Search results for "Oxidative decarboxylation"

showing 6 items of 16 documents

Synthesis of α-aminonitriles using aliphatic nitriles, α-amino acids, and hexacyanoferrate as universally applicable non-toxic cyanide sources

2018

In cyanation reactions, the cyanide source is often directly added to the reaction mixture, which restricts the choice of conditions. The spatial separation of cyanide release and consumption offers higher flexibility instead. Such a setting was used for the cyanation of iminium ions with a variety of different easy-to-handle HCN sources such as hexacyanoferrate, acetonitrile or α-amino acids. The latter substrates were first converted to their corresponding nitriles through oxidative decarboxylation. While glycine directly furnishes HCN in the oxidation step, the aliphatic nitriles derived from α-substituted amino acids can be further converted into the corresponding cyanohydrins in an oxi…

chemistry.chemical_classification010405 organic chemistryCyanideIminiumCyanation010402 general chemistry01 natural sciencesPollution0104 chemical sciencesAmino acidchemistry.chemical_compoundchemistryGlycineEnvironmental ChemistryOrganic chemistryAcetonitrileOxidative decarboxylationAcetone cyanohydrinGreen Chemistry
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Nucleophilic benzoylation using lithiated methyl mandelate as a synthetic equivalent of the benzoyl carbanion. Oxidative decarboxylation of α-hydroxy…

2001

Abstract The synthesis of alkyl aryl ketones using lithiated methyl mandelate as a synthetic equivalent of the benzoyl carbanion is reported (Umpolung). The methodology involves alkylation of methyl mandelate, hydrolysis of the ester group and oxidative decarboxylation of the resulting α-hydroxyacids. The last step is carried out in a catalytic aerobic way using a Co(III) complex in the presence of pivalaldehyde under very mild and advantageous conditions. The procedure is also applied to methyl mandelates substituted on the aromatic ring.

chemistry.chemical_classificationDecarboxylationArylOrganic ChemistryAlkylationBiochemistryMedicinal chemistryUmpolungchemistry.chemical_compoundchemistryNucleophileDrug DiscoveryOxidative decarboxylationAlkylCarbanionTetrahedron
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(S)-Mandelic acid enolate as a chiral benzoyl anion equivalent for the enantioselective synthesis of non-symmetrically substituted benzoins

2011

A strategy for the enantioselective synthesis of non-symmetrically substituted benzoins from (S)-mandelic acid and aromatic aldehydes has been developed. This strategy is based on a diastereoselective aldol reaction of the lithium enolate of the 1,3-dioxolan-4-one derived from (S)-mandelic acid and pivalaldehyde with aromatic aldehydes, which gives the corresponding aldols in good yields. Subsequent hydroxyl group protection as MEM ethers, basic hydrolysis of the dioxolanone ring, oxidative decarboxylation of the α-hydroxy acid moiety, and hydroxyl group deprotection provides chiral non-symmetrically substituted benzoins with high enantiomeric excesses.

chemistry.chemical_classificationDecarboxylationorganic chemicalsOrganic ChemistryEnantioselective synthesisMandelic acidBiochemistryAldehydechemistry.chemical_compoundAldol reactionchemistryDrug Discoverypolycyclic compoundsOrganic chemistryAldol condensationEnantiomeric excessOxidative decarboxylationTetrahedron
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Highly Diastereoselective Arylation of (S)-Mandelic Acid Enolate: Enantioselective Synthesis of Substituted (R)-3-Hydroxy-3-phenyloxindoles and (R)-B…

2005

An easy access to substituted (R)-3-hydroxy-3-phenyloxindoles, (R)-benzylic acids, and benzophenones is described. The reaction of the lithium enolate of the (2S,5S)-cis-1,3-dioxolan-4-one derived from optically active (S)-mandelic acid and pivalaldehyde with several o- and p-halonitrobenzenes proceeds readily to give the corresponding arylation products in good yields and diastereoselectivities. The reduction of the nitro group with Zn/HCl/EtOH in the o-nitro arylation products with concomitant intramolecular aminolysis of the dioxolanone moiety leads directly to enantiomerically pure (R)-3-hydroxy-3-phenyloxindoles. On the other hand the basic hydrolysis of the dioxolanone moiety in all t…

chemistry.chemical_classificationKetoneIntramolecular reactionChemistryOrganic ChemistryNitro compoundEnantioselective synthesisGeneral MedicineMandelic acidChemical synthesisMedicinal chemistryCatalysischemistry.chemical_compoundAminolysisIntramolecular forceNitroOrganic chemistryMoietyOxidative decarboxylationChemInform
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ChemInform Abstract: Nucleophilic Benzoylation Using Lithiated Methyl Mandelate as a Synthetic Equivalent of the Benzoyl Carbanion. Oxidative Decarbo…

2010

Abstract The synthesis of alkyl aryl ketones using lithiated methyl mandelate as a synthetic equivalent of the benzoyl carbanion is reported (Umpolung). The methodology involves alkylation of methyl mandelate, hydrolysis of the ester group and oxidative decarboxylation of the resulting α-hydroxyacids. The last step is carried out in a catalytic aerobic way using a Co(III) complex in the presence of pivalaldehyde under very mild and advantageous conditions. The procedure is also applied to methyl mandelates substituted on the aromatic ring.

chemistry.chemical_classificationchemistry.chemical_compoundNucleophileChemistryArylOrganic chemistryGeneral MedicineAlkylationAlkylOxidative decarboxylationUmpolungCatalysisCarbanionChemInform
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ChemInform Abstract: Catalytic Aerobic Oxidative Decarboxylation of α-Hydroxy Acids. Methyl Mandelate as a Benzoyl Anion Equivalent.

2010

Abstract The monomeric square-planar cobalt(III) complex of bis- N,N ′-disubstituted oxamides catalyses the oxidative decarboxylation of α-hydroxy acids with molecular oxygen/pivalaldehyde with very good yields. This reaction offers an interesting alternative in the use of methyl mandelate as a convenient benzoyl anion equivalent.

chemistry.chemical_compoundMonomerchemistrychemistry.chemical_elementMethyl mandelateGeneral MedicineMolecular oxygenMedicinal chemistryCobaltOxidative decarboxylationCatalysisIonChemInform
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