Search results for "Synthon"

showing 10 items of 50 documents

Total synthesis and evaluation of [18F]MHMZ.

2007

Radiochemical labeling of MDL 105725 using the secondary labeling precursor 2-[(18)F]fluoroethyltosylate ([(18)F]FETos) was carried out in yields of approximately 90% synthesizing [(18)F]MHMZ in a specific activity of approximately 50MBq/nmol with a starting activity of approximately 3GBq. Overall radiochemical yield including [(18)F]FETos synthon synthesis, [(18)F]fluoroalkylation and preparing the injectable [(18)F]MHMZ solution was 42% within a synthesis time of approximately 100 min. The novel compound showed excellent specific binding to the 5-HT(2A) receptor (K(i)=9.0 nM) in vitro and promising in vivo characteristics.

Fluorine RadioisotopesStereochemistryClinical BiochemistryPharmaceutical ScienceBiochemistryBinding CompetitiveRadioligand AssayPiperidinesIn vivoDrug DiscoveryAnimalsRadionuclide imagingReceptor Serotonin 5-HT2ARadionuclide ImagingMolecular BiologyChemistryOrganic ChemistrySynthonTotal synthesisBrainBiological activityRadioligand AssayRatsFluorobenzenesKineticsYield (chemistry)Isotope LabelingSerotonin 5-HT2 Receptor AntagonistsMolecular MedicineSpecific activityKetanserinSerotonin AntagonistsRadiopharmaceuticalsNuclear chemistryBioorganicmedicinal chemistry letters
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Synthesis of No-Carrier-Added 4-[18F]Fluorophenol from 4-Benzyloxyphenyl-(2-thienyl)iodonium Bromide

2011

4-[(18)F]Fluorophenol is a versatile synthon for the synthesis of more complex radiopharmaceuticals bearing a 4-[(18)F]fluorophenoxy moiety. In order to prepare 4-[(18)F]fluorophenol in no-carrier-added (n.c.a.) form only a nucleophilic labelling method starting from [(18)F]fluoride is suitable. In this paper a new, two step radiosynthesis starting from 4-benzyloxyphenyl-(2-thienyl)iodonium bromide and [(18)F]fluoride with subsequent deprotection is described, yielding n.c.a. [(18)F]fluorophenol in 34 to 36% radiochemical yield.

Fluorine Radioisotopespositron emission tomographyTwo stepNo carrier addedPharmaceutical ScienceThiophenesMedicinal chemistryAnalytical Chemistrylcsh:QD241-441chemistry.chemical_compoundOnium CompoundsPhenolsNucleophilelcsh:Organic chemistryBromideDrug DiscoveryMoietyOrganic chemistryPhysical and Theoretical Chemistrydiaryl iodonium saltsCommunicationOrganic ChemistrySynthonRadiosynthesischemistryChemistry (miscellaneous)fluorine-18Molecular MedicineradiosynthesisRadiopharmaceuticalsFluoride4-[18F]fluorophenolMolecules
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Undecylenic acid: A tunable bio-based synthon for materials applications

2016

International audience; An undecylenic acid-based monoglyceride prepared from glycidol and undecylenic acid is used as suitable and tunable synthon for polymerization applications. Epoxidation and acrylation reactions lead to photopolymerizable monomers while transesterification with dimethyl carbonate, metathesis and aminolysis reactions provide access to polyhydroxyurethane-based materials. The successive intermediates were synthesized according to a green chemistry approach implicating solvent-less and catalyzed reactions, and were at each step fully characterized by infrared, 1H and 13C{1H} NMR spectroscopy, elemental analysis and mass spectrometry. Analyses of the resulting polymer mat…

Green chemistryThermogravimetric analysisRenewable resourcesMaterials sciencePolymers and PlasticsOrganic carbonatepolyhydroxyurethanespolyurethanesGeneral Physics and Astronomy02 engineering and technologycyclic carbonates010402 general chemistry01 natural sciences[ CHIM ] Chemical Scienceschemistry.chemical_compoundPolyhydroxyurethanes (PHUs)Aminolysisrenewable building-blockPolymer chemistryMaterials ChemistrymedicineOrganic chemistry[CHIM]Chemical Sciencessolvent-free conditionscastor-oilglycerol carbonatePhotopolymerizationOrganic ChemistrySynthonGlycidolTransesterification021001 nanoscience & nanotechnologyFatty acid0104 chemical scienceschemistryPolymerizationGlycidolpolycarbonatespolymerizationUndecylenic acidderivatives0210 nano-technologymedicine.drug
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Interaction Between Amines and N-Haloimides: a New Motif for Unprecedentedly Short Br...N and I...N Halogen Bonds

2011

The complexes of N-bromosuccinimide or N-iodosuccinimide with a halogen bond acceptor, either 1,4-diazabicyclo[2.2.2]octane (DABCO), hexamethylenetetramine (HMTA) or 1,3,5-triazine (TRZ), led to an unprecedentedly strong (CO)2N–X⋯N halogen bond synthon (X = Br or I) determined from crystal structures of [DABCO]·[NBS]22, [HMTA]·[NBS]22, [TRZ]·[NIS]22 and [HMTA]·[NIS]44. The Br⋯N distances with DABCO and with HMTA donors were 2.347 A and 2.414 A being remarkably shorter (31% and 29%) than the sum of the VDW radii of nitrogen and bromide atoms, respectively. The corresponding I⋯N distances with HMTA and TRZ were 2.549 A and 2.596 A (27.8% and 26.4% less than the sum of the VDW radii of N and I…

Halogen bondChemistryInorganic chemistrySynthonGeneral ChemistryDABCOCrystal structureCondensed Matter Physicschemistry.chemical_compoundCrystallographyBromideHalogenGeneral Materials ScienceHexamethylenetetramineAcetonitrileta116Crystal Engineering Communications
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Modulation of N···I and +N−H···Cl−···I Halogen Bonding: Folding, Inclusion, and Self-Assembly of Tri- and Tetraamino Piperazine Cyclophanes

2010

The acidity of the crystallization conditions was successfully employed in modulating the balance between the robust intramolecular hydrogen bonding (HB) and intermolecular halogen bonding (XB) observed in large tri- (1) and tetraamino (2) piperazine cyclophanes. A careful crystallization of the title XB acceptor cyclophanes with a strong bidentate XB donor 1,4-diiodotetrafluorobenzene (F4DIB) from CHCl3:MeOH, dimethylformamide (DMF), or HCl:H2O:EtOH resulted in X-ray quality crystals of 1·F4DIB, 2@DMF, 2·2@F4DIB, [1H3]Cl3·(F4DIB)6, and [2H6]Cl6·(F4DIB)2. The intramolecular hydrogen bonding pattern in 1 and 2 was retained in neutral protic and aprotic solvents, and regular N−H···N hydrogen …

Halogen bondStereochemistryHydrogen bondSynthonProtonationGeneral ChemistryCondensed Matter PhysicsMedicinal chemistrychemistry.chemical_compoundPiperazinechemistryIntramolecular forceDimethylformamideGeneral Materials ScienceCyclophaneCrystal Growth & Design
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ChemInform Abstract: Tetramethylguanidine (TMG)-Catalyzed Addition of Dialkyl Phosphites to α,β-Unsaturated Carbonyl Compounds, Alkenenitriles, Aldeh…

2010

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.

HydroxylationHydroborationchemistry.chemical_compoundchemistrySilylationSynthonOrganic chemistryGeneral MedicinePhosphonateCatalysisChemInform
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Selektive Synthesen zu 1?-aryl-, 1?-hetaryl-und 1?-alkylsubstituierten 3-Vinylindolen

1987

Selective methods for deriving 1′-aryl-, 1′-indolyl-, 1′-pyrrolyl- and 1′-methyl-substituted 3-vinylindoles2 are described. In all cases the precursors were 3-acylindoles. The new compounds are synthetically useful synthons for annelation of the indole skeleton.

Indole testAnnulationChemistrySynthonOrganic chemistryGeneral ChemistryCombinatorial chemistryMonatshefte f�r Chemie Chemical Monthly
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A convenient synthetic route to useful monobranched polyethoxylated halogen terminated [3,3 -Co(1,2-C2B9H11)2]- synthons

2009

An atom efficient and environmentally friendly route has been developed to obtain a new range of reagents in metallacarborane chemistry having monobranched polyethoxylated cobaltabisdicarbollide synthons. peer-reviewed

Inorganic ChemistryMonobranched polyethoxylated halogenChemistryChemistryReagentHalogenHalogenSynthonOrganic chemistryEnvironmentally friendlyCombinatorial chemistry
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Zirconocene [Cp2Zr] synthon and benzynezirconocene complexes as tools in main group element chemistry

1998

Abstract Interactions between zirconocene or benzyne zirconocene and unsaturated species incorporating main group elements lead to a variety of new metallaheterocycles. Efficient new methodologies of regiospecific syntheses of mono-, bi-, or tricyclic systems incorporating phosphorus, nitrogen, selenium, antimony, germanium or tin are reported.

Inorganic ChemistrychemistryAntimonyMain group elementSynthonMaterials Chemistrychemistry.chemical_elementOrganic chemistryGermaniumPhysical and Theoretical ChemistryTinAryneSeleniumCoordination Chemistry Reviews
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Preparation and structural characterization of (Me(3)SiNSN)(2)Se, a new synthon for sulfur-selenium nitrides.

2002

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…

Inorganic Chemistrychemistry.chemical_classificationNMR spectra databaseCrystallographyMolecular geometryDouble bondChemistrySynthonPolyatomic ionMass spectrumSingle bondNuclear magnetic resonance spectroscopyPhysical and Theoretical ChemistryInorganic chemistry
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