Search results for "hydroxylation"

showing 10 items of 102 documents

Direct Difluorination–Hydroxylation, Trifluorination, and C(sp2)–H Fluorination of Enamides

2018

A direct double functionalization involving both difluorination and hydroxylation of enamides is reported. With the appropriate combination of an electrophilic fluorinating reagent and H2O, the most convenient and ecofriendly hydroxylating agent, the preparation of 3-(difluoroalkyl)-3-hydroxyisoindolin-1-ones was achieved under basic or Bronsted acidic conditions. Suitable conditions for trifluorination as well as C(sp2)–H fluorination were also identified. Subsequent asymmetric functionalization of the obtained gem-difluorinated products has also been demonstrated.

010405 organic chemistryOrganic Chemistry010402 general chemistry01 natural sciencesBiochemistryCombinatorial chemistry0104 chemical sciencesHydroxylationchemistry.chemical_compoundchemistryReagentElectrophileSurface modificationPhysical and Theoretical ChemistryOrganic Letters
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Total Synthesis of (-)-Oxycodone via Anodic Aryl-Aryl Coupling.

2019

A fully regio- and diastereoselective electrochemical 4a–2′-coupling of a 3′,4′,5′-trioxygenated laudanosine derivative enables the synthesis of the corresponding morphinandienone. This key intermediate is further transformed into (−)-oxycodone through conjugate nucleophilic substitution for E-ring closure and [4 + 2] cycloaddition with photogenerated singlet oxygen to accomplish diastereoselective hydroxylation at C-14. The anodic transformation provides high yields and can be performed under constant current conditions both in a simple undivided cell or in continuous flow.

010405 organic chemistrySinglet oxygenArylOrganic ChemistryTotal synthesis010402 general chemistryElectrochemistry01 natural sciencesBiochemistryCombinatorial chemistryCycloaddition0104 chemical sciencesHydroxylationchemistry.chemical_compoundchemistryNucleophilic substitutionPhysical and Theoretical ChemistryConjugateOrganic letters
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’Structural constraints in cyanobacteria-mediated whole-cell biotransformation of methoxylated and methylated derivatives of 2′-hydroxychalcone

2019

Halophilic and freshwater strains of cyanobacteria representing the Oscillatoriales, Nostocales, Chroococcales, and Synechococcales orders of Cyanophyta were examined to determine (i) the resistance of their cultures when suppressed by the presence of exogenous methoxylated and methylated derivatives of 2'-hydroxychalcone, (ii) morphological changes in cells treated with the tested chalcones and, most importantly, (iii) whether these photoautotrophic microorganisms transform chalcone derivatives in a structure- or strain-dependent manner. The growth of cyanobacterial cultures depended on chalcone derivatives and the strain; nevertheless, trends for correlations between these parameters are …

0106 biological sciences0301 basic medicineCyanobacteriaChalconeStereochemistrySubstituentBioengineeringCyanobacteriaHydroxylation01 natural sciencesApplied Microbiology and BiotechnologyMethylationHydroxylation03 medical and health scienceschemistry.chemical_compoundChalconesBiotransformation010608 biotechnologyBiotransformationNostocalesSynechococcalesHydrogenative bioreductionbiologyEthoxylationGeneral Medicinebiology.organism_classification030104 developmental biologychemistryOscillatorialesWhole-cell biotransformationBiotechnologyJournal of Biotechnology
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Arginase induction represses gall development during clubroot infection in Arabidopsis.

2012

Arginase induction can play a defensive role through the reduction of arginine availability for phytophageous insects. Arginase activity is also induced during gall growth caused by Plasmodiophora brassicae infection in roots of Arabidopsis thaliana; however, its possible role in this context has been unclear. We report here that the mutation of the arginase-encoding gene ARGAH2 abrogates clubroot-induced arginase activity and results in enhanced gall size in infected roots, suggesting that arginase plays a defensive role. Induction of arginase activity in infected roots was impaired in the jar1 mutant, highlighting a link between the arginase response to clubroot and jasmonate signaling. C…

0106 biological sciencesClubrootArabidopsis thalianaPhysiologyPyridinesArabidopsisplantPlant SciencePlasmodiophorida01 natural sciencesPlant RootsCallogenesisPlant Epidermischemistry.chemical_compoundJasmonateArabidopsisPlant TumorsGallArabidopsis thalianaJasmonateAmino AcidsComputingMilieux_MISCELLANEOUSchemistry.chemical_classification0303 health sciencesJasmonic acidfood and beveragesGeneral MedicineCell biologyArginasePLANT SCIENCESOrgan SpecificityPlasmodiophora brassicaeEnzyme Inductionnitric-oxideCyclopentanesBiologyHydroxylationAmidohydrolasesClubroot03 medical and health sciencesAuxinBotanymedicinethalianaOxylipinsIsoleucine030304 developmental biologydiseaseArginaseArabidopsis Proteinsfungijasmonic acid[SDV.BBM.BM]Life Sciences [q-bio]/Biochemistry Molecular Biology/Molecular biologyplasmodiophora-brassicaeCell BiologyDiazonium Compoundsbiology.organism_classificationmedicine.diseaserootarginine catabolism[SDV.BV.AP]Life Sciences [q-bio]/Vegetal Biology/Plant breedingchemistryMutationidentificationaccumulation010606 plant biology & botanyPlantcell physiology
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Effect of the cytochrome P-450 inactivator 1-aminobenzotriazole on the metabolism of chlortoluron and isoproturon in wheat

1987

Abstract Roots of young wheat plants ( Triticum aestivum cv Clement) were treated with [ 14 C]chlortoluron or [ 14 C]isoproturon alone or mixed with 1-aminobenzotriazole (ABT), a mechanism-based inactivator of cytochrome P -450 monooxygenases. Radioactivity extracted from shoots slightly decreased during periods of metabolism, this decrease being reduced by ABT in the case of isoproturon. ABT strongly inhibited the metabolism of both herbicides. Accumulation of metabolites was generally depressed in the presence of ABT; however, levels of the free N -monodemethylated derivatives were little or not affected. It is concluded that ABT is a synergist of chlortoluron and isoproturon in wheat bec…

0106 biological sciencesCytochromeStereochemistry[SDV]Life Sciences [q-bio]Health Toxicology and Mutagenesis01 natural sciencesHydroxylationchemistry.chemical_compoundComputingMilieux_MISCELLANEOUSDemethylationchemistry.chemical_classificationbiologyChemistryfood and beveragesCytochrome P45004 agricultural and veterinary sciencesGeneral MedicineMetabolismMonooxygenase[SDV] Life Sciences [q-bio]EnzymeBiochemistryChlortoluron040103 agronomy & agriculturebiology.protein0401 agriculture forestry and fisheriesAgronomy and Crop Science010606 plant biology & botany
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Metabolism of chlortoluron in tolerant species: possible role of cytochrome p-450 mono-oxygenases

1988

Summary Pathways of chlortoluron metabolism were compared in excised leaves of four tolerant species, namely wheat (Triticum aestivum var Clement), Bromus sterilis, Galium aparine and Veronica persica. The herbicide was principally detoxified by hydroxylation of the ring methyl in wheat and by N-dealkylation in Veronica persica. Both pathways were involved in Bromus sterilis and Galium aparine. Kinetic study of the degradation showed that capacity to form non-toxic conjugates could, at least partially, explain the tolerance of these species to chlortoluron. In plants treated with 1-aminobenzotriazole, a cytochrome P-450 enzyme inactivator, N-dealkylation of chlortoluron was little or not af…

0106 biological sciencesCytochrome[SDV]Life Sciences [q-bio]Plant Science01 natural sciencesGaliumHydroxylation03 medical and health scienceschemistry.chemical_compoundBotanyMono oxygenaseComputingMilieux_MISCELLANEOUSEcology Evolution Behavior and Systematics030304 developmental biologyBromus sterilis0303 health sciencesbiologyMetabolismbiology.organism_classification[SDV] Life Sciences [q-bio]chemistryChlortoluronbiology.proteinAgronomy and Crop ScienceVeronica persica010606 plant biology & botany
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A Dehydrogenase Dual Hydrogen Abstraction Mechanism Promotes Estrogen Biosynthesis: Can We Expand the Functional Annotation of the Aromatase Enzyme?

2018

Cytochrome P450 (CYP450) enzymes are involved in the metabolism of exogenous compounds and in the synthesis of signaling molecules. Among the latter, human aromatase (HA) promotes estrogen biosynthesis, which is a key pharmacological target against breast cancers. After decades of debate, interest in gaining a comprehensive picture of HA catalysis has been renewed by the recent discovery that compound I (Cpd I) is the reactive species of the peculiar aromatization step. Herein, for the first time, a complete atomic-level picture of all controversial steps of estrogen biosynthesis is presented. By performing cumulative quantum-classical molecular dynamics and metadynamics simulations of abou…

0301 basic medicineCell signalingDehydrogenase-Molecular Dynamics Simulation010402 general chemistryHydroxylation01 natural sciencesenzyme catalysisCatalysisEnzyme catalysisHydroxylation03 medical and health scienceschemistry.chemical_compoundAromataseCytochrome P-450 Enzyme SystemHumansAromatasechemistry.chemical_classificationhydrogen abstractionbiologyOrganic ChemistryAromatizationAndrostenedioneCytochrome P450EstrogensGeneral Chemistrymolecular dynamics0104 chemical sciencesreaction mechanisms030104 developmental biologyEnzymechemistryBiochemistrySettore CHIM/03 - Chimica Generale E Inorganicadensity functional calculationsbiology.proteinProtonsOxidoreductasesOxidation-ReductionHydrogen
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Biocatalytic hydrogenation of the C=C bond in the enone unit of hydroxylated chalcones-process arising from cyanobacterial adaptations.

2018

To verify the hypothesis that cyanobacteria naturally biosynthesising polyphenolic compounds possess an active enzymatic system that enables them to transform these substances, such an ability of the biocatalytic systems of whole cells of these biota was assessed for the first time. One halophilic strain and seven freshwater strains of cyanobacteria representing four of the five taxonomic orders of Cyanophyta were examined to determine the following: (i) whether they contain polyphenols, including flavonoids; (ii) the resistance of their cultures when suppressed by the presence of exogenous hydroxychalcones—precursors of flavonoid biosynthesis and (iii) whether these photoautotrophs can tra…

0301 basic medicineCyanobacteriaStereochemistryHydroxylated chalconesCyanobacteria01 natural sciencesApplied Microbiology and BiotechnologyHydroxylation03 medical and health scienceschemistry.chemical_compoundChalconesbiology010405 organic chemistryfood and beveragesGeneral MedicineCarbon-13 NMRbiology.organism_classification0104 chemical sciencesRegiospecific hydrogenation030104 developmental biologyFlavonoid biosynthesisApplied Microbial and Cell PhysiologychemistryPolyphenolBiocatalysisProton NMRBiocatalysisHydrogenationEnoneBiotechnologyApplied microbiology and biotechnology
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Free energy profiles for two ubiquitous damaging agents: methylation and hydroxylation of guanine in B-DNA

2017

International audience; DNA methylation and hydroxylation are two ubiquitous reactions in DNA damage induction, yet insights are scarce concerning the free energy of activation within B-DNA. We resort to multiscale simulations to investigate the attack of a hydroxyl radical and of the primary diazonium onto a guanine embedded in a solvated dodecamer. Reaction free energy profiles characterize two strongly exergonic processes, yet allow unprecedented quantification of the barrier towards this damage reaction, not higher than 6 kcal mol−1 and sometimes inexistent, and of the exergonicities. In the case of the [G(C8)-OH]˙ intermediate, we challenge the functional dependence of such simulations…

0301 basic medicineGuanineGuanineDNA damageStereochemistryEntropyGeneral Physics and Astronomy010402 general chemistryHydroxylation01 natural sciencesHydroxylation03 medical and health scienceschemistry.chemical_compoundComputational chemistry[CHIM.ANAL]Chemical Sciences/Analytical chemistryPhysical and Theoretical ChemistryExergonic reactionchemistry.chemical_classificationHydroxyl RadicalBiomoleculeDNA Methylation0104 chemical sciences030104 developmental biologychemistryEnergy TransferDNA methylationHydroxyl radicalDNA B-Form[CHIM.RADIO]Chemical Sciences/RadiochemistryDNA
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Multigram Scale Enzymatic Synthesis of (R)-1-(4′-Hydroxyphenyl)ethanol Using Vanillyl Alcohol Oxidase

2018

The enantioselective oxyfunctionalisation of C−H bonds is a highly interesting reaction, as it provides access to chiral alcohols that are important pharmaceutical building blocks. However, it is hard to achieve using traditional methods. One way in which it can be achieved is through the action of oxidative enzymes. Although many reports of the oxyfunctionalisation capabilities of enzymes at an analytical scale have been published, reports on the use of enzymes to achieve oxyfunctionalisation on a synthetically relevant scale are fewer. Here, we describe the scale-up of the conversion of 4-ethylphenol to (R)-1-(4′-hydroxyphenyl)ethanol using the flavin-dependent enzyme vanillyl alcohol oxi…

0301 basic medicineVanillyl-alcohol oxidaseBiochemieEnantioselectivityHydroxylation01 natural sciencesBiochemistryHydroxylation03 medical and health scienceschemistry.chemical_compoundOxidative enzymeOrganic chemistryVLAGchemistry.chemical_classificationEthanol010405 organic chemistryChemistryEnantioselective synthesisSubstrate (chemistry)General ChemistryAlkylphenols0104 chemical sciencesFlavoprotein030104 developmental biologyEnzymeYield (chemistry)AlcoholsOxidoreductases
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