Search results for "Michael"

showing 10 items of 171 documents

Komedia tulevaisuuden Suomesta

2005

SuomiOakeshott Michaelkansallinen identiteettitulevaisuuskomediatstrategianarratologiaihmiskuva
researchProduct

Enantioselective Synthesis of Pyrrolizidinone Scaffolds through Multiple-Relay Catalysis

2020

A triple-tandem protocol for the synthesis of the pyrrolizidinone skeleton has been devised. It involves a cross metathesis-intramolecular aza-Michael reaction-intramolecular Michael addition tandem sequence, starting from N-pentenyl-4-oxo-2-alkenamides and conjugated ketones. In the presence of two cooperative catalysts, namely the second-generation Hoveyda-Grubbs catalyst and (R)-TRIP-derived BINOL phosphoric acid, this multiple-relay catalytic process takes place in good yields and outstanding levels of diastero- and enantioselectivity with the simultaneous generation of three contiguous stereocenters.

Tandem010405 organic chemistryOrganic ChemistryEnantioselective synthesisSequence (biology)Conjugated system010402 general chemistry01 natural sciencesBiochemistryCombinatorial chemistry0104 chemical sciencesCatalysisStereocenterchemistry.chemical_compoundchemistryMichael reactionPhysical and Theoretical ChemistryPhosphoric acidOrganic Letters
researchProduct

Microwave-assisted tandem cross metathesis intramolecular Aza-Michael reaction: an easy entry to cyclic beta-amino carbonyl derivatives.

2007

Hoveyda−Grubbs catalyst in combination with BF3·OEt2 efficiently promotes tandem cross metathesis intramolecular aza-Michael reaction between enones and unsaturated carbamates resulting in the creation of β-amino carbonyl units. The use of microwave irradiation dramatically accelerates the process, enhancing the synthetic utility of this methodology for the preparation of these types of derivatives. When enantiomerically enriched α-branched amines were used as starting materials, the process was also very efficient, although with modest selectivity in the newly created stereocenter. The use of microwave irradiation led to an interesting effect, inverting the selectivity in the addition proc…

TandemChemistryGeneral ChemistryMetathesisBiochemistryMicrowave assistedCatalysisCatalysisStereocenterColloid and Surface ChemistryIntramolecular forceMichael reactionOrganic chemistrySelectivityJournal of the American Chemical Society
researchProduct

ChemInform Abstract: Microwave-Assisted Tandem Cross Metathesis Intramolecular Aza-Michael Reaction: An Easy Entry to Cyclic β-Amino Carbonyl Derivat…

2008

Hoveyda−Grubbs catalyst in combination with BF3·OEt2 efficiently promotes tandem cross metathesis intramolecular aza-Michael reaction between enones and unsaturated carbamates resulting in the creation of β-amino carbonyl units. The use of microwave irradiation dramatically accelerates the process, enhancing the synthetic utility of this methodology for the preparation of these types of derivatives. When enantiomerically enriched α-branched amines were used as starting materials, the process was also very efficient, although with modest selectivity in the newly created stereocenter. The use of microwave irradiation led to an interesting effect, inverting the selectivity in the addition proc…

TandemChemistryIntramolecular forceSalt metathesis reactionMichael reactionGeneral MedicineSelectivityMetathesisCombinatorial chemistryCatalysisStereocenterChemInform
researchProduct

Synthetic and theoretical studies of novel ring closure and ring opening reactions

2006

Ring closure and ring opening reactions are in many cases useful synthetic procedures in organic chemistry. They allow the preparation of complex molecules with high stereoselectivity and good yields. Mechanistic and theoretical studies have been carried out on the transformation of 2-aminopyrimidines into imidazo[1,2-c]pyrimidines and guanidines, respectively, through ring closure and ring opening reactions, as well as the transamidation reactions through the ring closure and ring opening of guanidine derivatives, which constitute novel synthetic methods. Sepulveda Arques, Jose, Jose.Sepulveda@uv.es

Transamidation reactionUNESCO::QUÍMICAMichael addition:QUÍMICA::Química orgánica [UNESCO]Ring openingUNESCO::QUÍMICA::Química orgánicaImidazopyrimidines ; Guanidines ; Michael addition ; Ring closure ; Ring opening ; Transamidation reactionGuanidines:QUÍMICA [UNESCO]Ring closureImidazopyrimidines
researchProduct

Mg/BOX complexes as efficient catalysts for the enantioselective Michael addition of malonates to β-trifluoromethyl-α,β-unsaturated ketones and their…

2021

Abstract Magnesium (II)-BOX complexes catalyze the enantioselective Michael addition of malonates to β-trifluoromethyl enones and their N-sulfonyl imines to give ketones or (E)-enamines bearing a trifluoromethylated stereogenic center, respectively, with good yields and high enantiomeric excesses. Magnesium complexes proved to be more active and stereoselective than zinc and copper analogues in these reactions.

Trifluoromethyl010405 organic chemistryChemistryMagnesiumOrganic ChemistryEnantioselective synthesischemistry.chemical_elementZinc010402 general chemistry01 natural sciencesBiochemistryMedicinal chemistry0104 chemical sciencesStereocenterchemistry.chemical_compoundCatàlisiTosylDrug DiscoveryMichael reactionStereoselectivityQuímica orgànicaTetrahedron
researchProduct

Copper-catalysed enantioselective Michael addition of malonic esters to β-trifluoromethyl-α,β-unsaturated imines

2017

[EN] Copper triflate-BOX complexes catalyse the enantioselective conjugate addition of methyl malonate to beta-trifluoromethyl-alpha,beta-unsaturated imines to give the corresponding enamines bearing a trifluoromethylated stereogenic centre with good yields, and diastereo- and enantioselectivities. The usefulness of the method has been shown with the synthesis of optically active beta-trifluoromethyl delta-amino esters and optically active trifluoromethyl piperidones.

Trifluoromethyl010405 organic chemistryChemistryOrganic ChemistryEnantioselective synthesischemistry.chemical_elementOptically active010402 general chemistry01 natural sciencesBiochemistryCopper0104 chemical sciencesStereocenterchemistry.chemical_compoundCatàlisiMethyl malonateFISICA APLICADAMichael reactionOrganic chemistryPhysical and Theoretical ChemistryQuímica orgànicaConjugateOrganic & Biomolecular Chemistry
researchProduct

Development of Novel Benzodiazepine-Based Peptidomimetics as Inhibitors of Rhodesain from Trypanosoma brucei rhodesiense.

2020

Starting from the reversible rhodesain inhibitors 1 a-c, which have Ki values towards the target protease in the low-micromolar range, we have designed a series of peptidomimetics, 2 a-g, that contain a benzodiazepine scaffold as a β-turn mimetic; they are characterized by a specific peptide sequence for the inhibition of rhodesain. Considering that irreversible inhibition is strongly desirable in the case of a parasitic target, a vinyl ester moiety acting as Michael-acceptor was introduced as the warhead; this portion was functionalized in order to evaluate the size of corresponding enzyme pocket that could accommodate this substituent. With this investigation, we identified an irreversibl…

Trypanosoma brucei rhodesiensehuman African trypanosomiasiStereochemistryPeptidomimeticmedicine.medical_treatmentSubstituentAntiprotozoal AgentsTrypanosoma bruceiCysteine Proteinase Inhibitors01 natural sciencesBiochemistrychemistry.chemical_compoundBenzodiazepinesStructure-Activity RelationshipDrug DevelopmentParasitic Sensitivity TestsDrug DiscoverymedicineMoietyTrypanosoma bruceiGeneral Pharmacology Toxicology and PharmaceuticsPeptide sequencePharmacologyrhodesainProteasebiologyDose-Response Relationship DrugMolecular Structure010405 organic chemistryOrganic ChemistryTrypanosoma brucei rhodesiensebenzodiazepine scaffoldbiology.organism_classificationpeptidomimetic0104 chemical sciences010404 medicinal & biomolecular chemistryCysteine EndopeptidaseschemistryMolecular MedicinePeptidomimeticsMichael acceptorLead compoundChemMedChem
researchProduct

Double asymmetric intramolecular aza-Michael reaction: a convenient strategy for the synthesis of quinolizidine alkaloids.

2021

A new methodology to access the quinolizidine skeleton in an asymmetric fashion was devised. It involves two consecutive intramolecular aza-Michael reactions of sulfinyl amines bearing a bis-enone moiety, in turn generated by a monodirectional cross metathesis reaction. The sequence, which takes place with excellent yields and diastereocontrol, was applied to the total synthesis of alkaloids lasubine I and myrtine.

Turn (biochemistry)chemistry.chemical_compoundQuinolizidineStereochemistryChemistryIntramolecular forceOrganic ChemistrySalt metathesis reactionMichael reactionTotal synthesisMoietyPhysical and Theoretical ChemistryBiochemistryOrganicbiomolecular chemistry
researchProduct

The effect of teacher feedback on EFL learners' functional production in classroom discourse.

2005

The present study is based on the analysis of classroom interactions between children and with their teacher both in first and second language contexts. The subjects of our study are two five-year-old classes in an English bilingual school in Madrid, with two different teachers, and one five-year-old monolingual class. The source of our analysis is Halliday’s classification of the communicative functions that children can convey in their mother tongue at the pre-school level (Halliday, 1975). Our premise is that the functional variety of children’s production and their use of language for their own communicative purposes is highly related to both frequency and type of teacher feedback. This…

UNESCO::CIENCIAS DE LAS ARTES Y LAS LETRASMichael Halliday; Educación; Filología inglesaFilologíasEducación:CIENCIAS DE LAS ARTES Y LAS LETRAS [UNESCO]Filología inglesaMichael HallidayOtras filologías modernasFilología
researchProduct