Search results for "Synthon"

showing 10 items of 50 documents

BENZOTHIETES—VERSATILE SYNTHONS FOR THE PREPARATION OF HETEROCYCLES

1994

Abstract Thermal or photochemical ring opening transforms benzo[b]thiete to o-thiobenzoquinonemethide, a highly reactive 8π electron system. Cycloaddition reactions or linear additions with subsequent cyclizations lead to larger heterocyclic rings. A variety of compounds containing sulfur and possibly further heteroatoms like nitrogen, oxygen or phosphorus in normal, medium and large ring systems can be synthesized on this route.

chemistrySynthonHeteroatomchemistry.chemical_elementRegioselectivityOrganic chemistryStereoselectivityRing (chemistry)SulfurOxygenCombinatorial chemistryCycloadditionSulfur reports
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Improved Preparations of Molybdenum Coordination Compounds from Tetrachlorobis(diethyl ether)molybdenum(IV)

2001

International audience; The reduction of MoCl5 with metallic tin in diethyl ether provides a rapid and convenient entry to [MoCl4(OEt2)2] This compound can be transformed easily and in high yields into a variety of other useful synthons. The loss of ether in the solid state affords a new and reactive form of MoCl4. Treatment with THF, PMe3 or LiOtBu affords [MoCl4(THF)2], [MoCl4(PMe3)3] or [Mo(OtBu)4] in high isolated yields. Treatment with metallic tin in THF affords [MoCl3(THF)3] All of these reactions can be carried out under simple experimental conditions and represent significant improvements relative to previously reported syntheses of the same compounds.

chemistry.chemical_classificationMolybdenumChemistrySynthonchemistry.chemical_elementHalideEtherMedicinal chemistry3. Good healthCoordination complexHalidesInorganic ChemistryMetalchemistry.chemical_compoundSynthetic methodsMolybdenumvisual_artvisual_art.visual_art_mediumOrganic chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistryDiethyl etherTinReduction
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ChemInform Abstract: Preparation and Structural Characterization of (Me3SiNSN)2Se, a New Synthon for Sulfur-Selenium Nitrides.

2010

The reaction of (Me(3)SiN)(2)S with SeCl(2) (2:1 ratio) in CH(2)Cl(2) at -70 degrees C provides a route to the novel mixed selenium-sulfur-nitrogen compound (Me(3)SiNSN)(2)Se (1). Crystals of 1 are monoclinic and belong the space group P2(1)/c, with a = 7.236(1) A, b = 19.260(4) A, c = 11.436(2) A, beta = 92.05(3) degrees, V = 1592.7(5) A(3), Z = 4, and T = -155(2) degrees C. The NSNSeNSN chain in 1 consists of Se-N single bonds (1.844(3) A) and S=N double bonds (1.521(3)-1.548(3) A) with syn and anti geometry at the N=S=N units. The N-Se-N bond angle is 91.8(1) degrees. The EI mass spectrum shows a molecular ion with good agreement between the observed and calculated isotopic distributions…

chemistry.chemical_classificationNMR spectra databaseCrystallographyMolecular geometryDouble bondchemistryPolyatomic ionInorganic chemistrySynthonMass spectrumSingle bondGeneral MedicineNuclear magnetic resonance spectroscopyChemInform
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The [3,3′-Co(1,2-C2B9H11)2]– anion as a platform for new materials: synthesis of its functionalized monosubstituted derivatives incorporating synthon…

2003

[3,3′-Co(8-C5H10O-1,2-C2B9H10)(1′,2′-C2B9H11)] (2) was synthesized by reaction of the caesium salt of [Co(C2B9H11)2]− with dimethyl sulfate in the presence of sulfuric acid as catalyst and tetrahydropyrane as solvent; the zwitterionic compound (2) yielded [3,3′-Co(8-C4H4N-(CH2)5-O-1,2-C2B9H10)(1′,2′-C2B9H11)]− (6), [3,3′-Co(8-C8H6N-(CH2)5-O-1,2-C2B9H10)(1′,2′-C2B9H11)]− (7), and [3,3′-Co(8-C12H8N-(CH2)5-O-1,2-C2B9H10)(1′,2′-C2B9H11)]− (8) through the nucleophilic addition of potassium pyrrolyl, indolyl and carbazolyl, respectively. The nucleophilic addition of the same salts on [3,3′-Co(8-C4H8O2-1,2-C2B9H10)(1′,2′-C2B9H11)] (1) yielded, respectively, [3,3′-Co(8-C4H4N-(CH2)2-O-(CH2)2-O-1,2-C…

chemistry.chemical_classificationNucleophilic additionStereochemistryChemistrySynthonSalt (chemistry)Medicinal chemistryInorganic ChemistrySolventDimethyl sulfatechemistry.chemical_compoundNucleophileIntramolecular forceMoleculeDalton Transactions
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Binding motif of ebselen in solution: Chalcogen and hydrogen bonds team up

2020

Ebselen (2-phenyl-1,2-benzoselenazol-3(2H)one), a glutathione peroxidase mimic, is active against several RNA viruses, among others the retrovirus responsible for the COVID-19 pandemic. In this paper 77Se and 1H NMR studies of ebselen are reported and they identify the chalcogen bond (ChB) and hydrogen bond (HB) that are central in the landscape of interactions formed by the compound in solution. The selenium atom and the hydrogen atom at the C7 carbon act as ChB and HB donors and the O and N atoms of neutral molecules function as acceptors. The ChB and HB give rise to a bifurcated supramolecular synthon, which fastens the interaction acceptor opposite to the N–Se covalent bond of the selen…

chemistry.chemical_classificationStereochemistryEbselenHydrogen bondSynthonSupramolecular chemistryGeneral ChemistryCatalysisdrugssupramolecular chemistrychemistry.chemical_compoundChalcogenchemistrycovid-19Covalent bondMaterials ChemistryThiolMoleculeselenium drugs covid-19 chalcogen bond supramolecular chemistryseleniumchalcogen bond
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Identification of the Iodination and Bromination Products of 3-Hydroxybenzaldehyde: Preparation of 5-Hydroxy-2-iodobenzaldehyde

2017

The monohalogenation products of 3-hydroxybenzaldehyde (1) are useful synthons for the preparation of more complex molecules.1–4 For example, the introduction of a halogen allows the use of a Suzuk...

chemistry.chemical_compound010405 organic chemistryChemistryOrganic ChemistryHalogenSynthonHalogenationOrganic chemistry3-Hydroxybenzaldehyde010402 general chemistry01 natural sciences0104 chemical sciencesOrganic Preparations and Procedures International
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Post-Processing via Cation Exchange Cartridges: Versatile Options

2012

New 68Ge/68Ga radionuclide generators provide the positron emitter 68Ga (T½ = 67.7 min) as an easily available and relatively inexpensive source of a PET nuclide for labeling of interesting targeting vectors. However, currently available “ionic” 68Ge/68Ga radionuclide generators are not necessarily optimized for the routine synthesis of 68Ga-labeled radiopharmaceuticals in a clinical environment. Post-processing of 68Ge/68Ga generators using cation exchange resins provides chemically and radiochemically pure 68Ga with 97±2% within less than 4 min, with 68Ge almost completely removed, and ready for online labeling. This simple, fast, and efficient technology can be extended for new applicati…

chemistry.chemical_compoundCartridgechemistryRadiochemistrySynthonAcetonePositron emittersIonic bondingRadionuclide GeneratorIon-exchange resin
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Tetramethylguanidine (TMG)-catalyzed addition of dialkyl phosphites to α,β-unsaturated carbonyl compounds, alkenenitriles, aldehydes, ketones and imi…

1998

Abstract Tetramethylguanidine-catalyzed addition of dialkyl phosphites to α,β-unsaturated carbonyl compounds, alkenenitriles, aldehydes and ketones constitutes a practical route to a variety of phosphonate synthons. The very mild conditions employed, together with the short reaction times, make the procedure highly versatile and tolerant to a range of functionalities. The proposed methodology is also convenient for the preparation of α-aminophosphonates.

chemistry.chemical_compoundChemistryOrganic ChemistryDrug DiscoverySynthonOrganic chemistryBiochemistryPhosphonateCatalysis
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ChemInform Abstract: The Chemistry of Unsaturated Nitrogen-Heterocyclic Compounds Containing Carbonyl Groups

2010

Publisher Summary Most hydroxy-substituted azaheteroaromatic compounds exist predominately in the NH/carbonyl tautomeric form, and these compounds have been widely discussed. This chapter provides an overview of azaheteroaromatic compounds and I-azetin-4-ones—these are those azaheterocycles that contain in the ring at least one carbonyl group and one or two nitrogen atoms in the form of C=N or N=N bonds. Many of these compounds are unstable but their importance as reactive intermediates is established, and many of them could be used as synthons in the preparation of pharmacologically active compounds. The chapter describes the free existence of I-azetin-4-one and the nucleophilic substituti…

chemistry.chemical_compoundCyclopentadienechemistrySynthonReactive intermediateNucleophilic substitutionCycloheptatrieneOrganic chemistryReactivity (chemistry)General MedicineRing (chemistry)TautomerChemInform
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The Chemistry of Unsaturated Nitrogen–Heterocyclic Compounds Containing Carbonyl Groups

1993

Publisher Summary Most hydroxy-substituted azaheteroaromatic compounds exist predominately in the NH/carbonyl tautomeric form, and these compounds have been widely discussed. This chapter provides an overview of azaheteroaromatic compounds and I-azetin-4-ones—these are those azaheterocycles that contain in the ring at least one carbonyl group and one or two nitrogen atoms in the form of C=N or N=N bonds. Many of these compounds are unstable but their importance as reactive intermediates is established, and many of them could be used as synthons in the preparation of pharmacologically active compounds. The chapter describes the free existence of I-azetin-4-one and the nucleophilic substituti…

chemistry.chemical_compoundCyclopentadienechemistrySynthonReactive intermediateNucleophilic substitutionCycloheptatrieneOrganic chemistryReactivity (chemistry)Ring (chemistry)Tautomer
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