Search results for "DISCOVERY"

showing 10 items of 4119 documents

Reaction of an open-chain analogue of Reissert compound hydrofluoroborate salt with ethyl acrylate. A reinvestigation

1998

Abstract The reaction of an open-chain analogue of Reissert compound hydrofluoroborate salt with ethyl acrylate does not give a [4+2] cycloadduct as previously described, but a [3+2] cycloadduct which evolves to a 2-pyridone 15.

chemistry.chemical_classification10120 Department of Chemistry1303 Biochemistry3002 Drug DiscoveryOrganic ChemistrySalt (chemistry)BiochemistryMedicinal chemistrychemistry.chemical_compoundchemistryChain (algebraic topology)Drug Discovery540 ChemistryEthyl acrylateOrganic chemistry1605 Organic Chemistry
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Two New Triterpene Saponins from Cyclamen africanumBoiss. & Reuter

2012

Two new oleanane-type triterpene saponins, afrocyclamins A and B (1 and 2, resp.), were isolated from a MeOH extract of the roots of Cyclamen africanum Boiss. & Reuter, together with three known triterpenoid saponins, lysikokianoside, deglucocyclamin I, and its dicrotalic acid derivative. The structures were elucidated, on the basis of 1D- and 2D-NMR experiments and mass spectrometry as (3β,20β)-13,28-epoxy-16-oxo-3-{O-β-D-xylopyranosyl-(12)-O-β-D-glucopyranosyl-(14)-O-[β-D-glucopyranosyl-(12)]-α-L-arabinopyranosyl}oxy}oleanan-29-al (1) and (3β,16α,20β)-16,28,29-trihydroxy-olean-12-en-3-yl O-4-O-(4-carboxy-3-hydroxy-3-methyl-1-oxobutyl)-β-D-xylopyranosyl-(12)-O-β-D-glucopyranosyl-(14)-O-[β-…

chemistry.chemical_classificationAcid derivativebiologyChemistryStereochemistryOrganic Chemistrybiology.organism_classificationMass spectrometryBiochemistryCatalysisInorganic ChemistryTerpeneCyclamen africanumTriterpenoidTriterpeneDrug DiscoveryPhysical and Theoretical ChemistryHelvetica Chimica Acta
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A novel phosphorus–carbon bond formation by ring opening with diethyl phosphite of oxazolines derived from serine

2004

Abstract A new reaction of oxazolines derived from serine with diethyl phosphite leading to ring opening products with P–C bond formation is reported. This reaction, which proceeds under neutral conditions and without the use of any halogenated intermediate, results in a mixture of racemic α- and β-phosphono alanines in an approximate 1:2 ratio, with isolated yields up to 77%. The mechanism involves the rearrangement of the oxazoline into the corresponding α-benzamido acrylate, followed by addition of the diethyl phosphite to the double bond. Since no significant transesterification is observed, this method constitutes a simple route for α- and β-phosphono amino acids bearing suitable prote…

chemistry.chemical_classificationAcrylateDouble bondOrganic Chemistrychemistry.chemical_elementOxazolineTransesterificationRing (chemistry)BiochemistryMedicinal chemistryAmino acidSerinechemistry.chemical_compoundchemistryDrug DiscoveryOrganic chemistryCarbonTetrahedron
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Biodegradable microtablets made of low molecular weight polyglycolic acid: Bioabbaubare Mikrotabletten aus niedermolekularer Polyglycolsäure

1991

Research work in developing pharmaceutical dosage forms with biodegradable polymers seldom dealt with polyglycolic acid (PGA)1,2. This because of difficult processing procedures and low solubility of PGA in common organic solvents2,3. The only licensed product of the homoplymer in medical use is the sufgical suture Dexon®4

chemistry.chemical_classificationActive ingredientPharmaceutical technologyPolymer scienceChemistryStereochemistryDrug DiscoveryPharmaceutical SciencePolymerBiodegradationBiodegradable polymerDosage formArchiv der Pharmazie
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Unsaturated carboxylic acid dienolates. Addition to substituted cyclohexanones. Inverted kinetic and thermodynamic stereoselectivities.

1987

Abstract Addition of the lithium dienolate derived from crotonic acid to monosubstituted cyclohexanones occurs through the α and γ carbon atoms of the dienolate in the cold and on heating, respectively. For any regioselectivity, equatorial approach is found under kinetic conditions, but equilibration favours products from axial attack and selectivity may be inverted.

chemistry.chemical_classificationAddition reactionKetoneCarboxylic acidOrganic Chemistrychemistry.chemical_elementRegioselectivityBiochemistryMedicinal chemistrychemistryDrug DiscoveryOrganic chemistryLithiumStereoselectivityAliphatic compoundSelectivityTetrahedron Letters
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Trienediolates of hexadienoic acids in synthesis. synthesis of retinoic and nor-retinoic acids.

1993

Abstract Double deprotonation of either (E,E)-3-methyl-2,4-hexadienoic acid 2, or 4,6-dimethyldihydro-2-pyrone 3 generates apparently the same lithium trienediolate, which affords ω-hydroxy acids 9 on reaction with ketones 7. Hydroxy acids 9 are easily dehydrated to octatrienoic acids 5, which are structurally related to retinoic acid. Similarly, sorbic acid 1 leads to nor-retinoic acid analogs 6.

chemistry.chemical_classificationAddition reactionKetoneChemistryOrganic ChemistryRetinoic acidBiochemistrychemistry.chemical_compoundDeprotonationDrug DiscoveryOrganic chemistryStereoselectivityAliphatic compoundSorbic acidAcetophenoneTetrahedron
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A synthetic hexapeptide (Argireline) with antiwrinkle activity

2008

Botulinum neurotoxins (BoNTs) represent a revolution in cosmetic science because of their remarkable and long-lasting antiwrinkle activity. However, their high neurotoxicity seriously limits their use. Thus, there is a need to design and validate non-toxic molecules that mimic the action of BoNTs. The hexapeptide Ac-EEMQRR-NH2 (coined Argireline) was identified as a result of a rational design programme. Noteworthy, skin topography analysis of an oil/water (O/W) emulsion containing 10% of the hexapeptide on healthy women volunteers reduced wrinkle depth up to 30% upon 30 days treatment. Analysis of the mechanism of action showed that Argireline significantly inhibited neurotransmitter relea…

chemistry.chemical_classificationAgingRational designNeurotoxicityPharmaceutical SciencePeptideDermatologymedicine.diseaseExocytosisColloid and Surface ChemistryMechanism of actionchemistryBiochemistryChemistry (miscellaneous)In vivoDrug DiscoveryToxicitymedicineNeurotoxinmedicine.symptomInternational Journal of Cosmetic Science
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Enantioselective addition of Et2Zn to seven‐membered cyclic imines catalyzed by a (R)-VAPOL-Zn(II) complex

2017

Various substituted dibenzo[b,f][1,4]oxazepines underwent an enantioselective alkylation with Et2Zn catalyzed by a (R)-VAPOL-Zn(II) complex. The corresponding chiral 11-ethyl-10,11-dihydrodibenzo[b,f][1,4]oxazepine derivatives were obtained with good yields and moderate enantioselectivities. This represents the first example of enantioselective addition of Et2Zn to cyclic aldimines.

chemistry.chemical_classificationAldimine010405 organic chemistryChemistryStereochemistryOrganic ChemistryEnantioselective synthesischemistry.chemical_elementZincAlkylation010402 general chemistry01 natural sciencesBiochemistry0104 chemical sciencesCatalysischemistry.chemical_compoundCatàlisiDrug DiscoveryOxazepineQuímica orgànicaTetrahedron Letters
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Enantioselective addition of terminal alkynes to N-(diphenylphosphinoyl)imines catalyzed by Zn–BINOL complexes

2012

Abstract Chiral nonracemic N-(diphenylphosphinoyl)-protected propargylic amines have been prepared by addition of terminal alkynes to N-(diphenylphosphinoyl)aldimines in the presence of dimethylzinc and 3,3′-dibromo-BINOL as catalyst. The reaction works with a variety of aromatic and heteroaromatic aldimines and with different alkynes, providing the expected products in generally good yields and enantiomeric excesses (up to 96%).

chemistry.chemical_classificationAldiminechemistry.chemical_compoundchemistryOrganic ChemistryDrug DiscoveryDimethylzincEnantioselective synthesisEnantiomerBiochemistryMedicinal chemistryCatalysisTetrahedron
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Facile synthesis of 2-nitroalkanols by tetramethylguanidine (TMG)-catalyzed addition of primary nitroalkanes to aldehydes and alicyclic ketones

1997

Abstract Tetramethylguanidine-catalyzed addition of primary nitroalkanes to aldehydes and alicyclic ketones constitutes a practical means to perform the nitro-aldol reaction (Henry reaction). The very mild conditions employed, together with the short reaction times, make the procedure tolerant of a range of functionalities and highly versatile for the synthesis of a variety of 2-nitroalkanols.

chemistry.chemical_classificationAlicyclic compoundPrimary (chemistry)Nitroaldol reactionChemistryOrganic ChemistryDrug DiscoveryOrganic chemistryBiochemistryCatalysisTetrahedron Letters
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