Search results for "Alkoxy group"

showing 8 items of 108 documents

ChemInform Abstract: Palladium-Catalyzed Alkoxy- and Aminocarbonylation of α-Halomethyl Oxime Ethers: Synthesis of 1,3-Alkoxyimino Esters and 1,3-Alk…

2015

The three component reactions of α-bromomethyl oxime ethers, carbon monoxide, and alcohols or aromatic amines give imino esters and amides, respectively.

chemistry.chemical_compoundchemistryAlkoxy groupOrganic chemistrychemistry.chemical_elementheterocyclic compoundsGeneral MedicineOximeCarbonylationCatalysisCarbon monoxidePalladiumChemInform
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ChemInform Abstract: Boron Functionalization of BODIPY by Various Alcohols and Phenols

2014

The synthesis of new B–O BODIPY derivatives functionalized with different alkoxy or diarylalkoxy derivatives is described. These compounds were synthesized from the reaction of different B–F BODIPY precursors with various alcohols and phenols, in the presence of AlCl3. Water-soluble dyes could be synthesized as well with this method, specifically by the introduction of polyethyleneglycol (PEG) groups. A photophysical study of the different compounds was performed, and showed that the B–O BODIPY derivatives exhibit rich fluorescence properties. Finally, the conjugation of the BODIPY core has been extended using two distyryl groups, hence providing NIR emitting BODIPY derivatives, in which on…

chemistry.chemical_compoundchemistryPEG ratioAlkoxy groupchemistry.chemical_elementSurface modificationGeneral MedicinePhenolsBODIPYBoronFluorescenceCombinatorial chemistryChemInform
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Alkoxy-Substituted Hexastyrylbenzenes

2003

Star-shaped compounds 2a–e with a central benzene ring and six p-substituted, (E)-configured styryl groups have been prepared by a sequence of three-fold Heck and three-fold Wittig–Horner reactions. Alkoxy chains (OC3H7, OC6H13, OC10H21, OC12H25) on all six arms guarantee a good solubility of 2a–d, whereas the alternating hexyloxy and cyano substitution in 2e leads to an almost insoluble push-pull system. Irradiation into the long-wavelength absorption of 2a–d (with λmax values of 341–342 nm) results in a statistical photocross-linking, which is characterized by the complete degradation of all stilbene chromophores.

chemistry.chemical_compoundchemistryStereochemistryAlkoxy groupGeneral ChemistryChromophoreAbsorption (chemistry)SolubilityBenzeneRing (chemistry)Medicinal chemistryAdvanced Synthesis & Catalysis
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Eine neue synthese for 3-desoxy-3-iod-zucker über alkoxyphosphoniumsalze

1979

Abstract The alkoxy phosphonium iodides of the 1,2:5,6-di-O-isopropylidene-gluco- and allofuranose are converted to the corresponding 3-iodo sugars without elimination or rearrangement.

chemistry.chemical_compoundchemistryStereochemistryOrganic ChemistryDrug DiscoveryAlkoxy groupPhosphoniumBiochemistryTetrahedron Letters
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Highly Syndiotactic or Isotactic Polyhydroxyalkanoates by Ligand-Controlled Yttrium-Catalyzed Stereoselective Ring-Opening Polymerization of Function…

2017

International audience; Reported herein is the first stereoselective controlled ROP of a specific family of racemic functional β-lactones, namely 4-alkoxymethylene-β-propiolactones (BPL(OR) s). This process is catalyzed by an yttrium complex stabilized by a nonchiral tetradentate amino alkoxy bisphenolate ligand _ONOO(R'2) ₍2-) , which features both a good activity and a high degree of control over the molar masses of the resulting functional poly(3-hydroxyalkanoate)s. A simple modification of the R' substituents in ortho and para position on the ligand platform allows for a complete reversal from virtually pure syndioselectivity (Ps up to 0.91 with R'=cumyl) to very high isoselectivity (Pi…

esteritStereochemistryring-opening polymerizationchemistry.chemical_element010402 general chemistry01 natural sciencesRing-opening polymerizationCatalysisCatalysispolymerointiTacticity[CHIM]Chemical SciencesYttriumpolymeeritta116β-lactonespolymersMolar mass010405 organic chemistryLigand[CHIM.ORGA]Chemical Sciences/Organic chemistrystereoselective catalysisGeneral MedicineGeneral ChemistryYttrium0104 chemical scienceschemistrykatalyysiAlkoxy groupStereoselectivitybeta-lactonesAngewandte Chemie International Edition
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Reaction of 2-acetyltetralone with some esters of benzoic acid

1986

In order to investigate the pharmacological screening of a number of pyran-4-ones their synthesis by cyclization with sulphuric acid of the corresponding 1,3,5-triketones has been carried out with high yields. In the course of preparation of the latter the reaction of 2-acetyltetralone with some esters of benzoic acid derivatives has been studied and in particular, for a number of them, an interesting nucleophilic substitution of a chlorine atom with an alkoxy group on a benzenic nucleus has been evidenced.

inorganic chemicalschemistry.chemical_compoundBicyclic moleculechemistryOrganic ChemistryChlorine atomAlkoxy groupNucleophilic substitutionTriketoneOrganic chemistryAcid hydrolysisSulfuric acidBenzoic acidJournal of Heterocyclic Chemistry
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ChemInform Abstract: Reaction of 2-Acetyltetralone with Some Esters of Benzoic Acid.

1987

In order to investigate the pharmacological screening of a number of pyran-4-ones their synthesis by cyclization with sulphuric acid of the corresponding 1,3,5-triketones has been carried out with high yields. In the course of preparation of the latter the reaction of 2-acetyltetralone with some esters of benzoic acid derivatives has been studied and in particular, for a number of them, an interesting nucleophilic substitution of a chlorine atom with an alkoxy group on a benzenic nucleus has been evidenced.

inorganic chemicalschemistry.chemical_compoundChemistryChlorine atomAlkoxy groupNucleophilic substitutionOrder (group theory)General MedicineMedicinal chemistryBenzoic acidChemInform
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On the mechanism of imine elimination from Fischer tungsten carbene complexes

2016

(Aminoferrocenyl)(ferrocenyl)carbene(pentacarbonyl)tungsten(0) (CO)5W=C(NHFc)Fc (W(CO)5(E-2)) is synthesized by nucleophilic substitution of the ethoxy group of (CO)5W=C(OEt)Fc (M(CO)5(1Et)) by ferrocenyl amide Fc-NH– (Fc = ferrocenyl). W(CO)5(E-2) thermally and photochemically eliminates bulky E-1,2-diferrocenylimine (E-3) via a formal 1,2-H shift from the N to the carbene C atom. Kinetic and mechanistic studies to the formation of imine E-3 are performed by NMR, IR and UV–vis spectroscopy and liquid injection field desorption ionization (LIFDI) mass spectrometry as well as by trapping experiments for low-coordinate tungsten complexes with triphenylphosphane. W(CO)5(E-2) decays thermally i…

tungstenIminemechanism010402 general chemistryPhotochemistry01 natural sciencesMedicinal chemistryReductive eliminationFull Research Paperlcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryAmideNucleophilic substitutionlcsh:Science010405 organic chemistryChemistryOrganic ChemistryferroceneOxidative addition0104 chemical sciencesChemistrycarbene complexesAlkoxy groupPseudorotationlcsh:QimineCarbeneBeilstein Journal of Organic Chemistry
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