Search results for "synthesis"

showing 10 items of 2844 documents

Manganese carbonyl terpyridyl complexes: their synthesis, characterization and potential application as CO-release molecules

2014

MnI carbonyl terpyridyl complexes have been synthesized and characterized. The tricarbonyl derivative exhibits interesting behaviors for controlled CO-release by both thermal and photosynthetic pathways.

Carbon MonoxideManganeseLightMetals and Alloyschemistry.chemical_elementGeneral ChemistryManganesePhotosynthesisPhotochemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCharacterization (materials science)chemistry.chemical_compoundchemistryCoordination ComplexesMaterials ChemistryCeramics and CompositesMolecule[CHIM]Chemical SciencesCo releaseta116Derivative (chemistry)ComputingMilieux_MISCELLANEOUSChemical Communications
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Comparative biochemistry of CO2 fixation and the evolution of autotrophy

1999

Carbon dioxide fixation is a polyphyletic trait that has evolved in widely separated prokaryotic branches. The three principal CO2-assimilation pathways are (i) the reductive pentose-phosphate cycle, i. e. the Calvin-Benson cycle; (ii) the reductive citric acid (or Arnon) cycle; and (iii) the net synthesis of acetyl-CoA from CO/CO2, or Wood pathway. Sequence analysis and the comparative biochemistry of these routes suggest that all of them were shaped to a considerable extent by the evolutionary recruitment of enzymes. Molecular phylogenetic trees show that the Calvin-Benson cycle was a relatively late development in the (eu)bacterial branch, suggesting that some form(s) of carbon assimilat…

Carbon dioxide assimilationArnon cycleCalvin-Benson cycle; Arnon cycle; Wood pathway; Semi-enzymatic synthesis; Carbon dioxide assimilationCalvin-Benson cycle:CIENCIAS DE LA VIDA::Microbiología [UNESCO]Wood pathwaySemi-enzymatic synthesisUNESCO::CIENCIAS DE LA VIDA::Microbiología
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Carbon autonomy of peach shoots determined by 13C-photoassimilate transport

2009

We used (13)CO(2) tracing and source-sink manipulation to determine if fruiting shoots of peach (Prunus persica (L.) Batsch) trees are autonomous or if they import carbon from neighboring shoots, and if the degree of shoot autonomy is influenced by the source-sink relationship of the shoot. In three experiments, leaf to fruit ratio (L:F) of selected fruiting shoots was moderately (2005 and 2006) or strongly (complete sink removal, 2006) altered to either enhance or inhibit movement of carbon from (13)C-labeled fruiting shoots (LFS) to adjacent non-labeled shoots (NLFS), both located within 10 cm on the same main scaffold of V-shaped peach trees. At Stages I and III of fruit growth, fruit an…

Carbon metabolismPhysiologyPlant ScienceBiologyPhotosynthesisSink (geography)Prunuschemistry.chemical_compoundBotanyCultivarPhotosynthesisCarbon Isotopesgeographygeography.geographical_feature_categoryBiological TransportCarbon DioxideCarbonPlant LeavesHorticulturePhotoassimilatechemistryFruitShootCarbon dioxidebranch girdling carbon dioxide fruit sink leaf area isotope tracing Prunus persica source-sink balancePrunusPlant ShootsTree Physiology
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Procollagen C-Proteinase Enhancer 1 (PCPE-1) is a marker of myocardial fibrosis and impaired cardiac function in a murine model of pressure overload

2021

Abstract(1)AimsProcollagen C-proteinase enhancer 1 (PCPE-1) is an extracellular matrix protein and a major regulator of fibrillar collagen biosynthesis. Previous work has shown that its abundance is often increased in the context of tissue repair and fibrosis. The present study was designed to evaluate its potential as a biomarker of myocardial interstitial fibrosis (MIF), a well-established pathogenic pathway leading to heart failure.(2)Methods and ResultsCardiac fibrosis was induced in rats using an optimized model of chronic pressure overload triggered by angiotensin II and Nω-nitro-L-arginine methyl ester (L-NAME). All treated animals suffered from heart hypertrophy and the increase in …

Cardiac function curvemedicine.medical_specialtyCardiac fibrosis[SDV]Life Sciences [q-bio]Diastoleheart failure030204 cardiovascular system & hematology03 medical and health sciences0302 clinical medicineFibrosisInternal medicinemedicine030304 developmental biologyPressure overload0303 health sciencesCardiac fibrosiscirculating biomarkerbusiness.industrycollagen biosynthesismedicine.diseaseProcollagen C-proteinase enhancer 1 (PCPE-1)Angiotensin IIEndocrinologyHeart failureMyocardial fibrosisPET-MR imagingbusiness
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Friedel-Crafts Alkylation of Arenes in Total Synthesis

2015

Cascade reactionChemistryTotal synthesisOrganic chemistryFriedel–Crafts reaction
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Synthesis and activity of phosphinic tripeptide inhibitors of cathepsin C

2004

Phosphinic tripeptide analogues Gly-Xaaψ[P(O)(OH)CH2]-Gly have been developed as inhibitors of cathepsin C (DPP I), a lysosomal, papain-like cysteine protease. The target compounds were synthesised by addition of methyl acrylate to the appropriate phosphinic acids followed by the N-terminus elongation using mixed anhydride procedure. The latter step has been demonstrated to be a suitable method for N-terminal extension of the phosphinic pseudopeptide analogues without requirement of hydroxyphosphinyl protection. The title compounds appeared to be moderate inhibitors of the cathepsin C. However, although designed as transition state analogues, they surprisingly exhibited noncompetitive mode …

Cathepsinchemistry.chemical_classificationnoncompetitive inhibitionStereochemistryphosphinic tripeptidesOrganic ChemistryClinical BiochemistryPharmaceutical ScienceBiological activityPeptideTripeptidePhosphinic AcidsBiochemistryCysteine proteaseChemical synthesisCathepsin CCathepsin CNon-competitive inhibitionchemistryDrug DiscoveryMolecular MedicineProtease InhibitorsOligopeptidesMolecular BiologyBioorganic & Medicinal Chemistry Letters
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Squaramide-Catalyzed Enantioselective Michael Addition of Pyrazol-3- ones to ortho-Quinone Methides

2020

A bifunctional squaramide catalyzed the enantioselective Michael addition of pyrazol-3- ones to ortho-quinone methides, generated in situ from 2-(1-tosylalkyl)phenols is presented. The corresponding chiral pyrazolones are obtained with good to excellent yields (27-98%) and enantiomeric excess (14-99% ee).

CatàlisiChemistryOrganic ChemistryMichael reactionEnantioselective synthesisSquaramideBiochemistryMedicinal chemistryQuímica orgànicaQuinoneCatalysis
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Organocatalytic Enantioselective Aminoalkylation of 5‐Aminopyrazole Derivatives with Cyclic Imines

2020

The first enantioselective alkylation of 5‐aminopyrazoles is described with good results. The organocatalytic alkylation of 5‐aminopyrazoles have been accomplished using benzoxathiazine 2,2‐dioxides as electrophiles and a bifunctional squaramide organocatalyst.

CatàlisiChemistryOrganocatalysisOrganic ChemistryEnantioselective synthesisPhysical and Theoretical ChemistryQuímica orgànicaCombinatorial chemistryEuropean Journal of Organic Chemistry
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Asymmetric Oxidative Mannich Reactions

2020

The asymmetric Mannich reaction is one of the most straightforward methodologies for the enantioselective synthesis of chiral amines. In general, asymmetric Mannich reactions involve the use of imines as electrophiles. However, in recent years, several asymmetric oxidative Mannich reactions have been reported using amines as electrophiles. This review provides an overview of these recent publications, including the different oxidants used and the scope and limitations of the different catalytic systems.

CatàlisiChemistryReacció d'oxidació-reduccióEnantioselective synthesisOrganic chemistryGeneral ChemistryOxidative phosphorylationAminesMannich reaction
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Enantioselective Synthesis of Functionalized Diazaspirocycles from 4‐Benzylideneisoxazol‐5(4H)‐one Derivatives and Isocyanoacetate Esters

2020

Enantioenriched spirocyclic compounds bearing three contiguous stereocenters and high functionalization were obtained through a formal [3+2] cycloaddition reaction catalyzed by a cooperative system. The spiro compounds were synthesized from 4-arylideneisoxazol-5-ones and isocyanoacetate esters using a bifunctional squaramide/Brønsted base organocatalyst derived from a Cinchona alkaloid and silver oxide as Lewis acid. This method afforded two out of the four possible diastereomers with good yields and high enantiomeric excess for both diastereomers.

CatàlisiCompostos orgànicsChemistryEnantioselective synthesisGeneral ChemistryQuímica orgànicaCombinatorial chemistryCycloadditionAdvanced Synthesis & Catalysis
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