Search results for "ALDEHYDE"

showing 10 items of 915 documents

Mitochondrial aldehyde dehydrogenase (ALDH-2)--maker of and marker for nitrate tolerance in response to nitroglycerin treatment.

2008

The hemodynamic and anti-ischemic effects of nitroglycerin (GTN) are rapidly blunted as a result of the development of nitrate tolerance. Long-term nitrate treatment also is associated with decreased vascular responsiveness caused by changes in intrinsic mechanisms of the tolerant vasculature itself. According to the oxidative stress concept, increased vascular superoxide and peroxynitrite production as well as an increased sensitivity to vasoconstrictors secondary to activation of protein kinase C as well as vascular NADPH oxidases contribute to the development of tolerance. Recent experimental work has defined new tolerance mechanisms, including inhibition of the enzyme that bioactivates …

Aldehyde dehydrogenasePharmacologyToxicologymedicine.disease_causeProstacyclin synthasechemistry.chemical_compoundNitroglycerinDrug tolerancemedicineHumansEndothelial dysfunctionchemistry.chemical_classificationReactive oxygen speciesNitratesbiologyAldehyde Dehydrogenase MitochondrialGeneral MedicineDrug ToleranceAldehyde Dehydrogenasemedicine.diseaseMitochondriaOxidative StresschemistryBiochemistrycardiovascular systembiology.proteinSoluble guanylyl cyclasePeroxynitriteOxidative stresscirculatory and respiratory physiologyChemico-biological interactions
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Catalytic Diastereo- and Enantioselective Synthesis of Tertiary Trifluoromethyl Carbinols through a Vinylogous Aldol Reaction of Alkylidenepyrazolone…

2022

A diastereo- and enantioselective organocatalytic aldol reaction between alkylidenepyrazolones and trifluoromethyl ketones leading to chiral tertiary alcohols bearing a trifluoromethyl group is presented. The methodology is based on the use of a bifunctional organocatalyst in order to activate the γ-hydrogen atoms of the alkylidenepyrazolone nucleophile and the carbonyl group of the trifluoromethylarylketone providing highly functionalized trifluoromethyl alcohols with moderate yields, excellent diastereoselectivity, and moderate to good enantioselectivity. Experiments monitoring the conversion by 1H NMR and the enantiomeric excess by HPLC with the reaction time showed that full conversion …

AldehydesCatàlisiMethanolOrganic ChemistryStereoisomerismKetonesQuímica orgànica
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New Insight to the Chemistry of Polyaza[n]paracyclophanes. A 15N NMR Study

2001

AldehydesMagnetic Resonance SpectroscopyNitrogen IsotopesChemistryOrganic ChemistryTitrimetryHydrogen-Ion ConcentrationEthers CyclicMetalsCationsAlkanesPolyaminesOrganic chemistryChemistry (relationship)The Journal of Organic Chemistry
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One-pot synthesis of polysubstituted indolizines by an addition/cycloaromatization sequence.

2013

Indolizines carrying various substituents in positions 5-8 were obtained from readily available 2-(1H-pyrrol-1-yl)nitriles and α,β-unsaturated ketones or aldehydes in a one-pot procedure. Michael addition of the deprotonated aminonitriles to the acceptors followed by acid-catalyzed electrophilic cyclization produces 5,6-dihydroindolizine-5-carbonitriles. From these stable intermediates, substituted indolizines were obtained via base-induced dehydrocyanation.

AldehydesMolecular StructureStereochemistryChemistryOrganic ChemistryOne-pot synthesisIndolizinesSequence (biology)KetonesDeprotonationCyclizationElectrophileNitrilesMichael reactionMoleculeThe Journal of organic chemistry
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Stereoselective anti aldol reactions of erythrulose derivatives. Functionalized chiral d3 and d4 synthons.

2004

An improved procedure for the synthesis of anti aldols from protected erythrulose derivatives is reported. The preparation of functionalized d3 and d4 synthons with various stereochemical arrays by means of this methodology is described and subsequently applied to a stereoselective formal synthesis of the natural metabolite goniothalesdiol.

AldehydesMolecular StructureStereochemistryMetaboliteOrganic ChemistrySynthonStereoisomerismErythruloseStereoisomerismKetonesChemical synthesischemistry.chemical_compoundLactoneschemistryAldol reactionStereoselectivityAldol condensationTetrosesThe Journal of organic chemistry
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Bis(oxazoline) Lewis Acid Catalyzed Aldol Reactions of PyridineN-Oxide Aldehydes—Synthesis of Optically Active 2-(1-Hydroxyalkyl)pyridine Derivatives…

2006

A new, short, and simplified procedure for the synthesis of optically active pyridine derivatives from pro-chiral pyridine-N-oxides is presented. The catalytic and asymmetric Mukaiyama aldol reaction between ketene silyl acetals and 1-oxypyridine-2-carbaldehyde derivatives catalyzed by chiral copper(II)-bis(oxazoline) complexes gave optically active 2-(hydroxyalkyl)- and 2-(anti-1,2-dihydroxyalkyl)pyridine derivatives in good yields and diastereoselectivities, and in excellent enantioselectivities-up to 99 % enantiomeric excess. As a synthetic application of the developed method, a full account for the asymmetric total synthesis of a nonnatural indolizine alkaloid is provided.

AldehydesOptics and PhotonicsPyridinesChemistryOrganic ChemistryIndolizinesEnantioselective synthesisTotal synthesisPyridine-N-oxideStereoisomerismGeneral ChemistryOxazolineCatalysisCyclic N-OxidesChemistrychemistry.chemical_compoundAlkaloidsAldol reactionPyridineOrganic chemistryIndolizineEnantiomeric excessAcidsChemistry - A European Journal
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Synthesis of terpenoid unsaturated 1,4-dialdehydes. Pi-facial selectivity in the Diels-Alder reaction of the 1-vinyl-2-methylcyclohexene moiety of po…

2000

AldehydesVinyl CompoundsMolecular StructureChemistryAcetyleneTerpenesOrganic ChemistryMolecular ConformationTerpenoidAlkynesMoietyOrganic chemistryIndicators and ReagentsSelectivityDiels–Alder reactionThe Journal of organic chemistry
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Disinfectants in Dialysis: Dangers, Drawbacks and Disinformation

1988

Aldehydesmedicine.medical_specialtybusiness.industrySurgeryDisinfectionIodophorsRenal DialysisAlcoholsDisinformationmedicineHumansPeracetic AcidChlorineDialysis (biochemistry)Intensive care medicinebusinessPeritoneal DialysisDisinfectantsNephron
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Reaction products and pathways in the selective oxidation of C-2-C-4 alkanes on MoVTeNb mixed oxide catalysts

2010

[EN] The catalytic properties of MoVTeNbO catalysts during the selective oxidation of short chain alkanes and olefins (C-2-C-4) have been comparatively studied The main reaction products have been ethylene from ethane acrylic acid from propane maim anhydride from n-butane and methacrolein from isobutane FTIR studies of the adsorption of the main reaction products i e olefins and aldehydes over MoVTeNbO catalyst has been carried out Accordingly the reaction pathway is explained on the basis of the characteristics of the alkane fed the stability and reactivity of both the intermediates and the reaction products and the nature of the catalytic sites involved in each reaction (C) 2010 Elsevier …

Alkanechemistry.chemical_classificationMaleic anhydrideButaneMethacroleinGeneral ChemistryAldehydeCatalysisCatalysisMoVTeNb mixed oxideschemistry.chemical_compoundchemistryIsobutaneOrganic chemistryReactivity (chemistry)Selective oxidation of alkanesIn situ FTIR spectra
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Investigation of the aqueous transmetalation of π-allylpalladium with indium salt: the use of the Pd(OAc)2–TPPTS catalyst

2005

pi-Allylpalladium complexes could be generated in water by the palladium(0) water soluble catalyst prepared in situ from palladium acetate and TPPTS. These complexes were transmetalated with indium to react with benzaldehyde. The aqueous solution of Pd(0)(TPPTS)(n) could be reused without deterioration of the catalyst in the first and second recycling. The system proved to be efficient with primary and secondary allylic substrates. The stereochemical outcome of the allylation through umpolung of allylpalladium, was also studied using models with a restraint conformation.

Allylic rearrangementInorganic chemistrychemistry.chemical_elementBiochemistryUmpolungCatalysisBenzaldehydeTransmetalationchemistry.chemical_compoundBARBIER-TYPE ALLYLATIONSORGANOMETALLIC REACTIONSPolymer chemistryWATERPhysical and Theoretical ChemistryTPPTSSIALIC-ACIDAqueous solutionIN-SITUOrganic ChemistryMEDIATED ALLYLATIONCARBONYL-COMPOUNDSALCOHOLSREGIOSELECTIVITYORGANIC-SYNTHESISSettore CHIM/06 - Chimica OrganicachemistryPalladiumOrg. Biomol. Chem.
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