Search results for "metalation"

showing 10 items of 68 documents

Metalation and N-alkylation of some polyamides

1981

Totally N-substituted polyamides were synthesized starting from poly(2,4,4-trimethylhexamethylene terephthalamide) by metalation of the amide groups and subsequent reaction with several electrophiles. Polyamides of this structure are not available from terephthalic acid and the corresponding diamines by polycondensation. This N-alkylation reaction can be used for the synthesis of comb-like graft copolymers. The solubilitity and the thermal properties of these polyamide derivatives are described.

Terephthalic acidMaterials scienceCondensation polymerPolymers and PlasticsMetalationfungiGeneral ChemistryAlkylationCondensed Matter Physicschemistry.chemical_compoundchemistryDiamineAmideElectrophilePolyamidePolymer chemistryMaterials ChemistryOrganic chemistryPolymer Bulletin
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Halogen‐Imparted Reactivity in Lithium Carbenoid Mediated Homologations of Imine Surrogates: Direct Assembly of bis‐Trifluoromethyl‐β‐Diketiminates a…

2020

The selective formal insertion (homologation) of a carbon unit bridging the two trifluoroacetamidoyl chlorides (TFAICs) units is reported. The tactic is levered on a highly chemoselective homologation-metalation-acyl nucleophilic substitution sequence which precisely enables to assemble novel trifluoromethylated β-diketiminates within a single synthetic operation. Unlike previous homologations conducted with LiCH2Cl furnishing aziridines, herein we exploit the unique capability of iodomethyllithium to act contemporaneously as a C1 source (homologating effect) and metalating agent. The mechanistic rationale grounded on experimental evidences supports the hypothesized proposal and, the struct…

Trifluoromethyl010405 organic chemistryIminemetalationGeneral Chemistrycarbenoids; chemoselectivity; homologation; imines; metalation010402 general chemistry01 natural sciencesCombinatorial chemistryCatalysis0104 chemical sciencesCatalysisβ diketiminatechemistry.chemical_compoundDual rolechemistrychemoselectivityiminesHalogenNucleophilic substitutionhomologationcarbenoidsCarbenoidAngewandte Chemie International Edition
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Dirhodium(II) compounds with bridging thienylphosphines: studies on reversible P,C/P,S coordination.

2009

Monocyclometalated compound [Rh(2){(C(8)H(4)S)P(C(8)H(5)S)(2)}(CH(3)CO(2)H)(2)(O(2)CCH(3))(3)] (1 a) and bis-cyclometalated compound [Rh(2){(C(8)H(4)S)P(C(8)H(5)S)(2)}(2)(CH(3)CO(2)H)(2)(O(2)CCH(3))(2)] (2 a) have been isolated from the reaction of dirhodium tetraacetate and tris(2-benzo[b]thienyl)phosphine (2 BTP) using low acidic solutions. By contrast, in pure acetic acid the reaction of Rh(2)(O(2)CCH(3))(4) with 2 BTP and tris(2-thienyl)phosphine (2 TP), followed by replacement of the axial acetate ligands by chlorides, led to [Rh(2){(2-C(8)H(5)S)P(2-C(8)H(5)S)(2)}(2)Cl(2)(O(2)CCH(3))(2)] (3 b) and [Rh(2){(2-C(4)H(3)S)P(C(4)H(3)S)(2)}(2)Cl(2)(O(2)CCH(3))(2)] (5 b), respectively. These n…

TrisStereochemistryMetalationOrganic Chemistrychemistry.chemical_elementGeneral ChemistryCatalysisRhodiumAcetic acidchemistry.chemical_compoundchemistryTriflic acidIsomerizationSodium acetatePhosphineChemistry (Weinheim an der Bergstrasse, Germany)
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A doubly bridged isodicyclopentadienyl zirconium complex: bis{N-(3,5-dimethylphenyl)-N-[(η5-isodicyclopentadien-2-yl)dimethylsilyl]amido-κN}zirconium…

2002

Transmetallation of the dilithium salt of (3,5-dimethyphenylamino)(isodicyclopentadienyl)dimethylsilane by treatment with zirconium tetrachloride in a 2:1 ratio leads to the substitution of all four chloride ligands. With the applied stoichiometry, the title complex, [Zr(C(20)H(25)NSi)(2)].C(4)H(10)O, was obtained and crystallized from diethyl ether. X-ray diffraction characterization showed that both isodicyclopentadienyl ligands (alternatively called 4,5,6,7-tetrahydro-4,7-methano-1H-indene) are complexed to the metal on their exo face in a completely stereoselective manner and that they are eta(5)-bonded to the Zr atom.

ZirconiumDimethylsilaneStereochemistrychemistry.chemical_elementGeneral MedicineCrystal structureMedicinal chemistryGeneral Biochemistry Genetics and Molecular BiologyDilithiumTransmetalationchemistry.chemical_compoundchemistryTetrachlorideStereoselectivityDiethyl etherActa Crystallographica Section C Crystal Structure Communications
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Tuning the Basicity of Synergic Bimetallic Reagents: Switching the Regioselectivity of the Direct Dimetalation of Toluene from 2,5‐ to 3,5‐Positions

2008

Meta-meta metalation: Remarkably, toluene can be directly dimanganated or dimagnesiated at the 3,5-positions using bimetallic bases with active Me3SiCH2 ligands (see scheme, blue). In contrast, n-butyl ligands lead to 2,5-metalation (red). tmp=2,2,6,6-tetramethylpiperidide.

alkali metalsMetalationInorganic chemistrychemistry.chemical_elementManganesemetalationmagnesium010402 general chemistry01 natural sciencesCatalysischemistry.chemical_compoundinverse crown compoundsBimetallic strip010405 organic chemistryRegioselectivityGeneral ChemistryGeneral MedicineAlkali metalCombinatorial chemistryTolueneCommunications3. Good health0104 chemical scienceschemistryReagentmanganeseAngewandte Chemie
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Direct C-H metalation with chromium(ii) and iron(ii): transition- metal host/benzenediide guest magnetic inverse-crown complexes

2009

Check M(etal)ate: The chessboard and the figures represent a special reaction in which different low-polarity metals can metalate arenes directly when they are brought into the right position. In a combination of queen (sodium) and knight (chromium or iron), it is possible for the knight (usually the weaker piece) to make a direct deadly hit on the king (benzene) in this game of elemental chess. Fil: Alborés, Pablo. Johannes Gutenberg Universitat Mainz; Alemania. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Carrella, Luca M.. Johannes Gutenberg Universitat Mainz; Alemania Fil: Clegg, William. University of Newcastle; Reino Unido Fil: García Álvarez, Pablo. Univ…

alkali metalsMetalationchemistry.chemical_elementMineralogyALKALI METALSmetalationCatalysisQueen (playing card)Chromiumchemistry.chemical_compoundironTransition metalCHROMIUMinverse crown compoundsBenzeneIRONOtras Ciencias QuímicasCiencias QuímicasGeneral ChemistryAlkali metalCommunicationsCrystallographychemistrychromiumINVERSE CROWN COMPOUNDSCIENCIAS NATURALES Y EXACTAS
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Combining Neopentyllithium with Potassium tert-Butoxide: Formation of an Alkane-Soluble Lochmann-Schlosser Superbase.

2016

Mixtures of alkyllithium and heavier alkali-metal alkoxides are often used to form alkyl compounds of heavier alkali metals, but these mixtures are also known for their high reactivity in deprotonative metalation reactions. These organometallic mixtures are often called LiC-KOR superbases, but despite many efforts their constitution remains unknown. Herein we present mixed alkali-metal alkyl/alkoxy compounds produced by reaction of neopentyllithium with potassium tert-butoxide. The key to success was the good solubility and temperature-stability of neopentyl alkali-metal compounds, leading to hexane-soluble mixtures, which allowed handling at ambient temperatures and isolation by crystalliz…

chemistry.chemical_classification010405 organic chemistryMetalationPotassiumSuperbasechemistry.chemical_elementGeneral Chemistry010402 general chemistryAlkali metal01 natural sciencesCatalysis0104 chemical scienceschemistry.chemical_compoundchemistryPotassium tert-butoxideAlkoxy groupOrganic chemistryReactivity (chemistry)AlkylAngewandte Chemie (International ed. in English)
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Stereoselective Conjugate Addition of Mixed Organoaluminum Reagents to ?,?-Unsaturated N-Acyloxazolidinones Derived from Carbohydrates.

2005

The stereoselective synthesis of β-branched carboxylic acid derivatives was accomplished by conjugate addition of mixed organoaluminum reagents to chiral α,β-unsaturated N-acyloxazolidinones. Mixed organoaluminum reagentswere generated in situ by transmetalation of Grignard or organolithium compounds with methylaluminum dichloride. Efficient stereocontrol was achieved using different bicyclic glycosamine-derived oxazolidinones, yielding alternatively (R)- or (S)-configured β-branched carboxylic acid derivatives.

chemistry.chemical_classificationAddition reactionTransmetalationchemistryBicyclic moleculeOrganolithium compoundsReagentCarboxylic acidOrganic chemistryStereoselectivityGeneral MedicineConjugateChemInform
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Coordination versatility of pyridine-functionalized N-heterocyclic carbenes: a detailed study of the different activation procedures. Characterizatio…

2005

Three different reaction procedures for the coordination of N-n-butyl-N'-(2-pyridylmethyl)imidazolium salt have produced new N-heterocyclic complexes of Rh and Ir. The direct reaction of the imidazolium salt with [IrCl(cod)](2) provides a NHC-Ir(III)-H complex, while transmetalation from a silver-NHC complex and deprotonation with NEt(3) give new NHC complexes of M(I) and M(III) when reacting with [MCl(cod)](2) or [MCl(coe)(2)](2) (M = Rh, Ir). The crystal structures of the biscarbene Rh(III) and Ir(III) complexes are described. The catalytic properties of the compounds obtained have been tested in the hydrosilylation of acetylenes, the cyclization of acetylenic carboxylic acids, and hydrog…

chemistry.chemical_classificationHydrosilylationSalt (chemistry)Hydrogen transferCrystal structureMedicinal chemistryCatalysisInorganic Chemistrychemistry.chemical_compoundTransmetalationDeprotonationchemistryPyridineOrganic chemistryPhysical and Theoretical ChemistryInorganic chemistry
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The deprotonative metalation of [1,2,3]triazolo[1,5-a]quinoline. Synthesis of 8-haloquinolin-2-carboxaldehydes

2009

New highly functionalized triazoloquinolines were synthesized by applying polar organometallic methods. Double metalation and functionalization provided 3,9-dihalogenated triazoloquinolines. Ring opening of the triazole with loss of nitrogen has been performed for the first time with 3,9-dihalogenated triazoloquinolines allowing the access toward 8-haloquinolin-2-carboxaldehydes under oxidant-free conditions. This approach demonstrates that the triazole ring can be used as protecting group of 2-quinolinecarboxaldehydes, activating the C9-position for lithiation and functionalization by triazole ring opening. 8-Haloquinoline-2-carbaldehydes become in this way readily available.

chemistry.chemical_classificationMetalationOrganic ChemistryQuinolineTriazoleRing (chemistry)BiochemistryCombinatorial chemistryChemical synthesisAldehydechemistry.chemical_compoundDeprotonationchemistryDrug DiscoveryOrganic chemistryProtecting groupTetrahedron
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