Search results for "Moiety"

showing 10 items of 621 documents

Ferrocenyl-Labeled Sugar Amino Acids: Conformation and Properties

2012

Novel organometallic sugar amino acid conjugates 1–5 have been prepared by amide coupling of O-protected N-acetylmuramic acid and iso-muramic acid (2-[3-amino-2, 5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxypropanoic acid) with 1-aminoferrocene, 1-aminoferrocene-1′-carboxylic acid (H-Fca-OH), or 1, 1′-diaminoferrocene, respectively. The influence of the ferrocenyl moiety and presence of additional remote potential hydrogen atom acceptors and donors at the ferrocenyl core on the conformation and lipophilicity is investigated by TLC, IR, NMR, and CD spectroscopic methods augmented by density functional calculations. Furthermore, the redox potential of the ferrocene/ferrocenium couple is tuned by…

chemistry.chemical_classificationHydrogen bondOrganic ChemistryMedicinal chemistryRedoxAmino acidInorganic Chemistrychemistry.chemical_compoundFerrocenechemistryconformational analysis; hydrogen bonds; metallocenes; redox chemistry; sugar amino acidsAmideLipophilicityOrganic chemistryMoietyHydroxymethylPhysical and Theoretical Chemistry
researchProduct

Der Phenylacetyl-(PhAc-)Rest als enzymatisch ablösbare Schutzgruppe für Peptide und Kohlenhydrate: Selektive Schutzgruppenabspaltungen mit Penicillin…

1988

N-Phenylacetyl-(PhAc-)-aminosauren werden mit Aminosauremethyl-, -benzyl-, -allyl- und -tert-butylestern mit Hilfe des modifizierten Carbodiimidverfahrens oder unter Verwendung von EEDQ in guten Ausbeuten zu vollgeschutzten Dipeptiden verknupft. Der PhAc-Rest ist bei den Abspaltungen der C-terminalen Schutzgruppen stabil, kann jedoch aus den Peptiden unter nahezu neutralen Bedingungen selektiv mit Penicillin-Acylase (EC 3.5.1.11) abgelost werden. Das Enzym hydrolysiert den PhAc-Rest auch aus der 2-Position von acetylgeschutzter Glucose, der 3-Position von Di-O-isopropylidenglucose und der primaren OH-Gruppe von Di-O-isopropyliden-L-sorbose. Bei den enzymatischen Abspaltungsreaktionen bleibe…

chemistry.chemical_classificationHydrolysischemistry.chemical_compoundPenicillin AcylaseEnzymechemistryStereochemistryOrganic ChemistryMoietyPhysical and Theoretical ChemistryCoupling reagentAmino acidCarbodiimideLiebigs Annalen der Chemie
researchProduct

Nonsteroidal Antiinflammatory Agents, XVIII: C-5 Functionalized 6,7-Diphenyl-2,3-dihydro-1H-pyrrolizines as Inhibitors of Bovine Cyclooxygenase and 5…

1994

6-(4-Chlorophenyl)-7-phenyl-2,3-dihydro-1H-pyrrolizines with functional groups at position 5 of the heterocyclic moiety were synthesized and tested. To determine their antiinflammatory activity bovine blood was used as enzyme source for the cyclooxygenase and 5-lipoxygenase, respectively. The iminoxy acetic acid derivative and the iminotetrazole selectively inhibit the 5-lipoxygenase, all the other compounds show medium or low affinity to the active sites of cyclooxygenase and 5-lipoxygenase. In general all compounds inhibit 5-lipoxygenase more effectively than cyclooxygenase. Concerning the inhibition of 5-lipoxygenase the most active compounds found are equipotent to the corresponding pro…

chemistry.chemical_classificationHydroxamic acidbiologyBicyclic moleculeStereochemistryAnti-Inflammatory Agents Non-SteroidalPharmaceutical ScienceStructure-Activity Relationshipchemistry.chemical_compoundEnzymeModels ChemicalchemistryEnzyme inhibitorDrug DiscoveryArachidonate 5-lipoxygenasebiology.proteinAnimalsStructure–activity relationshipMoietyCattleCyclooxygenase InhibitorsPyrrolesLipoxygenase InhibitorsCyclooxygenaseArchiv der Pharmazie
researchProduct

An Efficient and Simple Entry to N-Substituted beta-Enamino Acid Derivatives from 2-Alkyl-2-oxazolines and 2-Alkyl-2-thiazolines.

1996

Reaction of azaenolates of 2-alkyl-oxa(thia)zolines 6 with imidoyl chlorides 7 as electrophiles to furnish masked N-substituted beta-enamino acid derivatives 1-2 in 70-90% yield is described. Alternative routes are discussed. Compounds 1-2 generally appear in one tautomeric form, imino or enamino, depending on the nature of the imidoyl chloride. The configuration of the enamino moiety (Z) and the conformation (s-cis) of compounds 1-2 obtained were established by an NMR study and unequivocally set by nuclear Overhauser effect difference experiments. An X-ray structure of compound 1e is also reported, showing a strong intramolecular NH.N hydrogen bond. Ab initio calculations (HF/3-21G and HF/…

chemistry.chemical_classificationImidoyl chlorideHydrogen bondStereochemistryOrganic ChemistryNuclear Overhauser effectMedicinal chemistryTautomerchemistry.chemical_compoundchemistryIntramolecular forceElectrophileMoietyAlkylThe Journal of organic chemistry
researchProduct

Protonation, coordination chemistry, cyanometallate "supercomplex" formation and fluorescence chemosensing properties of a bis(2,2'-bipyridino)cyclop…

2013

A new polyazamacrocycle (L) containing two 2,2'-bipyridino (bpy) units, where the heteroaromatic nitrogen atoms point outwards from the macrocyclic cavity, was synthesized and characterized by elemental analysis, ESI-MS, (1)H and (13)C NMR, FTIR and TGA. Five protonation constants involving aliphatic nitrogens with log K in the range 9.39-3.07 were determined by potentiometry and NMR and a sixth protonation (log K = 2.2) involving a bipyridine moiety could be detected by UV-Vis and NMR titrations. The interaction of L with the cyanometallate anions [Pt(CN)4](2-) and [Co(CN)6](3-) was studied by potentiometry yielding respectively log K values in the ranges 4.0-6.4 and 5.2-10.5, covering pro…

chemistry.chemical_classificationInorganic chemistryProtonationBridging ligandCarbon-13 NMRCoordination complexInorganic ChemistryBipyridinechemistry.chemical_compoundCrystallographychemistryMoietyTitrationCyclophaneDalton transactions (Cambridge, England : 2003)
researchProduct

A Polar18F-Labeled Amino Acid Derivative for Click Labeling of Biomolecules

2014

This work describes the synthesis and 18F-labeling of an amino acid based prosthetic group that is able to participate in copper(I)-catalyzed cycloadditions. The prosthetic group can be used for 18F labeling of biomolecules under mild conditions. The synthesis started with L-serine methyl ester, which was derivatized by introducing an alkyne moiety and a leaving group for 18F labeling. Subsequently, 18F labeling as well as deprotection conditions were screened, which resulted in an overall radiochemical yield (RCY) of around 28 %. Furthermore, the 18F-labeled prosthetic group was treated with an azido cyclic Arg-Gly-Asp (cRGD) peptide as a model system in very high RCY of 98 %.

chemistry.chemical_classificationIsotopic labelingChemistryStereochemistryBiomoleculeOrganic ChemistryLeaving groupClick chemistryAlkyneMoietyPeptidePhysical and Theoretical ChemistryAmino acidEuropean Journal of Organic Chemistry
researchProduct

Light induced charging of polymer functionalized nanorods.

2010

ZnO nanorods were functionalized with new block copolymers containing a hole transporting moiety in one block and a dye and an anchor system in the second block. After functionalization, the ZnO nanorods are well dispersible in organic media and the fluorescence of the dye is quenched. Kelvin probe force microscopy was used to measure changes in electrical potential between the ZnO nanorod and the polymeric corona. Upon light irradiation, potential changes on the order of some tens of millivolts were observed on individual structures. This effect is attributed to light-induced charge separation between the ZnO nanorod and its hole transporting polymeric corona.

chemistry.chemical_classificationKelvin probe force microscopeMaterials scienceMechanical EngineeringBioengineeringNanotechnologyGeneral ChemistryPolymerCondensed Matter PhysicsFluorescencechemistryChemical engineeringMicroscopyCopolymerMoietySurface modificationGeneral Materials ScienceNanorodNano letters
researchProduct

Synthesis and pharmacological evaluation of enantiomerically pure endo-configured KOR agonists with 2-azabicyclo[3.2.1]octane scaffold

2021

Conformationally restricted bicyclic KOR agonists 10 with an endo configured amino moiety were synthesized to analyze the bioactive conformation of conformationally flexible KOR agonists such as 2-5. A seven-step, chiral pool synthesis starting with (S)-configured 4-oxopiperidine-2-carboxylate 13 was developed. cis and trans configured diesters 12 were obtained in a 3:1 ratio via hydrogenation of the α,β unsaturated ester 14. After establishment of the bicyclic scaffold, a diastereoselective reductive amination of ketone 11 provided exclusively the endo configured bicyclic amines 10a,b. The 3:1 mixtures of enantiomers were separated by chiral HPLC, respectively, leading to enantiomerically …

chemistry.chemical_classificationKetoneBicyclic moleculeStereochemistryOrganic ChemistryKOR agonistopioid receptorBiochemistryReductive aminationPyrrolidineChiral column chromatographychemistry.chemical_compoundchemistryChiral pool synthesis2-azabicyclo[3.2.1]octaneMoietyPhysical and Theoretical ChemistryEnantiomer
researchProduct

ChemInform Abstract: Synthesis of Functionalized Indoles with an α-Stereogenic Ketone Moiety Through an Enantioselective Friedel-Crafts Alkylation wi…

2010

Chiral complexes of BINOL-based ligands with hafnium tert-butoxide catalyze the enantioselective Friedel-Crafts alkylation of indoles with (E)-1,4-diaryl-2-butene-1,4-diones at room temperature, with good yields and ee up to 94%. Hafnium(IV) was found to be a more effective Lewis acid than other frequently used metal ions such as titanium(IV) or zirconium(IV). Unlike the enantioselective Friedel-Crafts alkylation of indoles with α,β-unsaturated compounds where the stereogenic center is generated in the β-position to a carbonyl group, the Friedel-Crafts alkylation with 2-butene-1,4-diones described here generates an α-stereogenic center with respect to one of the carbonyl groups. This can be…

chemistry.chemical_classificationKetoneChemistryEnantioselective synthesisMoietyGeneral MedicineLewis acids and basesAlkylationMedicinal chemistryFriedel–Crafts reactionStereocenterUmpolungChemInform
researchProduct

A unified synthetic approach to trachylobane-, beyerane-, atisane- and kaurane-type diterpenes

2006

A general synthetic approach to the polycyclic carbon skeleton of biogenetically related trachylobane, beyerane, atisane, and kaurane diterpenes from carvone is described. The skeleton of these diterpenes is prepared from a common intermediate, that is, 25, readily prepared from carvone using an IMDA reaction and an intramolecular diazo ketone cyclopropanation of an unsaturated ketone as key steps. The tetracyclic diterpene ring systems are obtained from this key trachylobane-type intermediate through the regioselective reductive cleavage of the cyclopropane ring, after adequate modification of the functionalization around the tricyclo[3.2.1.02,7]octane moiety.

chemistry.chemical_classificationKetoneCyclopropanationStereochemistryOrganic ChemistryRegioselectivityRing (chemistry)BiochemistryCyclopropanechemistry.chemical_compoundchemistryDrug DiscoveryOrganic chemistryMoietyDiazoDiterpeneTetrahedron
researchProduct