Search results for "Salt metathesis reaction"

showing 10 items of 49 documents

Interactions of a Diplumbyne with Dinuclear Transition Metal Carbonyls to Afford Metalloplumbylenes

2020

The metathesis reactions of the diplumbyne AriPr6PbPbAriPr6 (AriPr6 = −C6H3–2,6-(C6H2–2,4,6-iPr3)2) with the dinuclear metal carbonyls Mn2(CO)10, Fe2(CO)9, and Co2(CO)8 under mild conditions afforded the complexes Mn(CO)5(PbAriPr6) (1), Fe(CO)4(PbAriPr6)2 (2), and Co4(CO)9(PbAriPr6)2 (3), respectively. Complexes 1–3 were structurally characterized by single-crystal X-ray diffraction and spectroscopically characterized by 1H, 13C{1H}, 59Co{1H}, and 207Pb{1H} NMR; UV–vis; and IR methods. They are rare examples of species formed by the direct reaction of a group 14 dimetallyne with transition metal carbonyls. Complexes 1 and 2 feature Mn–Pb or Fe–Pb single bonds, whereas in 3 a Co–Pb cluster i…

010405 organic chemistryChemistryOrganic ChemistrycarbonylsmetalsMetal carbonylkompleksiyhdisteetorganometalliyhdisteet010402 general chemistry01 natural sciencescobalttransition metals0104 chemical sciencesInorganic ChemistryTransition metalPolymer chemistrySalt metathesis reactionPhysical and Theoretical Chemistrykarbonyylitnuclear magnetic resonance spectroscopy
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Cross-Metathesis/Intramolecular (Hetero-)Michael Addition: A Convenient Sequence for the Generation of Carbo- and Heterocycles

2017

The high stability and functional group compatibility of ruthenium carbene complexes confer them a great ability to catalyze domino processes. For this reason, the combination of metathesis reactions with additional transformations in a domino fashion has been exploited extensively, with the result of expanding the utility of ruthenium carbene complexes beyond that of just olefin metathesis. Among those domino processes, it is worth mentioning the sequence of cross-metathesis/intramolecular Michael addition, which allows for the generation of a wide variety of carbo- and heterocycles in a very simple manner, taking advantage of the benefits of domino reactions. Carbon-, oxygen- and nitrogen…

010405 organic chemistryStereochemistryOrganic Chemistrychemistry.chemical_element010402 general chemistryMetathesis01 natural sciencesCatalysisDomino0104 chemical sciencesRutheniumchemistry.chemical_compoundchemistryNucleophileIntramolecular forceSalt metathesis reactionMichael reactionCarbeneSynthesis
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New approaches to the synthesis of organofluorine nitrogenated derivatives

2004

Fluorinated carboxylic acids are valuable building blocks for several types of organofluorine nitrogenated derivatives. In this review paper, several strategies that use these compounds as starting materials are described. First, fluorinated seven-membered cyclic β-amino esters can be diastereoselectively synthesized from these compounds with a ring-closing metathesis (RCM) reaction as the key step. The use of the RCM reaction in a different approach enables the preparation of fluorinated cyclic α-amino acid derivatives. Fluorinated carboxylic acids also constitute the starting material for the asymmetric synthesis of fluorinated allylic amines. Finally, a solution and solid-phase synthesis…

Allylic rearrangementChemistryOrganic ChemistryEnantioselective synthesisGeneral MedicineMetathesisCombinatorial chemistryBiochemistryInorganic ChemistryRing-closing metathesisSalt metathesis reactionEnvironmental ChemistryOrganic chemistryPhysical and Theoretical ChemistryJournal of Fluorine Chemistry
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General Diastereoselective Synthetic Approach toward Isospongian Diterpenes. Synthesis of (−)-Marginatafuran, (−)-Marginatone, and (−)-20-Acetoxymarg…

2012

This work describes a synthetic approach to the carbocyclic skeleton of isospongian diterpenes that uses the commercially available monoterpene (S)-carvone as a C-ring synthon, which is incorporated into the tetracyclic isospongian framework via a C -> ABC -> ABCD ring annulation strategy using intramolecular Diels-Alder and ring-closing metathesis reactions. This approach has been successfully used to prepare both the title natural isospongians and several nonnatural oxygenated analogues. A preliminary evaluation of the inhibitory activity of the small collection of synthesized isospongians on the mammalian mitochondrial respiratory chain revealed that most were able to inhibit the integra…

AnnulationChemistryStereochemistryMonoterpeneOrganic ChemistrySynthonMolecular ConformationStereoisomerismStereoisomerismRing (chemistry)Mitochondrial respiratory chainIntramolecular forceSalt metathesis reactionDiterpenesThe Journal of Organic Chemistry
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The influence of electron delocalization upon the stability and structure of potential N-heterocyclic carbene precursors with 1,3-diaryl-imidazolidin…

2010

Targeting N-heterocyclic carbenes (NHCs) with increased π-acceptor character featuring N-fluorophenyl substituents, the molecular 2-chloro-1,3-bis(fluorophenyl)imidazolidine-4,5-diones (1a–c) were isolated from the condensation of the corresponding formamidine with oxalyl chloride. These formal adducts of NHCs with hydrogen chloride demonstrated reactivity akin to that of alkyl halides: 1,3,1′,3′-tetrakis(2,6-dimethylphenyl)-[2,2′]diimidazolidinyl-4,5,4′,5′-tetraone (2b) was formed via the reductive coupling of 1b, while 1,3-bis(2,6-diisopropylphenyl)-4,5-dioxoimidazolidin-2-yl acetate (3c) was formed as the result of a metathesis reaction with mercury(II) acetate. Chloride abstraction resu…

ArylN-heterosykliset karbeenitGeneral ChemistryMedicinal chemistryChlorideCatalysischemistry.chemical_compoundOxalyl chloridechemistryImidazolidineHexafluorophosphateElectrophileMaterials ChemistrySalt metathesis reactionmedicineOrganic chemistryN-heterocyclic carbenesCarbenemedicine.drugNew Journal of Chemistry
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Synthesis and biological evaluation of new bicyclic fluorinated uracils through ring-closing metathesis.

2006

Two families of bicyclic fluorinated uracils have been prepared starting from a gem-difluorinated unsaturated nitrile, by means of a ring-closing metathesis reaction to form the new ring, which is fused at the C-5/C-6 or N-1/C-6 positions of the uracil moiety. The selective formation of olefin regioisomers in the metathesis process can be controlled according to the reaction conditions (catalyst, solvent, and temperature). The acaricidal activities of the resulting compounds have also been investigated.

Bicyclic moleculeNitrileMolecular StructureChemistryOrganic ChemistryGeneral MedicineFluorineRing (chemistry)MetathesisChemical synthesisCombinatorial chemistrychemistry.chemical_compoundRing-closing metathesisSalt metathesis reactionOrganic chemistryRing-opening metathesis polymerisationMoietyUracilAcyclic diene metathesisThe Journal of organic chemistry
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Synthesis of Fluorinated and Non-Fluorinated Bicyclic Amidines through Ring-Closing Metathesis

2011

[EN] An efficient method for the synthesis of fluorinated and non-fluorinated imidazoazepines by a ring-closing metathesis reaction as the key step is described. The influence of the fluorine atoms on the preparation of these bicyclic systems is also studied.

Bicyclic moleculeNitrogen heterocyclesOrganic ChemistryAmidineschemistry.chemical_elementMetathesisFluorineMetathesisRing-closing metathesischemistrySalt metathesis reactionFluorineOrganic chemistryPhysical and Theoretical ChemistryAcyclic diene metathesis
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A versatile metathesis reaction for the formation of labile bonds between group 13 and group 15 atoms.

2003

Boron groupMain group elementGroup (periodic table)ChemistryEnvironmental chemistryPolymer chemistrySalt metathesis reactionGeneral ChemistryMetathesisCatalysisAngewandte Chemie (International ed. in English)
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Template Synthesis of Multi-Macrocycles by Metathesis Reactions.

2004

ChemistrySalt metathesis reactionGeneral MedicineTemplate synthesisCombinatorial chemistryChemInform
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Solution-, solid-phase, and fluorous synthesis of beta,beta-difluorinated cyclic quaternary alpha-amino acid derivatives: a comparative study.

2008

The diastereoselective synthesis of cyclic beta,beta-difluorinated alpha-amino acid derivatives bearing a quaternary stereocenter is described. The process relies on the chemo- and diastereoselective addition of allylic organometallic reagents to fluorinated alpha-imino esters and a subsequent ring-closing metathesis reaction (RCM). Complete selectivity in the nucleophilic addition was achieved with (R)-phenylglycinol methyl ether as a chiral auxiliary. The resulting amino acids were introduced into peptide chains, which could facilitate the preparation of potentially bioactive dipeptide derivatives. In addition, the solution synthesis of these cyclic fluorinated alpha-amino acids was succe…

Chiral auxiliaryAllylic rearrangementNucleophilic additionDipeptideMolecular StructureChemistryOrganic ChemistryFluorine CompoundsAmino Acids CyclicEtherEstersStereoisomerismGeneral ChemistryCatalysisStereocenterSolutionschemistry.chemical_compoundSolid-phase synthesisSalt metathesis reactionOrganic chemistryIminesProtonsAminationChemistry (Weinheim an der Bergstrasse, Germany)
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