(2), C(4)H(8)O(2), C(6)H(10)O(2), C(9)H(16)O(2)) had significantly elevated concentrations in lung cancer patients vs. CONTROLS: A model based on counting the number of elevated compounds out of these six achieved an overall classification accuracy on the test data of 97% (95% CI 92%-100%), 95% (95% CI 88%-100%), and 89% (95% CI 79%-99%) for classifying lung cancer patients vs. non-smokers, current smokers, and patients with benign nodules, respectively. These results were comparable to benchmarking based on established statistical and machine-learning methods. The sensitivity in each case was 96% or higher, with specificity ranging from 64% for benign nodule patients to 86% for smokers and 100% for non-smokers. CONCLUSION: A model based on elevated levels of the six carbonyl VOCs effectively discriminates lung cancer patients from healthy controls as well as patients with benign pulmonary nodules.
[Mh] Termos MeSH primário: Biomarcadores Tumorais/metabolismo
Compostos Carbonílicos de Ferro/metabolismo
Neoplasias Pulmonares/metabolismo
Compostos Orgânicos Voláteis/metabolismo
[Mh] Termos MeSH secundário: Adulto
Idoso
Biomarcadores Tumorais/análise
Testes Respiratórios/métodos
Estudos de Casos e Controles
Expiração/fisiologia
Feminino
Seres Humanos
Compostos Carbonílicos de Ferro/análise
Neoplasias Pulmonares/classificação
Neoplasias Pulmonares/patologia
Masculino
Meia-Idade
Nódulos Pulmonares Múltiplos/classificação
Nódulos Pulmonares Múltiplos/metabolismo
Nódulos Pulmonares Múltiplos/patologia
Valor Preditivo dos Testes
Sensibilidade e Especificidade
Fumar/metabolismo
Espectroscopia de Infravermelho com Transformada de Fourier/métodos
Compostos Orgânicos Voláteis/análise
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Nome de substância:
0 (Biomarkers, Tumor); 0 (Volatile Organic Compounds); 13463-40-6 (Iron Carbonyl Compounds)
[Em] Mês de entrada:1606
[Cu] Atualização por classe:150908
[Lr] Data última revisão:
150908
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:150803
[St] Status:MEDLINE


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[PMID]:24746831
[Au] Autor:Tang Y; Li Y; Yu H; Gao C; Liu L; Chen S; Xing M; Liu L; Yao P
[Ad] Endereço:Department of Nutrition and Food Hygiene, Hubei Key Laboratory of Food Nutrition and Safety, Ministry of Education Key Laboratory of Environment and Health and MOE Key Lab of Environment and Health, Key Laboratory of Environment and Health (Wuhan), Ministry of Environmental Protection, State Key Lab
[Ti] Título:Quercetin prevents ethanol-induced iron overload by regulating hepcidin through the BMP6/SMAD4 signaling pathway.
[So] Source:J Nutr Biochem;25(6):675-82, 2014 Jun.
[Is] ISSN:1873-4847
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Emerging evidence has demonstrated that chronic ethanol exposure induces iron overload, enhancing ethanol-mediated liver damage. The purpose of this study was to explore the effects of the naturally occurring compound quercetin on ethanol-induced iron overload and liver damage, focusing on the signaling pathway of the iron regulatory hormone hepcidin. Adult male C57BL/6J mice were pair-fed with isocaloric-Lieber De Carli diets containing ethanol (accounting for 30% of total calories) and/or carbonyl iron (0.2%) and treated with quecertin (100 mg/kg body weight) for 15 weeks. Mouse primary hepatocytes were incubated with ethanol (100 mM) and quercetin (100 µM) for 24 h. Mice exposed to either ethanol or iron presented significant fatty infiltration and iron deposition in the liver; these symptoms were exacerbated in mice cotreated with ethanol and iron. Quercetin attenuated the abnormity induced by ethanol and/or iron. Ethanol suppressed BMP6 and intranuclear SMAD4 as well as decreased hepcidin expression. These effects were partially alleviated by quercetin supplementation in mice and hepatocytes. Importantly, ethanol caused suppression of SMAD4 binding to the HAMP promoter and of hepcidin messenger RNA expression. These effects were exacerbated by anti-BMP6 antibody and partially alleviated by quercetin or human recombinant BMP6 in cultured hepatocytes. In contrast, co-treatment with iron and ethanol, especially exposure of iron alone, activated BMP6/SMAD4 pathway and up-regulated hepcidin expression, which was also normalized by quercetin in vivo. Quercetin prevented ethanol-induced hepatic iron overload different from what carbonyl iron diet elicited in the mechanism, by regulating hepcidin expression via the BMP6/SMAD4 signaling pathway.
[Mh] Termos MeSH primário: Antioxidantes/uso terapêutico
Suplementos Nutricionais
Modelos Animais de Doenças
Insuficiência Hepática/prevenção & controle
Sobrecarga de Ferro/prevenção & controle
Fígado/metabolismo
Quercetina/uso terapêutico
[Mh] Termos MeSH secundário: Animais
Antioxidantes/metabolismo
Proteína Morfogenética Óssea 6/agonistas
Proteína Morfogenética Óssea 6/antagonistas & inibidores
Proteína Morfogenética Óssea 6/genética
Proteína Morfogenética Óssea 6/metabolismo
Células Cultivadas
Etanol
Regulação da Expressão Gênica
Insuficiência Hepática/etiologia
Hepatócitos/metabolismo
Hepcidinas/agonistas
Hepcidinas/antagonistas & inibidores
Hepcidinas/genética
Hepcidinas/metabolismo
Seres Humanos
Compostos Carbonílicos de Ferro
Sobrecarga de Ferro/metabolismo
Sobrecarga de Ferro/patologia
Sobrecarga de Ferro/fisiopatologia
Fígado/patologia
Masculino
Camundongos Endogâmicos C57BL
Quercetina/metabolismo
Distribuição Aleatória
Proteínas Recombinantes/metabolismo
Transdução de Sinais
Proteína Smad4/agonistas
Proteína Smad4/antagonistas & inibidores
Proteína Smad4/genética
Proteína Smad4/metabolismo
[Pt] Tipo de publicação:COMPARATIVE STUDY; JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Nome de substância:
0 (Antioxidants); 0 (Bone Morphogenetic Protein 6); 0 (Hepcidins); 0 (Recombinant Proteins); 0 (Smad4 Protein); 0 (Smad4 protein, mouse); 13463-40-6 (Iron Carbonyl Compounds); 3K9958V90M (Ethanol); 9IKM0I5T1E (Quercetin)
[Em] Mês de entrada:1412
[Cu] Atualização por classe:140512
[Lr] Data última revisão:
140512
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:140422
[St] Status:MEDLINE


  4 / 124 MEDLINE  
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[PMID]:24458644
[Au] Autor:Kuchenreuther JM; Myers WK; Suess DL; Stich TA; Pelmenschikov V; Shiigi SA; Cramer SP; Swartz JR; Britt RD; George SJ
[Ad] Endereço:Department of Chemistry, University of California, Davis, Davis, CA 95616, USA.
[Ti] Título:The HydG enzyme generates an Fe(CO)2(CN) synthon in assembly of the FeFe hydrogenase H-cluster.
[So] Source:Science;343(6169):424-7, 2014 Jan 24.
[Is] ISSN:1095-9203
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Three iron-sulfur proteins--HydE, HydF, and HydG--play a key role in the synthesis of the [2Fe](H) component of the catalytic H-cluster of FeFe hydrogenase. The radical S-adenosyl-L-methionine enzyme HydG lyses free tyrosine to produce p-cresol and the CO and CN(-) ligands of the [2Fe](H) cluster. Here, we applied stopped-flow Fourier transform infrared and electron-nuclear double resonance spectroscopies to probe the formation of HydG-bound Fe-containing species bearing CO and CN(-) ligands with spectroscopic signatures that evolve on the 1- to 1000-second time scale. Through study of the (13)C, (15)N, and (57)Fe isotopologs of these intermediates and products, we identify the final HydG-bound species as an organometallic Fe(CO)2(CN) synthon that is ultimately transferred to apohydrogenase to form the [2Fe](H) component of the H-cluster.
[Mh] Termos MeSH primário: Proteínas de Bactérias/química
Domínio Catalítico
Hidrogenase/química
Compostos Carbonílicos de Ferro/metabolismo
Proteínas com Ferro-Enxofre/química
[Mh] Termos MeSH secundário: Catálise
Shewanella putrefaciens/enzimologia
Espectroscopia de Infravermelho com Transformada de Fourier
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, N.I.H., EXTRAMURAL; RESEARCH SUPPORT, NON-U.S. GOV'T; RESEARCH SUPPORT, U.S. GOV'T, NON-P.H.S.
[Nm] Nome de substância:
0 (Bacterial Proteins); 0 (Iron-Sulfur Proteins); 13463-40-6 (Iron Carbonyl Compounds); EC 1.12.- (iron hydrogenase); EC 1.12.7.2 (Hydrogenase)
[Em] Mês de entrada:1402
[Cu] Atualização por classe:161019
[Lr] Data última revisão:
161019
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:140125
[St] Status:MEDLINE
[do] DOI:10.1126/science.1246572


  5 / 124 MEDLINE  
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[PMID]:24458630
[Au] Autor:Pickett CJ
[Ad] Endereço:Energy Materials Laboratory, School of Chemistry, University of East Anglia, Norwich NR4 7 TJ, UK.
[Ti] Título:Biochemistry. Making the H-cluster from scratch.
[So] Source:Science;343(6169):378-9, 2014 Jan 24.
[Is] ISSN:1095-9203
[Cp] País de publicação:United States
[La] Idioma:eng
[Mh] Termos MeSH primário: Proteínas de Bactérias/química
Domínio Catalítico
Hidrogenase/química
Compostos Carbonílicos de Ferro/metabolismo
Proteínas com Ferro-Enxofre/química
[Pt] Tipo de publicação:COMMENT; JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Bacterial Proteins); 0 (Iron-Sulfur Proteins); 13463-40-6 (Iron Carbonyl Compounds); EC 1.12.- (iron hydrogenase); EC 1.12.7.2 (Hydrogenase)
[Em] Mês de entrada:1402
[Cu] Atualização por classe:140124
[Lr] Data última revisão:
140124
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:140125
[St] Status:MEDLINE
[do] DOI:10.1126/science.1249276


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[PMID]:24287103
[Au] Autor:Gonzales MA; Mascharak PK
[Ad] Endereço:Department of Chemistry and Biochemistry, University of California, Santa Cruz, CA 95064.
[Ti] Título:Photoactive metal carbonyl complexes as potential agents for targeted CO delivery.
[So] Source:J Inorg Biochem;133:127-35, 2014 Apr.
[Is] ISSN:1873-3344
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:The surprising discovery of carbon monoxide (CO) as a signaling molecule in mammalian physiology has recently raised interest in this toxic gas among researchers in biochemical and pharmaceutical community. CO is endogenously produced mainly from catabolism of heme by the enzyme heme oxygenase (HO) and participates in a myriad of anti-inflammatory, anti-proliferative, and vasoregulatory pathways. In animal models, low doses of CO have exhibited beneficial effects in suppression of organ graft rejection and safeguarding the heart during reperfusion after cardiopulmonary bypass surgery. The salutary effects of CO have naturally drawn attention of the pharmaceutical industry for its use as a cytoprotective agent. Safety-related concerns of the use of this noxious gas have prompted research in the area of syntheses of CO-releasing molecules (CORMs) and to date, several metal carbonyls (metal complexes of CO) have been employed as CORMs in promoting prolonged (and safe) delivery of low doses of CO to cellular targets. Because many carbonyl complexes release CO upon illumination, investigators have recently began to explore the possibility of "controlled CO delivery" through the use of light. During the past few years, a number of photoactive CORMs or "photoCORMs" have been synthesized that release CO upon illumination with UV or visible light. The utility of these photoCORMs in CO delivery has also been confirmed. Novel design principles for isolation of photoCORMs have started to appear in recent reports. Scrutiny of the literature reveals the emergence of a new exciting area of drug development in such efforts. The potential of photoCORMs as CO-donating pharmaceuticals along with a brief overview of the physiological roles of CO is presented in this review.
[Mh] Termos MeSH primário: Monóxido de Carbono/metabolismo
Complexos de Coordenação/metabolismo
Transdução de Sinais/genética
[Mh] Termos MeSH secundário: Animais
Monóxido de Carbono/química
Complexos de Coordenação/química
Cristalografia por Raios X
Heme/metabolismo
Seres Humanos
Compostos Carbonílicos de Ferro/metabolismo
Metais/química
Metais/metabolismo
Modelos Moleculares
Vasodilatação/fisiologia
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, N.I.H., EXTRAMURAL; RESEARCH SUPPORT, U.S. GOV'T, NON-P.H.S.; REVIEW
[Nm] Nome de substância:
0 (Coordination Complexes); 0 (Metals); 13463-40-6 (Iron Carbonyl Compounds); 42VZT0U6YR (Heme); 7U1EE4V452 (Carbon Monoxide)
[Em] Mês de entrada:1411
[Cu] Atualização por classe:140317
[Lr] Data última revisão:
140317
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:131130
[St] Status:MEDLINE


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[PMID]:23863109
[Au] Autor:Blanco E; Lam S; Smoukov SK; Velikov KP; Khan SA; Velev OD
[Ad] Endereço:Department of Chemical & Biomolecular Engineering, North Carolina State University, Raleigh, North Carolina 27695, United States.
[Ti] Título:Stability and viscoelasticity of magneto-Pickering foams.
[So] Source:Langmuir;29(32):10019-27, 2013 Aug 13.
[Is] ISSN:1520-5827
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:We have developed a new class of bistable Pickering foams, which can remain intact for weeks at room temperature but can be destroyed rapidly and on-demand with the use of a magnetic field. Such responsive foam systems can find application in various industrial and environmental processes that require controlled defoaming. These foams are stabilized by particles of hypromellose phthalate (HP-55) and contain oleic acid-coated carbonyl iron particles embedded in the HP-55 matrix. The complex behavior of these foams arises from several factors: a robust anisotropic particle matrix, the capacity to retain a high amount of water, as well as an age-dependent response to an external field. We report how the structure and viscoelastic properties of the foams change with time and affect their collapse characteristics. The evolution of foam properties is quantified by measuring the rate of liquid drainage from the foam as well as the rate of bubble growth in the foam with respect to time elapsed (in the absence of a magnetic field). We also evaluate the time necessary for foam collapse in magnetic fields as a function of magnetic particle content. A decreasing liquid volume fraction in the foam during aging leads to an increase in the elasticity and rigidity of the foam structure. These data allow us to identify a transition time separating two distinct stages of foam development in the absence of field. We propose different mechanisms which control foam collapse for each stage in a magnetic field. The stiffening of foam films between air bubbles with age plays a key role in distinguishing between the two destabilization regimes.
[Mh] Termos MeSH primário: Compostos Carbonílicos de Ferro/química
Metilcelulose/análogos & derivados
Ácidos Oleicos/química
[Mh] Termos MeSH secundário: Campos Magnéticos
Metilcelulose/química
Tamanho da Partícula
Propriedades de Superfície
Viscosidade
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T; RESEARCH SUPPORT, U.S. GOV'T, NON-P.H.S.
[Nm] Nome de substância:
0 (Oleic Acids); 13463-40-6 (Iron Carbonyl Compounds); 9004-67-5 (Methylcellulose); 9050-31-1 (hydroxypropyl methylcellulose phthalate)
[Em] Mês de entrada:1402
[Cu] Atualização por classe:130813
[Lr] Data última revisão:
130813
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:130719
[St] Status:MEDLINE
[do] DOI:10.1021/la4014224


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[PMID]:23165638
[Au] Autor:Braunschweig H; Radacki K; Shang R; Tate CW
[Ad] Endereço:Institut für Anorganische Chemie, Julius-Maximilians-Universität Würzburg, Germany. h.braunschweig@uni-wuerzburg.de
[Ti] Título:Reversible intramolecular coupling of the terminal borylene and a carbonyl ligand of [Cp(CO)2Mn=B-tBu].
[So] Source:Angew Chem Int Ed Engl;52(2):729-33, 2013 Jan 07.
[Is] ISSN:1521-3773
[Cp] País de publicação:Germany
[La] Idioma:eng
[Ab] Resumo:Cyclic complex 2 with bridging carbonyl ligands was synthesized from a facile and reversible intermolecular carbonyl-borylene ligand coupling reaction at room temperature. Complex 2 exhibits an unprecedented coordination mode for boron-metal complexes, which is also reflected in its remarkable (11)B NMR chemical shift of -57.2 ppm. Findings from spectroscopic, X-ray, and computational studies are presented, along with a proposed mechanism.
[Mh] Termos MeSH primário: Complexos de Coordenação/química
Compostos Carbonílicos de Ferro/química
Manganês/química
[Mh] Termos MeSH secundário: Compostos de Boro/química
Ligantes
Modelos Moleculares
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Nome de substância:
0 (Boron Compounds); 0 (Coordination Complexes); 0 (Ligands); 13463-40-6 (Iron Carbonyl Compounds); 42Z2K6ZL8P (Manganese)
[Em] Mês de entrada:1309
[Cu] Atualização por classe:131121
[Lr] Data última revisão:
131121
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:121121
[St] Status:MEDLINE
[do] DOI:10.1002/anie.201207017


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[PMID]:23106368
[Au] Autor:Leclercq IA
[Ti] Título:Pro-oxidants or anti-oxidant defenses? Which one to blame in non-alcoholic steatohepatitis pathogenesis?
[So] Source:J Gastroenterol Hepatol;27(11):1651-3, 2012 Nov.
[Is] ISSN:1440-1746
[Cp] País de publicação:Australia
[La] Idioma:eng
[Mh] Termos MeSH primário: Gorduras na Dieta/farmacologia
Expressão Gênica/efeitos dos fármacos
Compostos Carbonílicos de Ferro/farmacologia
Ferro/metabolismo
Fígado/metabolismo
Fator 2 Relacionado a NF-E2/genética
[Mh] Termos MeSH secundário: Animais
Masculino
[Pt] Tipo de publicação:COMMENT; EDITORIAL
[Nm] Nome de substância:
0 (Dietary Fats); 0 (NF-E2-Related Factor 2); 0 (Nfe2l2 protein, mouse); 13463-40-6 (Iron Carbonyl Compounds); E1UOL152H7 (Iron)
[Em] Mês de entrada:1305
[Cu] Atualização por classe:131121
[Lr] Data última revisão:
131121
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:121031
[St] Status:MEDLINE
[do] DOI:10.1111/j.1440-1746.2012.07255.x


  10 / 124 MEDLINE  
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[PMID]:23024977
[Au] Autor:Das S; Li Y; Junge K; Beller M
[Ad] Endereço:Leibniz-Insitut für Katalyse e.V., Albert-Einstein-Strasse 29a, 18059, Rostock, Germany.
[Ti] Título:Synthesis of ethers from esters via Fe-catalyzed hydrosilylation.
[So] Source:Chem Commun (Camb);48(87):10742-4, 2012 Nov 11.
[Is] ISSN:1364-548X
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:Triiron dodecacarbonyl allows for the selective reduction of esters into the corresponding ethers. This protocol has a wide substrate scope. In addition, cholesteryl pelarogonate has been reduced under the reaction conditions with an excellent yield.
[Mh] Termos MeSH primário: Ésteres/química
Éteres/síntese química
Compostos Carbonílicos de Ferro/química
Compostos de Organossilício/química
[Mh] Termos MeSH secundário: Catálise
Éteres/química
Estrutura Molecular
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Esters); 0 (Ethers); 0 (Organosilicon Compounds); 13463-40-6 (Iron Carbonyl Compounds)
[Em] Mês de entrada:1303
[Cu] Atualização por classe:121008
[Lr] Data última revisão:
121008
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:121002
[St] Status:MEDLINE
[do] DOI:10.1039/c2cc32142d



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