Search results for "cyclic"

showing 10 items of 2439 documents

Asymmetric synthesis of fluorinated amino macrolactones through ring-closing metathesis

2007

The synthesis of new chiral fluorinated amino and azamacrolactones of types 1 and 2 is described. A ring-closing metathesis (RCM) reaction constitutes the key step in this methodology, which uses fluorinated amino alcohols 7 as starting materials. The influence of the CF2 group, which is located in the alpha-position relative to the carbon bearing the amino group, on the efficiency of the RCM reaction is noteworthy. This method allows for the preparation of the desired fluorinated macrolactones in excellent yields.

chemistry.chemical_classificationModels MolecularMacrocyclic CompoundsHydrocarbons FluorinatedMolecular StructureOrganic ChemistryEnantioselective synthesisStereoisomerismStereoisomerismMetathesisCrystallography X-RayCombinatorial chemistryChemical synthesisAmino AlcoholsLactonesRing-closing metathesischemistryCyclizationMoleculeAmine gas treatingLactone
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Heterocyclic rearrangements in constrained media. A zeolite-directed photorearrangement of 1,2,4-oxadiazoles

2005

[reaction: see text] The first intrazeolite-photoinduced rearrangement of a five-membered heterocycle is reported. A completely different behavior compared to solution irradiations has been observed. The zeolite's role in directing the photoreaction of 3-phenyl-1,2,4-oxadiazoles toward the formation of the corresponding 1,3,4-oxadiazoles in a ring contraction-ringexpansion route is discussed.

chemistry.chemical_classificationModels MolecularOxadiazolesRING-PHOTOISOMERIZATIONMolecular StructurePHOTOCHEMICAL BEHAVIORChemistryPhotochemistryUltraviolet RaysOrganic ChemistryPATHWAYSSettore CHIM/06 - Chimica OrganicaRing (chemistry)PhotochemistryHeterocyclic compoundCyclizationZeolitesZeolite
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Cluster dirhenium(III) cis-dicarboxylates with α-amino acids ligands as mighty selective G4s binders.

2021

The synthesis of four dirhenium(III) cis-dicarboxylates with the α-amino acids residues Asp (I), Glu (II), Phe (III) and Tyr (IV) is presented. The G-quadruplex stabilization potential was evaluated by fluorescence resonance energy transfer - melting analysis. All derivatives show specific binding to c-kit1 quadruplex, while II and IV have also strong stabilization activity to HTelo21 quadruplex. At the same time, the compounds do not show any stabilization activity for ds26 DNA, which suggests unique mechanisms of molecular DNA recognition for these complexes.

chemistry.chemical_classificationMolecular StructureStereochemistrychemistry.chemical_elementDNARheniumG-quadruplexLigandsBiochemistryAmino acidInorganic ChemistryG-Quadruplexeschemistry.chemical_compoundFörster resonance energy transferRheniumchemistryCoordination ComplexesCluster (physics)Fluorescence Resonance Energy TransferHumansheterocyclic compoundsAmino AcidsDNADna recognitionJournal of inorganic biochemistry
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Reduction of benzo(a)pyrene mutagenicity by dihydrodiol dehydrogenase

1979

THE enigma of how inert chemicals can exert potent mutagenic, carcinogenic, allergenic and cytotoxic effects has been much debated. It has been learned that such compounds are metabolically converted to chemically reactive species1. In the case of aromatic or olefinic compounds, monooxygenases located in the membranes of the cell can transform these compounds into epoxides2–5 which by virtue of electrophilic reactivity can bind chemically to cellular macromolecules such as DNA, RNA and proteins, thereby disturbing biochemical control mechanisms and leading to the above mentioned toxic effects. The same membranes in which such epoxides are produced possess an enzyme, epoxide hydratase, which…

chemistry.chemical_classificationMultidisciplinarybiologyChemistryEpoxideMonooxygenaseCofactorAlcohol OxidoreductasesMiceStructure-Activity Relationshipchemistry.chemical_compoundEnzymeBiochemistryBenzo(a)pyreneMutationMicrosomes Liverpolycyclic compoundsbiology.proteinAnimalsPyreneBenzopyrenesBiotransformationCarcinogenDNANature
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Synthesis of novel isoxazoline-fused cispentacin stereoisomers

2009

Abstract New isoxazoline-fused cispentacins were prepared by the 1,3-dipolar cycloaddition of nitrile oxides to β-amino esters containing a cyclopentene skeleton. This synthetic procedure gave regio- and diastereoisomers of the cispentacins. The synthetic route was extended to the synthesis of these compounds in enantiomerically pure form.

chemistry.chemical_classificationNitrileBicyclic moleculeStereochemistryOrganic ChemistryDiastereomerCispentacinBiochemistryCycloadditionAmino acidchemistry.chemical_compoundchemistryDrug DiscoveryOrganic chemistryCyclopenteneTetrahedron Letters
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Selective nitrile oxide dipolar cycloaddition for the synthesis of highly functionalized β-aminocyclohexanecarboxylate stereoisomers

2012

Highly functionalized β-aminocyclohexanecarboxylate regio- and stereoisomers were synthesized from a bicyclic β-lactam by successive regioselective iodolactonization, stereo- and regioselective nitrile oxide cycloaddition, lactone ring-opening and isoxazoline ring-opening.

chemistry.chemical_classificationNitrileBicyclic moleculeStereochemistryOrganic ChemistryOxideIodolactonizationRegioselectivityBiochemistryCycloadditionchemistry.chemical_compoundchemistryDrug DiscoveryOrganic chemistryta116LactoneTetrahedron
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Stereoselective synthesis of carane-based chiral β- and γ-amino acid derivatives via conjugate addition

2015

Abstract Michael addition of dibenzylamine to (−)-tert-butyl isochaminate, prepared in three steps from (−)-perillaldehyde, furnished a carane-based β-amino acid derivative in a highly stereospecific reaction. The resulting amino ester was transformed to the bicyclic amino acid, a promising building block for the synthesis of 1,3-heterocycles and peptidomimetics. The conjugate addition of nitromethane to α,β-unsaturated methyl ester likewise resulted in nitro esters in stereospecific reactions. Catalytic reduction of the nitro group yielded a γ-amino ester. Under acidic conditions, the hydrolysis of the methyl ester resulted in an unexpected aminolactone-type product through rearrangement o…

chemistry.chemical_classificationNitromethaneBicyclic moleculeStereochemistryOrganic ChemistryEnantioselective synthesisBiochemistryAmino acidHydrolysischemistry.chemical_compoundStereospecificitychemistryDrug DiscoveryNitroMichael reactionamino acid derivativesta116stereoselective synthesiscaraneTetrahedron
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Diastereoselective synthesis of fluorinated, seven-membered beta-amino acid derivatives via ring-closing metathesis.

2003

[reaction: see text] Cis and trans seven-membered gamma,gamma-difluorinated beta-amino acid derivatives (III) have been prepared with a sequence that starts with imidoyl halides (I), which are condensed with suitable ester enolates to give intermediates (II). These, in turn, can be cyclized by means of a ring-closing olefin metathesis reaction and the product stereoselectively reduced to yield compounds (III) in good overall yields.

chemistry.chemical_classificationOlefin metathesisStereochemistryChemistryOrganic ChemistryHalideStereoisomerismGeneral MedicineFluorineBiochemistryMedicinal chemistryAmino acidTurn (biochemistry)Ring-closing metathesisYield (chemistry)Salt metathesis reactionPhysical and Theoretical ChemistryAmino AcidsBeta (finance)Cis–trans isomerismAcyclic diene metathesisOrganic letters
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Facile access to foldable redox-active flavin-peptide conjugates

2021

A convenient approach for the synthesis of foldable redox-active flavin peptide conjugates was established. A model β-hairpin oligopeptide motif was utilized to demonstrate that azidolysine side-chains are readily functionalised with an alkyne-bearing flavine derivative. The folding equilibrium of the peptide backbone as well as the redox behaviour of the flavin moieties remains intact after the conjugation.

chemistry.chemical_classificationOligopeptideChemistryOrganic ChemistryPeptideFlavin groupBiochemistryRedoxCombinatorial chemistryFolding (chemistry)chemistry.chemical_compoundRedox activeheterocyclic compoundsPhysical and Theoretical ChemistryPeptidesDerivative (chemistry)Conjugate
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Omphalotins E-I, Five Oxidatively Modified Nematicidal Cyclopeptides fromOmphalotus olearius

2009

Omphalotins E–I, oxidatively modified cyclic dodecapeptides, were isolated from mycelial extracts of the basidiomycete Omphalotus olearius, and their structures were determined by NMR spectroscopic and MS methods. Four of the five omphalotins contained an unprecedented N-hydroxylated tricyclic tryptophan derivative. All compounds exhibited strong and selective nematicidal activity against the plant pathogen Meloidogyne incognita with LD90 values between 2 and 5 μg mL–1. Cytotoxic activities were not detected up to 50 μg mL–1. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)

chemistry.chemical_classificationOmphalotus oleariusbiologyStereochemistryChemical structureOrganic ChemistryTryptophanBasidiomycotaNuclear magnetic resonance spectroscopybiology.organism_classificationCyclic peptidechemistryMeloidogyne incognitaOrganic chemistryPhysical and Theoretical ChemistryMyceliumEuropean Journal of Organic Chemistry
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