Search results for "Organic Chemistry"

Selective favorskii rearrangement in macrocyclic rings

1981

Abstract A mixture of 2,2-dibromo-12-chlorocyclododecanone (IIa) and 2,12-dibromo-2-chlorocyclododecanone (IIb) by Favorskii rearrangement gave selectively methyl 2-chloro-1-cycloundecene-1-carboxylate (IIIa).

Structural and bonding aspects in phosphorus chemistry-inorganic derivatives of oxohaloqeno phosphoric acids

1976

Spektrale eigenschaften und tautomerie aromatischer thiacyclole. Reaktionen mit aktivierten säureamiden. XV

1970

Influence of negative allosteric cooperativity in cation transport.

1992

Abstract The bis-macrocyclic ether5 seems to have a negative allosteric cooperativity and is able to transport double the amount of Na+ and K+ cations as monocyclic systems. This compound could be used as a simple model of the plasma membrane Na+−K+ ATPase which actively pumps Na+ out and K+ into the cell, respectively.

NMR Spectroscopic and quantum chemical characterization of the (E)- and (Z)- isomers of the penta-1,3-dienyl-2-cation

2003

Dilute solutions of the (E )− and (Z )− isomers of pent-1,3-dienyl-2-cations (1) were obtained from reaction of 4-chloro-1,2-pentadiene (2) with SbF5 in SO2ClF/SO2F2 at −135 °C using high-vacuum co-condensation techniques. The experimental NMR spectra of the mixture of the two isomers were compared with quantum chemical 13C NMR chemical shift calculations at HF-SCF, MP2, CCSD and CCSD(T) levels using MP2/tzp geometries. Quantum chemical shift calculations were performed with a tzp basis (9s5p1d/5s3p1d) for carbon and a dz basis (4s/2s) for hydrogen using gauge-including atomic orbitals (GIAOs). The HF-SCF calculations deviate significantly for the positively charged carbon atoms of the ally…

Metal ion-promoted activation of amino acid esters of carbohydrates in the synthesis of peptides

1992

Abstract Carbohydrate esters 1 and 2 of N-protected amino acids are activated by coordination of metal ions and subjected to aminolysis by amino acid esters 3 to form peptides 4 .

THE KINETICS AND MECHANISM OF THE REACTION OF ONIUM CYCLOPENTADIENYLIDES WITH TETRAHALO-p-BENZOQUINONES

1989

Abstract The reaction of triphenylphosphonium cyclopentadienylide (1) with halogen-substituted p-benzoquinones (4) is shown to give a new class of dipolar (zwitterionic) dyes (5) containing phosphorus. The general structure of these molecules has been investigated by a combination of mass spectrometry and multinuclear (7H, 13C and 31P) nmr using the specialist techniques of DEFT spectroscopy, homonuclear (COSY) and heteronuclear 2-D nmr. In addition, stopped-flow (uv/visible) techniques have been used to study the kinetics of the reactions and hence demonstrate that the rate-limiting step is nucleophilic addition of the ylid nucleophile to the quinone, followed by a rapid loss of halide ion…

Preparation and crystal structure of the oxalato-bridged CrIII–AgItwo-dimensional compound {Ag3(H2O)[Cr(dpa)(ox)2]3}n·2nH2O (dpa = 2,2′-dipyridylamin…

2004

The reaction of the mononuclear complex [Cr(dpa)(ox)2]− (dpa = 2,2-dipyridylamine) with Ag+ in aqueous solution affords the two-dimensional compound {Ag3(H2O)[Cr(dpa)(ox)2]3}n·2nH2O (1) whose structure has been determined by single-crystal X-ray diffraction. Six crystallographically independent metal atoms (three chromium and three silver atoms) occur in 1. The three [Cr(dpa)(ox)2]− units in 1 act as ligands towards the silver atoms through the two oxalate groups. Each oxalate group acts as bridging ligand adopting five coordination modes: bis-bidentate, bis-bidentate/monodentate (outer), bis-bidentate/monodentate (inner), bidentate/bis-monodentate (outer) and bidentate/monodentate (outer).…

Reactivity of Distibanes toward Trialkylalanes and -gallanes:  Syntheses and X-ray Structures of Bisadducts and Heterocycles

2001

Reactions between distibanes of the type Sb2R4 and trialkylalanes and -gallanes R‘3M in 1:2 stoichiometry yield eight bisadducts of the type [Sb2R4][MR‘3]2 (R = Me, R‘ = t-Bu, M = Al 1, Ga 2; R = Et, M = Al, R‘ = Me 3, Et 4, t-Bu 5; M = Ga, R‘ = Me 6, Et 7, t-Bu 8), which were characterized by multinuclear NMR studies and elemental analysis. In addition, 1, 2, 5, and 8 are the first structurally characterized neutral main group Lewis acid−distibane bisadducts. 1−8 are unstable in solution toward the formation of heterocycles of the type [R2SbMR‘2]x. [Me2SbGa(t-Bu)2]3 (9) and [Et2SbGa(t-Bu)2]2 (10) have been isolated and their solid state structures determined by single-crystal X-ray diffrac…

Model compound synthesis for the structure determination of new unknown planar aromatic compounds originating from pulp mill

1991

Abstract Several model compounds have been synthesized for verification of the structures of new unknown planar aromatic compounds (UPACs) observed in high-resolution gas chromatography/low-resolution mass spectrometry analyses of the polychlorodibenzodioxins (PCDDs) and polychlorodibenzofurans (PCDFs) in pulp mill products, effluents, sediments and mussels. The mass spectra of synthetic alkyl polychlorodibenzofurans (C6-PCDFs) were different, but those of alkyl polychlorobibenzyls (C5-PCBBs) were very similar compared to the spectra of UPACs.