Search results for "enantioselective synthesis"

showing 10 items of 418 documents

ChemInform Abstract: Enantioselective Friedel-Crafts Alkylation of Indoles with (E)-1-Aryl-4-benzyloxybut-2-en-1-ones Catalyzed by an (R)-3,3′-Br2BIN…

2013

A highly enantioselective Friedel–Crafts reaction of unprotected indoles with (E)-1-aryl-4-benzyloxybut-2-en-1-ones catalyzed by a new chiral [Hf{(R)-3,3′-Br2-BINOL}(OtBu)2]2 complex has been developed to functionalize the C-3 position of the indole nucleus with a side chain bearing a 1,4-difunctionalized moiety and a benzylic stereogenic center. The reaction proceeds in good to excellent yields and excellent enantioselectivities (up to 97 % ee). The usefulness of this approach was illustrated with the synthesis of a tryptophol derivative.

Indole testchemistry.chemical_compoundAddition reactionchemistryArylEnantioselective synthesisMoietyGeneral MedicineMedicinal chemistryFriedel–Crafts reactionDerivative (chemistry)StereocenterChemInform
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Enantioselective Friedel-Crafts Alkylation of Indoles with (E)-1-Aryl-4-benzyloxybut-2-en-1-ones Catalyzed by an (R)-3,3′-Br2BINOLate-Hafnium(IV) Com…

2013

A highly enantioselective Friedel–Crafts reaction of unprotected indoles with (E)-1-aryl-4-benzyloxybut-2-en-1-ones catalyzed by a new chiral [Hf{(R)-3,3′-Br2-BINOL}(OtBu)2]2 complex has been developed to functionalize the C-3 position of the indole nucleus with a side chain bearing a 1,4-difunctionalized moiety and a benzylic stereogenic center. The reaction proceeds in good to excellent yields and excellent enantioselectivities (up to 97 % ee). The usefulness of this approach was illustrated with the synthesis of a tryptophol derivative.

Indole testchemistry.chemical_compoundChemistryStereochemistryArylOrganic ChemistryEnantioselective synthesisMoietyRegioselectivityPhysical and Theoretical ChemistryAlkylationFriedel–Crafts reactionStereocenterEuropean Journal of Organic Chemistry
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Synthesis of Functionalized Indoles with a Trifluoromethy-Substituted Stereogenic Tertiary Carbon Atom Through an Enantioselective Friedel-Crafts Alk…

2010

[EN] Chiral complexes of BINOL-based ligands with zirconium tert-butoxide catalyze the Friedel-Crafts alkylation reaction of indoles with beta-trifluoromethyl-alpha,beta-unsaturated ketones to give functionalized indoles with an asymmetric tertiary carbon center attached to a trifluoromethyl group. The reaction can be applied to a large number of substituted alpha-trifluoromethyl enones and substituted indoles. The expected products were obtained with good yields and ees of up to 99%.

IndolesHydrocarbons FluorinatedAlkylationEnonesStereoisomerismAlkylationElectrophilic aromatic substitutionLigandsMedicinal chemistryCatalysisCatalysisStereocenterchemistry.chemical_compoundAsymmetric catalysisOrganic chemistryCombinatorial Chemistry TechniquesAromatic substitutionFriedel–Crafts reactionTrifluoromethylMolecular StructureChemistryOrganic ChemistryEnantioselective synthesisStereoisomerismGeneral ChemistryKetonesCarbonFISICA APLICADAZirconiumFluorinated compounds
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Organocatalytic Enantioselective Friedel–Crafts Aminoalkylation of Indoles in the Carbocyclic Ring

2016

The first general catalytic method for the, so far elusive, enantioselective Friedel−Crafts functionalization of indoles in the carbocyclic ring is presented. This transformation contrasts with the usual tendency of these heterocycles to react at the azole ring. For this purpose, the four regioisomeric hydroxy carbocyclic-substituted indoles were reacted with several isatinderived ketimines, using a Cinchona alkaloid-based squaramide, in a low 0.5−5 mol % catalyst loading, as a bifunctional catalyst. This methodology allows the functionalization of indoles in every position of the carbocyclic ring in a regio- and enantioselective fashion, by switching only the position of the hydroxy group …

IndolesIsatin-derived ketiminesCinchona010402 general chemistryRing (chemistry)01 natural sciencesCatalysisReductive eliminationFriedel−Crafts reactionPhenolsAsymmetric catalysisOrganic chemistryFriedel–Crafts reactionbiologyOrganocatalysis010405 organic chemistryChemistrySquaramideEnantioselective synthesisQuímicaGeneral Chemistrybiology.organism_classification0104 chemical sciencesBifunctional catalystFISICA APLICADAOrganocatalysisACS Catalysis
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Stereoselective Synthesis of Enantiomerically Pure Nupharamine Alkaloids from Castoreum

2009

An animalic note: The first total synthesis of the all-cis nupharamine 2, an alkaloid from beaver castoreum, is based on the stereoselective domino Mannich-Michael reaction of N-galactosylfurylaldimine to give 1 (Piv = pivaloyl), subsequent conjugate cuprate addition, and stereoselective protonation of the enolate. These reactions are all controlled by the carbohydrate. Protonation of the enolate after cleavage of the auxiliary leads to epimer 3.

IndolizidinesIndolizidinesTerpenesChemistryStereochemistryEnantioselective synthesisTotal synthesisRodentiaStereoisomerismProtonationStereoisomerismNupharamineGeneral ChemistryCatalysischemistry.chemical_compoundAlkaloidsPiperidinesAnimalsStereoselectivityEpimerScent GlandsFuransAngewandte Chemie International Edition
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Efficient Stereoselective Synthesis of o-Functionalized P-Chirogenic Phosphines Applied to Asymmetric Catalysis

2015

The stereoselective synthesis of P-chirogenic o-halogenophenylphosphines and their use for the preparation of o-functionalized derivatives are reported. The key step of this synthesis is based on t...

Inorganic ChemistryChemistryOrganic ChemistryEnantioselective synthesisOrganic chemistryStereoselectivityBiochemistryPhosphorus, Sulfur, and Silicon and the Related Elements
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Designing P*-chirogenic Organophosphorus Compounds: from Ligands to Organocatalysts

2015

The interest of organophosphorus compounds bearing chirality on the phosphorus atom has greatly expanded in last decade, due to the development of efficient stereoselective synthetic methods, using...

Inorganic ChemistryChemistryOrganocatalysisPhosphorus atomOrganic ChemistryEnantioselective synthesisOrganic chemistryStereoselectivityChirality (chemistry)BiochemistryPhosphorus, Sulfur, and Silicon and the Related Elements
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Glycosylation-induced asymmetric synthesis: β-amino acid esters via Mannich reactions

2000

Abstract Activation of Schiff bases by N-glycosylation induces asymmetric Mannich reactions with O-silyl ketene acetals to give β-amino acid esters in good yields.

Inorganic Chemistrychemistry.chemical_classificationchemistry.chemical_compoundGlycosylationStereochemistryChemistryOrganic ChemistryEnantioselective synthesisKeteneOrganic chemistryPhysical and Theoretical ChemistryCatalysisAmino acidTetrahedron: Asymmetry
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Supramolecular hydrogen-bonding tautomeric sulfonamido-phosphinamides: a perfect P-chirogenic memory

2011

P-chirogenic, supramolecular hydrogen-bonding C1-symmetrical sulfonamido–phosphinamides (METAMORPhos) have been successfully prepared. They were all found to possess a characteristic prototropic equilibrium between the PIII and the PV tautomers that is slow on the NMR spectroscopic timescale. Despite the dynamic and reversible protonation of the P centre, the P-chirogenic information was found to be retained in the tautomerization process, even in a protic solvent environment. Several strategies to access the corresponding enantiopure compounds were investigated, such as diastereoselective crystallization, or enantioselective synthesis. It was possible to resolve such a class of chiral liga…

Inorganic Chemistrychemistry.chemical_compoundEnantiopure drugchemistryStereochemistryLigandAsymmetric hydrogenationSupramolecular chemistryEnantioselective synthesisProtonationCombinatorial chemistryTautomerProtic solventEuropean Journal of Inorganic Chemistry
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First synthesis of the chiral mixed O/S ligands, 1,2-sulfinyl thiols: application as chiral proton sources in enantioselective protonations of enolat…

2000

Abstract A suitable method for the preparation of the chiral mixed O/S ligands 1,2-sulfinyl thiols is described. These compounds have then been used as a chiral proton source in the enantioselective protonation of 2-methyl tetralone enolate and the results are compared with those obtained from the analogous alcohols. A theoretical model is proposed to explain the different behaviors exhibited in the protonation reaction for each of these proton sources. Configurational assignments for the new chiral thiols have been carried out by means of X-ray analysis.

Inorganic Chemistrychemistry.chemical_compoundProtonchemistryComputational chemistryOrganic ChemistryEnantioselective synthesisTetraloneProtonationPhysical and Theoretical ChemistryNuclear ExperimentCatalysisTetrahedron: Asymmetry
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